National Organic Program (NOP); Strengthening Organic Enforcement, 3548-3627 [2023-00702]
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DEPARTMENT OF AGRICULTURE
Agricultural Marketing Service
7 CFR Part 205
[Doc. No. AMS–NOP–17–0065; NOP–17–02]
RIN 0581–AD09
National Organic Program (NOP);
Strengthening Organic Enforcement
Agricultural Marketing Service,
USDA.
ACTION: Final rule.
AGENCY:
This rulemaking amends the
United States Department of Agriculture
(USDA) organic regulations to
strengthen oversight and enforcement of
the production, handling, and sale of
organic agricultural products. The
amendments protect integrity in the
organic supply chain and build
consumer and industry trust in the
USDA organic label by strengthening
organic control systems, improving farm
to market traceability, and providing
robust enforcement of the USDA organic
regulations. Topics addressed in this
rulemaking include: applicability of the
regulations and exemptions from
organic certification; National Organic
Program Import Certificates;
recordkeeping and product traceability;
certifying agent personnel qualifications
and training; standardized certificates of
organic operation; unannounced on-site
inspections of certified operations;
oversight of certification activities;
foreign conformity assessment systems;
certification of producer group
operations; labeling of nonretail
containers; annual update requirements
for certified operations; compliance and
appeals processes; and calculating
organic content of multi-ingredient
products.
SUMMARY:
DATES:
Effective date: March 20, 2023
Implementation date: March 19, 2024.
FOR FURTHER INFORMATION CONTACT:
Jennifer Tucker, Ph.D., Deputy
Administrator, National Organic
Program. Telephone: 202–720–3252.
Email: Jennifer.Tucker@usda.gov.
SUPPLEMENTARY INFORMATION:
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I. Executive Summary
This rulemaking amends several
sections of the USDA organic
regulations, 7CFR part 205, to
strengthen oversight of the production,
handling, certification, marketing, and
sale of organic agricultural products as
established by the Organic Foods
Production Act of 1990 (OFPA, or ‘‘the
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Act’’).1 When implemented, this
rulemaking will improve organic
integrity across the organic supply
chain, and benefit stakeholders
throughout the organic industry. These
amendments close gaps in the current
regulations to build consistent
certification practices to deter and
detect organic fraud, and improve
transparency and product traceability.
In addition, the amendments will assure
consumers that organic products meet a
robust, consistent standard and
reinforce the value of the organic label.
The need for this rulemaking is driven
by organic market growth and
increasingly complex organic supply
chains. Today’s organic market is
characterized by long—and often
global—supply chains where organic
products are handled by many
businesses before reaching the
consumer. Often, these businesses are
not certified organic—and therefore
have no oversight from the USDA or
USDA-accredited certifying agents. The
absence of direct enforcement over some
entities in the organic supply chain, in
combination with price premiums for
organic products, has created the
opportunity for organic fraud. The
amendments in this rulemaking are
designed to mitigate the occurrence of
organic fraud.
The Agricultural Marketing Service
(AMS) is confident in the integrity and
value of the USDA organic seal.
Consumers can trust the organic label
due to a rigorous oversight system that
operates globally. However, the
challenges of modern organic supply
chains demand action to strengthen
enforcement and uphold the integrity of
the USDA organic label.
This rulemaking strengthens
enforcement of the USDA organic
regulations through several actions
mandated by the Agriculture
Improvement Act of 2018:
1. Reduce the types of uncertified
entities in the organic supply chain that
operate without USDA oversight—
including importers, certain brokers,
and traders of organic products. This
will safeguard organic product integrity
and improve traceability.
2. Require the use of NOP Import
Certificates for all organic products
entering the United States. This change
expands the use of NOP Import
Certificates to all organic products
1 The Organic Foods Production Act of 1990, 7
U.S.C. 6501–6524, is the statute from which the
Agricultural Marketing Service derives authority to
administer the NOP and authority to amend the
regulations as describedin thisrulemaking. This
document is available at: https://uscode.house.gov/
view.xhtml?path=/prelim@title7/chapter94&
edition=prelim
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imported into the United States,
improving the oversight and traceability
of imported organic products.
3. Clarify the NOP’s authority to
oversee certification activities,
including the authority to act against an
agent or office of a certifying agent.
Additionally, certifying agents must
notify the NOP upon opening a new
office, which will allow the NOP to
provide more effective and consistent
oversight of certifying agents and their
activities.
Additionally, this rule includes
several essential actions that work in
alignment with the provisions above to
further strengthen enforcement of the
USDA organic regulations:
1. Require that nonretail containers
used to ship or store organic products
are labeled with organic identity and are
traceable to audit trail documentation.
This information will clearly identify
organic products, reduce the
mishandling of organic products, and
support traceability.
2. Require certifying agents to conduct
unannounced inspections of at least 5%
of the operations they certify, complete
mass-balance audits during annual onsite inspections, and verify traceability
back to the previous certified operation
in the supply chain during annual onsite inspections.
3. Require certifying agents to issue
standardized certificates of organic
operation generated from the USDA’s
Organic Integrity Database (OID); this
will simplify the verification of valid
certificates of organic operation.
Certifying agents must also keep
accurate and current certified operation
data in OID, which will further support
verification of operations’ certified
status.
4. Clarify how certified operations
may submit changes to their organic
system plan, with the goal of reducing
paperwork burden for organic
operations and certifying agents. This
rule also builds consistency in
certification practices by clarifying that
certifying agents must conduct on-site
inspections at least once per calendar
year.
5. Establish specific qualification and
training requirements for certifying
agent personnel, including inspectors
and certification reviewers. Requiring
that personnel meet minimum
education and experience qualifications
and requiring continuing education will
ensure high-quality and consistent
certification activities across all
certifying agents.
6. Clarify conditions for establishing,
evaluating, and terminating equivalence
determinations with foreign government
organic programs, based on an
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for mediation (alternative dispute
resolution).
8. Specify certification requirements
for producer group operations, to
provide consistent, enforceable
standards and ensure compliance with
the USDA organic regulations. Producer
groups must meet certain criteria to
qualify for certification, and must use an
internal control system to monitor
compliance.
9. Clarify the method of calculating
the percentage of organic ingredients in
a multi-ingredient product to promote
evaluation of their organic foreign
conformity systems. This will ensure
the compliance of organic products
imported from countries that have
organic trade arrangements or
agreements with the United States.
7. Clarify that the NOP may initiate
enforcement action against any violator
of the OFPA, including uncertified
operations and responsibly connected
parties; clarify what actions may be
appealed and by whom; and clarify
NOP’s appeal procedures and options
consistent interpretation and
application of the regulation.
10. Require certified operations to
develop and implement improved
recordkeeping and organic fraud
prevention processes and procedures;
require certifying agents to conduct
supply chain traceability audits and to
develop and implement informationsharing processes.
Costs and Benefits
AMS estimates the following costs
and benefits of this rule:
COSTS AND BENEFITS OF SOE RULEMAKING
Average annual cost a
3% Discount
rate
3% Discount
rate
7% Discount
rate
Domestic Costs ................................................................................................
Foreign Costs ..................................................................................................
$10,548,510
8,769,681
$7,884,601
6,550,892
$158,227,651
131,545,210
$118,269,011
98,263,398
Total Costs ...............................................................................................
19,318,191
14,435,494
289,772,861
216,532,409
Benefits .....................................................................................................
32,944,812
24,272,099
494,172,179
364,081,491
a Estimated
b Estimated
annual averages of the 15-year Net Present Value domestic costs discounted at 3 and 7 percent.
total domestic costs for affected industry in Net Present Value discounted at 3 and 7 percent.
Table of Contents
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7% Discount
rate
Total cost b
I. Executive Summary
II. Background
A. Authority
B. Purpose and Need for the Rule
C. History
D. Public Comment
E. Terminology
F. Does this action apply to me?
G. Compliance Date
III. Overview of Amendments
A. Applicability and Exemptions From
Certification
B. Imports to the United States
C. Labeling of Nonretail Containers
D. On-Site Inspections
E. Certificates of Organic Operation
F. Continuation of Certification
G. Paperwork Submissions to the
Administrator
H. Personnel Training and Qualifications
I. Oversight of Certification Activities
J. Accepting Foreign Conformity
Assessment Systems
K. Compliance and Noncompliance
Procedures
L. Mediation
M. Adverse Action Appeal Process
N. Producer Group Operations
O. Calculating the Percentage of
Organically Produced Ingredients
P. Supply Chain Traceability and Organic
Fraud Prevention
Q. Technical Corrections
R. Additional Amendments Considered but
Not Included in This Rule
IV. Regulatory Analyses
A. Summary of Economic Analyses
B. Regulatory Impact Analysis
C. Executive Order 12988
D. Paperwork Reduction Act
E. Executive Order 13175
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F. Executive Order 13132
G. Civil Rights Impact Analysis
H. Related Documents
II. Background
A. Authority
The Organic Foods Production Act of
1990 (OFPA) (7 U.S.C. 6501–6524),
authorizes the Agricultural Marketing
Service (AMS) to establish and maintain
national standards governing the
marketing of organically produced
agricultural products. AMS administers
these standards through the National
Organic Program (NOP). Final
regulations implementing the NOP, also
referred to as the USDA organic
regulations, were published on
December 21, 2000 (65 FR 80548) and
became effective on October 21, 2002.2
Through these regulations, AMS
oversees national standards for the
production, handling, labeling, and sale
of organically produced agricultural
products.
B. Purpose and Need for the Rule
Since full implementation of the
USDA organic regulations, the organic
industry has experienced significant
change. Both demand for and sales of
organic products have risen steadily;
total U.S. sales of organic products
2 7 CFR part 205 National Organic Program; Final
Rule. December 21, 2000. Available on the AMS
website: https://www.federalregister.gov/
documents/2000/12/21/00-32257/national-organicprogram
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reached more than $63 billion in 2021.3
The number of businesses producing,
handling, marketing, and selling organic
products has also grown to meet
consumer demand. Rapid growth has
attracted many businesses to the USDA
organic label and increased the
complexity of global organic supply
chains.
Complexity makes oversight and
enforcement of the organic supply
chains difficult because organic
products are credence goods, which
means that their organic attributes, or
‘‘integrity,’’ cannot be easily verified by
consumers or businesses who buy
organic products for use or resale. The
elements needed to guarantee organic
integrity—transparent supply chains,
trusted interactions between businesses,
and mechanisms to verify product
legitimacy—are more difficult to
achieve in the increasingly complex
modern organic industry. This is further
compounded by inconsistent
interpretation and implementation of
the USDA organic regulations, caused
by a lack of clarity in some portions of
the regulation.
AMS is confident in the integrity and
value of the USDA organic seal.
Consumers can trust the organic label
due to a rigorous oversight system that
operates globally. However, the above
challenges sometimes cause
3 Organic Trade Association, Organic Industry
Survey, 2022.
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mishandling of organic products, where
integrity is compromised due to
improper handling. Additionally, high
demand for organic products, the
absence of direct enforcement over some
entities in the organic supply chain, and
organic price premiums increase the
opportunity and incentive for organic
fraud (when nonorganic products are
deceptively represented as organic).
This rule addresses these risks and
challenges by expanding oversight to
higher-risk portions of organic supply
chains, requiring organic operations to
implement traceability and verification
best practices, and clarifying oversight
and enforcement practices to ensure
more consistent implementation by
certifying agents. This rule will help
prevent loss of organic integrity—which
can occur both through unintentional
mishandling of organic products, and
intentional fraud meant to deceive—and
strengthen the trust consumers, farmers,
and businesses have in the USDA
organic label.
Mishandling of Organic Products and
Complex Supply Chains
One of the most common risks to the
integrity of an organic product is
mishandling—when an entity
unintentionally compromises the
unique attributes that make a product
organic. Once organic integrity is
compromised, that product can no
longer be sold as organic, and both its
unique attributes and price premium are
forfeit. Mishandling can occur at any
point in a supply chain, including
production, handling, transport, storage,
sale, and processing. Examples of
mishandling that can cause a loss of
integrity include exposure to pesticides,
fertilizers, fumigants, or cleaning agents
that are not permitted in organic
production; mixing (‘‘commingling’’) of
organic and nonorganic products;
relabeling or repackaging with incorrect
identification; and inability to
demonstrate organic status due to poor
or incomplete information in records or
transaction paperwork. The likelihood
of such mishandling is greater in long,
complex supply chains where many
businesses, including businesses not
certified organic, handle and sell
organic products.
When the organic regulations were
published in 2000, organic products
were marketed mostly locally or
regionally, and supply chains tended to
be short and transparent; for example,
farm to wholesale to retail to consumer.
Demand and sales have grown
considerably since then. This significant
market growth has attracted more
producers, handlers, product suppliers,
importers, brokers, distributors, and
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others to the organic market. Consider
the example of an organic egg supply
chain in the United States, beginning
with the production of certified organic
corn and ending with the sale of eggs to
the consumer. This demonstrates the
typical entities and transactions in an
organic supply chain under the existing
regulations:
• A certified organic farm produces
organic corn.
• The corn is transported via an
uncertified truck to a local grain
elevator, where it is aggregated with
other organic corn from nearby
producers.
• An uncertified commodity trader
buys the corn.
• The corn is transported via
uncertified truck to an uncertified
storage facility; both transport and
storage are subcontracted and are not
owned by the commodity trader.
• The commodity trader sells the corn
to a certified organic grain supplier; the
two parties remain anonymous because
they use an uncertified broker to
facilitate the transaction.
• The corn is transported via
uncertified rail and river barge to the
grain supplier; it is transloaded and
stored temporarily several times before
being delivered to the certified grain
supplier.
• The certified organic grain supplier
stores the corn and combines it with
imported organic corn purchased from
an importer via an uncertified broker.
• The certified grain supplier sells the
corn to a certified organic feed
processer; the corn is transported via an
uncertified truck.
• The certified processer combines
the corn with several other ingredients
to create organic chicken feed.
• The certified processer sells the
feed to a certified organic egg producer
and transports it via an uncertified
truck.
• The certified organic egg producer
sells organic eggs to an uncertified
distributor.
• The uncertified distributor sells the
organic eggs to a retailer prior to final
sale to the consumer.
This example illustrates the supply
chain for a single ingredient—organic
feed corn. The supply chain for the
organic eggs at the end of this example
is even more complex because it
includes other ingredients that go into
the chicken feed (e.g., soybean meal,
oats, wheat, seed oils). Many of these
ingredients are sourced both
domestically and internationally. Each
ingredient has its own unique supply
chain; together they create a complex
web converging on a single organic
product. It is largely because of this
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complexity that this rule introduces
more specific traceability, verification,
oversight, and enforcement practices for
high-risk portions of organic supply
chains.
Organic Fraud
In addition to mishandling, a growing
risk to organic integrity is fraud—the
deceptive representation, sale, or
labeling of nonorganic agricultural
products as organic. High demand for
organic products, the absence of direct
enforcement over some entities in the
organic supply chain, and organic price
premiums have increased the
opportunity and incentive for organic
fraud. Both NOP and organic
stakeholders have uncovered organic
fraud in organic supply chains,
particularly in organic grain and oilseed
supply chains. Because such supply
chains are complex and involve
multiple changes in ownership of high
demand products, the incentive for
fraud is high. Federal investigations
show that organic grain and oilseed
fraud can lead to tens of millions of
dollars in fraudulent sales within just a
few months. The following examples
highlight some of the types of organic
fraud that this rule seeks to prevent. The
examples also demonstrate the
magnitude of total organic fraud and
how this rule’s additional oversight and
enforcement mechanisms will reduce
fraud.
• In 2019, four individuals were
sentenced to prison terms for their roles
in an organic grain fraud ring. The
charges were brought by the U.S.
Attorney’s Office for the Northern
District of Iowa. All four were sentenced
to prison terms. The lead defendant,
who was sentenced to more than ten
years, pled guilty to defrauding
customers in a scheme involving at least
$142 million in nonorganic grains sold
as organic. The lead defendant sold
fraudulent grain to customers over a
period of seven years, claiming the
product was organically grown in
Nebraska and Missouri.4 This rule
includes more robust traceability and
verification practices that would have
helped identify and stop this type of
fraud earlier, preventing further sale of
the fraudulent products and reducing
the impact of the fraud.
• In February 2020, a federal grand
jury indicted an individual in South
Dakota for allegedly selling $71 million
of nonorganic grains and oilseeds falsely
labeled organic between 2012 and
4 https://www.justice.gov/usao-ndia/pr/fieldschemes-fraud-results-over-decade-federal-prisonleader-largest-organic-fraud.
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2018.5 The defendant pled guilty and
was sentenced in 2021 to 51 months in
federal prison. He was also ordered to
pay more than $15 million in
restitution. The fraud ring spanned
multiple states. After NOP revoked the
business’ organic certifications, the
responsible parties established new
brokerage firms to continue their fraud.
Under the current organic regulations,
these brokerages did not require organic
certification and NOP had no oversight
of their activities. This rule will require
the certification and oversight of brokers
like those involved in this case. This
would allow the NOP to identify and
prevent the fraud, minimizing damage
to the U.S. market.
• In 2017, an investigation revealed
three shipments of imported ‘‘organic’’
corn and soybeans—each weighing
between 36 and 46 million pounds—
were fraudulently labeled as organic.
The associated transaction records
indicated that all three shipments
originated from producers in the Black
Sea region that were not certified
organic, and that the shipments were
originally sold at lower conventional
prices. In one case, a shipment of
soybeans had been fumigated with
aluminum phosphide, which is
prohibited for use in organic production
and handling. By the time this fraud
was discovered, about 21 million
pounds of this same shipment of
soybeans had already been distributed—
primary to organic producers as
livestock feed.6 This rule will require
the use of NOP Import Certificates to
verify the source and integrity of organic
imports, which will help detect and
prevent fraudulently labeled imports,
such as those in this example, from
entering domestic supply chains.
• In July 2022, a Minnesota farmer
was indicted for growing and selling
fraudulent organic grains worth more
than $46 million. The farmer was
certified organic but was growing grains
with synthetic fertilizers and pesticides
in violation of the USDA organic
regulations. He sold this conventional
grain (both what he produced
conventionally as well as conventional
grain he purchased) as organic,
fraudulently presenting his certificate of
organic operation to claim the grain was
organic and withholding the grain’s true
5 https://www.wisfarmer.com/story/news/2020/
02/18/south-dakota-man-indicted-71-millionorganics-fraud/4801207002/. https://
www.justice.gov/usao-sd/pr/florida-man-sentencedconspiracy-commit-wire-fraud-and-moneylaundering.
6 https://www.washingtonpost.com/business/
economy/the-labels-said-organic-but-these-massiveimports-of-corn-and-soybeans-werent/2017/05/12/
6d165984-2b76-11e7-a616-d7c8a68c1a66_
story.html.
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status from buyers.7 This rule includes
more robust traceability and verification
practices that would have helped
identify and stop this type of fraud
earlier, preventing further sale of the
fraudulent products and reducing the
impact of the fraud.
In several of the above examples,
fraudulent livestock feed was sold to
certified organic livestock producers,
magnifying the effects of the fraud. NOP
continues to investigate complaints and
multiple cases of organic fraud at the
production and handling levels. These
examples demonstrate the magnitude of
fraud that NOP intercepts with current
oversight and enforcement techniques.
SOE will significantly bolster the
oversight and enforcement mechanisms
that NOP, certifying agents, and
operations have at their disposal. In the
fraud cases discussed above, these
mechanisms would have allowed earlier
fraud detection and more effective
enforcement action and would have
greatly reduced or even prevented the
fraud.
Patterns in USDA Organic Certification
and Organic Imports
The scope and distribution of
potential organic fraud can also be seen
in changes in the number of operations
certified to the USDA organic standards
and changes in the amount of organic
imports from certain regions. Two
recent NOP efforts show both the
potential type and magnitude of fraud in
the marketplace; more importantly, they
also demonstrate the potential of
improved oversight and enforcement
mechanisms.
In 2018 and 2019, NOP began making
changes to improve oversight of organic
imports, especially grain and oilseed
imports from the Black Sea region. NOP
conducted farm-level yield analysis to
compare expected and actual yield,
supply chain research to better
understand the roles and relationships
of high-risk entities, and targeted import
surveillance to investigate credible
reports of suspected fraud. As a result
of this heightened oversight and
enforcement action, at least 180
operations (60 percent) in the Black Sea
region have lost their organic
certification. In 2016, imports from the
Black Sea region represented 49 percent
of the total dollar value of imported
organic grain and oilseeds (including
corn, soybeans, wheat, barley,
sunflowers, flaxseed, and peas). In 2018,
imports of these grains and oilseeds
from the region had dropped to 21
7 https://www.justice.gov/usao-mn/pr/
cottonwood-county-farmer-charged-46-millionorganic-grain-fraud-scheme.
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percent of the total dollar value. The
steep drop in organic certification and
downward supply trend in the Black
Sea region give an indication of the
magnitude and type of fraud, as well as
the success of stronger oversight and
enforcement strategy. Despite this
enforcement success, key gaps in
oversight remain, such as uncertified
entities in import supply chains and
non-mandatory use of NOP Import
Certificates. This rule will help close
these gaps and bolster NOP’s ability to
detect and prevent fraudulent organic
imports.
In January 2021, AMS announced it
would end its U.S.–India organic
recognition, which had allowed India’s
Agricultural and Processed Food
Products Export Development Authority
(APEDA) to accredit certifying agents to
provide USDA organic certification in
India. AMS ended this recognition
because NOP audits consistently found
India’s organic control system to be
insufficient to protect the integrity of
the USDA organic seal. In late 2020,
prior to the end of U.S.-India
recognition, there were 4,023 operations
certified to the USDA organic standard
in India. Operations formerly certified
by AEDPA-accredited certifying agents
were given an 18-month transition
period to become certified by a USDAaccredited certifying agent. Since the
end of the transition period in July
2022, only 1,471 operations in India
remain certified to the USDA organic
standard. Because failure to become
recertified may indicate an inability to
comply with the USDA organic
regulations, this significant (63 percent)
drop in the number of certified
operations may indicate the general
volume of noncompliant activity
(including mishandling and fraud) that
may have been taking place under the
former recognition. Additionally,
following the end of the U.S. –India
recognition, imports of certified organic
products from India has dropped from
an average per quarter value of $15.6
million to $9.4 million, a 39 percent
decrease. This drop in import value
suggests that a significant number of
organic imports from India may not
have been fully compliant with the
USDA organic standard. The end of the
U.S.-India recognition demonstrates
both the magnitude of potential fraud in
the market, and how more effective
oversight (in this case, certification only
by USDA-accredited certifying agents)
can successfully safeguard the integrity
of the USDA organic label. Despite this
success, there are still gaps in the
oversight of foreign-accredited certifying
agents and imports from these countries.
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This rule will allow NOP to more fully
implement its oversight authority by
codifying specific procedures for
evaluating, accepting, and continuing
equivalency or recognition with foreign
organic programs.
These examples demonstrate how
applying oversight and enforcement best
practices can reduce organic fraud. SOE
will reduce fraud by codifying best
practices in critical areas—exemptions
from certification, import oversight,
traceability, recordkeeping, inspections
and audits, oversight of certifying
agents, and assessment of organic trade
partners. Additionally, the examples
above only show the positive results of
improved oversight and enforcement at
the federal level; SOE will build upon
this success by requiring certifying
agents and organic operations to use
similar techniques. This means proven
oversight and enforcement techniques
will be deployed closer to where fraud
occurs, which will facilitate earlier
detection, stop more fraud before it
cascades further into supply chains, and
more directly deter fraudulent actors.
Because this rule codifies best practices
and requires key parties in organic
supply chains use these practices, AMS
expects that SOE’s benefits will exceed
those demonstrated in the examples
above.
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C. History
In response to their experiences in the
organic system, stakeholders have called
for the NOP to take steps to improve
oversight of organic systems and
enforcement of the USDA organic
regulations. Commonly cited areas for
improvement include certification of
excluded handlers, organic import
oversight, fraud prevention, organic
trade arrangements, and organic
inspector qualifications. Public
discussions on many topics included in
this rule occurred during multiple
National Organic Standards Board
(NOSB) meetings.8
This rule seeks to strengthen
enforcement of the USDA organic
regulations and protect the integrity of
the organic label by (1) strengthening
organic control systems; (2) improving
organic import oversight; (3) clarifying
organic certification standards; and (4)
enhancing supply chain traceability.
AMS identified the need for these
changes through:
8 The April 2021 NOSB meeting is the most
recent example of a public discussion to address
fraud concerns in the organic supply chain. A
discussion document, meeting transcripts, and
public comments are available at https://
www.ams.usda.gov/event/national-organicstandards-board-nosb-meeting-crystal-city-va-0.
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• Direct experience in administering
the NOP, particularly complaint
investigations and audits of accredited
certifying agents;
• The Agriculture Improvement Act
of 2018, 9 which amended the OFPA.
• Recommendations of a 2017 Office
of Inspector General report; 10
• Recommendations of the NOP’s
federal advisory committee, the
National Organic Standards Board
(NOSB); and
• Industry stakeholder and consumer
feedback.
AMS expects the amendments will
bring more effective oversight and
enforcement, improve organic integrity
and product traceability, clarify existing
standards to ensure fair competition,
bolster consumer trust in the organic
label, reduce organic fraud, and support
continued industry growth. Information
about each amendment is described in
more detail below.
D. Public Comment
AMS published the Strengthening
Organic Enforcement proposed rule on
August 5, 2020, opening a 60-day public
comment period. AMS received more
than 1,500 public comments from a
variety of stakeholders, including
certifying agents, certified organic
producers and handlers, uncertified
handlers, retailers, organic inspectors,
trade associations, organic advocates,
scientific organizations, government
organizations, and consumers. The
majority of public comments supported
the proposed amendments and agreed
that the rule is needed to improve
oversight and enforcement, drive
consistent implementation of the
organic regulations, and reduce organic
fraud.
Many stakeholders provided
meaningful feedback about the proposed
policy revisions, including
recommendations to improve the rule
through greater specificity and clarity.
Others discussed how the proposed
amendments would affect them or
suggested alternatives to the proposed
policies. Popular topics of discussion
included the need for certification;
excluded handlers; exemptions from
certification; implementation of the
mandatory NOP Import Certificate
requirements; supply chain traceability
audits; recordkeeping and verification
9 The Agriculture Improvement Act of 2018,
Public Law No: 115–334, is available at: https://
www.congress.gov/115/plaws/publ334/PLAW115publ334.pdf.
10 USDA Office of Inspector General Audit Report
01601–0001–21: National Organic Program
International Trade Arrangements and Agreements.
September 2017: https://www.usda.gov/sites/
default/files/01601-0001-21.pdf.
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requirements; fraud prevention plans for
certified operations; oversight of
producer groups; qualifications and
training requirements for certifying
agent personnel; labeling of nonretail
containers; and unannounced
inspections.
Some comments also discussed the
proposed implementation timeframe of
one year after publication of the final
rule. Some comments asked AMS to
implement the rule immediately, while
others agreed that a one-year timeframe
is reasonable and gives stakeholders
time to comply with the new
requirements. A few comments noted
that some parts of the rule may require
more than one year to implement and
asked AMS to consider this in the final
rule. Few comments addressed the costs
and benefits of the rule in detail, but
many comments noted in general that
the costs of the rule are acceptable and
outweighed by the benefits.
AMS took these public comments into
consideration when revising the policy,
implementation timeframe, and costbenefit analysis of this rulemaking. For
more information on the comments
received and AMS’s response to specific
comments, refer to ‘‘III. Overview of
Amendments.’’
E. Terminology
Throughout this rule, AMS refers to
four concepts—organic integrity,
organic fraud, audit trails, and supply
chain traceability—which are integral to
the purpose of this rule. AMS is
explaining these concepts upfront to
assist reader understanding:
• Organic integrity: The unique
attributes that make a product organic
and define its status as organic. A
product that fully complies with the
USDA organic regulations has integrity,
and its organic qualities have not been
compromised.
• Organic fraud: Deceptive
representation, sale, or labeling of
nonorganic agricultural products or
ingredients as ‘‘100 percent organic,’’
‘‘organic,’’ or ‘‘made with organic
(specified ingredients or food group(s))’’
(7 CFR 205.2).
• Audit trail: Documentation that is
sufficient to determine the source,
transfer of ownership, and
transportation of any agricultural
product labeled as ‘‘100 percent
organic,’’ the organic ingredients of any
agricultural product labeled as
‘‘organic’’ or ‘‘made with organic
(specified ingredients)’’ or the organic
ingredients of any agricultural product
containing less than 70 percent organic
ingredients identified as organic in an
ingredients statement (7 CFR 205.2).
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• Supply chain traceability: The
ability to identify and track the
movement, sale, custody, handling, and
organic status of an agricultural product
along a supply chain. Supply chain
traceability audits are used to verify an
agricultural product’s compliance with
the USDA organic regulations.
F. Does this action apply to me?
You may be affected by this action if
you are engaged in the organic industry.
Potentially affected entities may
include, but are not limited to, the
following:
• Individuals or business entities that
are considering organic certification;
• Existing production and handling
operations that are currently certified
organic under the USDA organic
regulations;
• Brokers, traders, and importers of
organic products that are not currently
certified under the USDA organic
regulations;
• Operations that use non-retail
containers for shipping or storing
organic products;
• Retailers that sell organic products;
• Operations that receive or review
certificates of organic operation to verify
compliance with USDA organic
regulations;
• USDA-accredited certifying agents,
inspectors, and certification review
personnel;
• Operations that import organic
products into the United States; and/or
• Operations that export organic
products to the United States and the
corresponding certifying agents.
This list is not exhaustive but
identifies key entities likely to be
affected by this action. Other types of
entities may also be affected. To
determine whether you or your business
may be affected by this action, you
should carefully examine the regulatory
text and discussion below.
Section
205.2 ...................................
205.100 ...............................
205.101 ...............................
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205.310 ...............................
G. Compliance Date
AMS is establishing a compliance
date for this final rule of March 19,
2024, or 12 months after the effective
date of this final rule. This means that
all entities affected by this rule,
including certified operations and
certifying agents, must comply with the
provisions of this final rule by this date.
This also means that operations
requiring organic certification because
of this final rule must be certified by the
compliance date. AMS is setting this
compliance date to allow affected
entities time to read and understand this
final rule, obtain organic certification if
needed, and prepare for and implement
other changes in this final rule.
III. Overview of Amendments
A. Applicability and Exemptions From
Certification
The table below includes the
regulatory provisions related to this
section of the rule. A discussion of the
policy follows.
Final regulatory text
Terms Defined.
Definitions for Handle, Handler, Handling operation, and Retail establishment.
What has to be certified.
Paragraph (a).
Exemptions from certification.
Entire section.
Agricultural products produced or processed by an exempt operation.
Paragraphs (a) and (b).
The USDA organic regulations require
organic certification of businesses that
sell, process, or package organic
agricultural products as handling
operations. This rulemaking clarifies
that most operations that operate in the
middle of organic supply chains must
be certified organic. This may include
entities that sell, trade, distribute, or
import organic products. The activities
of these operations may affect organic
integrity; therefore, certification is
necessary to assure consumers that
organically produced products meet a
consistent standard. In addition to
clarifying who needs certification, this
rulemaking also provides limited
exemptions to organic certification for
certain entities and activities that
present a low risk to organic integrity.
This action may affect noncertified
operations that handle organic products,
sell organic products, or facilitate the
sale or trade of organic products on
behalf of a seller or oneself; certified
organic operations; organic inspectors;
and certifying agents. Readers should
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carefully examine the regulatory text
and policy discussion to determine if
they are affected.
Background
The organic market has grown
considerably since the USDA organic
regulations took effect in 2002. The
Organic Trade Association reports that
total U.S. organic sales grew from $3.4
billion in 1997 to $61.9 billion in
2020.11 This growth has created
increasingly complex organic supply
chains as additional domestic and
international businesses choose to
produce and sell organic products for
the U.S. market. Some segments of
organic supply chains remain
uncertified under current regulation,
creating gaps in oversight, increasing
the opportunity for fraud, and
complicating enforcement by the USDA
and its enforcement partners.
Oversight and enforcement of organic
supply chains are challenging because
11 Organic Trade Association, Organic Industry
Survey, 2018–2021
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organic products are credence goods,
which means that their organic
attributes, or ‘‘integrity,’’ cannot be
easily verified by an individual.
Guaranteeing organic integrity requires
transparent supply chains, trusted
interactions between businesses, and
mechanisms to verify product
legitimacy. This is best accomplished
via certification, which requires
operations to follow traceability and
verification practices, and provides
regular oversight in the form of audits
and annual inspection. This rulemaking
broadens the scope of who must be
certified, opening more of the organic
supply chain to oversight and mitigating
the risks of noncertified businesses
handling organic product.
OFPA authorizes the USDA to
regulate and enforce the production,
handling, and sale of organic products
(7 U.S.C. 6503). This includes activity
within organic supply chains, from
production through final sale to the
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consumer.12 AMS is exercising its
authority to regulate entities in organic
supply chains by requiring certification
of some types of currently noncertified
operations. This action is mandated by
the 2018 Farm Bill, which states that the
USDA must ‘‘issue regulations to limit
the type of organic operations that are
excluded from certification under
section 205.101’’ of the organic
regulations.13 This rulemaking supports
the OFPA’s purpose ‘‘to assure
consumers that organically produced
products meet a consistent standard (7
U.S.C. 6506(a)(11)).’’
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Who needs to be certified?
Section 205.100(a) of the organic
regulations states that any operation that
produces or handles organic agricultural
products must be certified organic. This
means that operations conducting
activities described in the definition of
handle must be certified organic and
must follow all applicable portions of
the OFPA and the USDA organic
regulations. In general, handle means to
‘‘sell, process, or package’’ organic
agricultural products. Limited
exemptions for operations that handle
organic agricultural products are
described in § 205.101(a)–(h).
The definition of handle includes the
term processing, which is defined in
§ 205.2.14 Operations that process
organic agricultural products must be
certified. Handle further explains what
to ‘‘sell’’ and ‘‘package’’ mean by
including additional examples of
handling activities. The examples
represent typical supply chain activities
that may affect organic integrity. This
includes activities where there is
physical contact with agricultural
products, such as combining,
aggregating, culling, conditioning,
treating, packing, containerizing,
repackaging, labeling, storing, receiving,
or loading.15 Examples of operations
12 OFPA and the USDA organic regulations do not
provide authority to regulate the transport of
organic agricultural products.
13 See section 10104(a) of the Agriculture
Improvement Act of 2018, Public Law No: 115–334,
available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf,
14 7 CFR 205.2 Processing. Cooking, baking,
curing, heating, drying, mixing, grinding, churning,
separating, extracting, slaughtering, cutting,
fermenting, distilling, eviscerating, preserving,
dehydrating, freezing, chilling, or otherwise
manufacturing and includes the packaging,
canning, jarring, or otherwise enclosing food in a
container.
15 The regulations at § 205.2 define ‘‘label’’ and
‘‘labeling’’ to explain the type and location of
information covered. Labeling as a handling activity
refers to the act of applying a label to a product
with an organic claim; applying other types of
labels, such as for inventory or information
accompanying a product, may not need
certification.
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that often conduct these activities may
include grain elevators; bulk grain
handlers; warehouses that cull, label, or
repackage; central bakeries or kitchens
that serve grocery chains; or ports of
entry.
Handle also includes activities where
there may not be physical contact with
agricultural products, such as selling,
trading, facilitating sale or trade on
behalf of a seller or oneself, importing
to the United States, or exporting from
a foreign country for sale in the United
States. These activities are included in
the definition of handle because they
have the potential to affect organic
integrity. Operations that conduct these
activities must be certified (unless
exempt per § 205.101). Examples of
operations that often conduct these
activities may include sales brokers,
commodity traders, ingredient sourcers,
importers, or exporters.
The definition of handle is not an
exhaustive list of activities that must be
certified. There may be additional
activities not listed in the definition that
are similar to the listed activities and
require certification, or different words
or synonyms for the same or similar
activities. The absence of a specific term
in the definition of handle does not
mean the activity is not handling or that
an operation conducting this activity
does not need certification.
What are the certification requirements
for handlers?
All certified organic operations must
follow the portions of the USDA organic
regulations that apply to activities they
conduct. Conversely, some portions of
the regulation will not apply to every
operation (e.g., a certified operation that
only produces crops does not have to
follow the livestock requirements of
subpart C). Similarly, the scope of a
handling operation’s certification only
covers the activities it conducts. For
example, the OSP of a certified importer
would likely describe the operation’s
system to maintain transaction records
and audit trails, verify suppliers and
NOP Import Certificates, and verify
traceability. On-site inspection of such
an operation would likely focus on a
records review and evaluation, rather
than evaluation of physical facilities.
Contractors are sometimes used in the
organic industry to provide services to
certified operations. Contractors that
qualify for an exemption per
§ 205.101(a)–(f) do not need to be
certified. Any contractor performing
handling activities on behalf of an
operation must be certified or described
in the OSP of a certified operation.
It is common for some operations to
handle both organic and nonorganic
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agricultural products (i.e., a split
operation). For a split operation, only
the portion(s) of the operation that
produces or handles organic agricultural
products must be certified. If a portion
of an operation qualifies for an
exemption from certification described
in § 205.101(a)–(h), only that portion
may be exempt, and the remainder of
the operation must be certified if it
produces or handles organic agricultural
products. For example, a grocery store
chain’s retail locations may be exempt
under § 205.101(b) or (c), but its
importing and some distribution
activities would likely need to be
certified.
Organic Agricultural Products Received
From an Exempt Operation
Agricultural products produced or
processed on an exempt operation must
follow all requirements of § 205.310.
This means that an operation receiving
products produced or processed by an
exempt operation cannot represent the
products as certified organic, cannot
display the USDA organic seal on the
products, and cannot use the products
as organic ingredients in a product
produced by the receiving operation. In
effect, product received and then
processed by an exempt operation loses
its certified organic status and cannot be
represented as organic.
However, exempt operations may
perform limited handling of certified
organic products, as described in each
exemption at § 205.101; i.e., if an
exempt operation handles certified
organic products in a manner consistent
with its applicable exemption, the
products maintain their organic status.
This means, for example, that an exempt
warehouse may receive, store, and
prepare for shipment packaged certified
organic products. Conversely, if this
warehouse opens or relabels such
packaged products, then the certified
organic status of the products is lost,
and an operation receiving these
products must not represent them as
certified organic.
The USDA organic regulations require
certified operations to implement
recordkeeping and verification practices
that ensure the integrity of organic
agricultural products they receive,
including products received from
exempt or uncertified operations.
Records must trace organic products
back through any exempt operations to
the last certified operation in the supply
chain, and operations must verify their
suppliers, including exempt operations.
See §§ 205.103(b)(2) and 205.201(a)(3)
in the section on Supply Chain
Traceability and Fraud Prevention later
in this rule.
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Exemptions From Certification
The USDA organic regulations require
certification of any operation that
produces or handles organic agricultural
products (§ 205.100(a)). However, the
regulations provide limited exemptions
to certain types of operations that
conduct low-risk activities, and are
therefore less likely to compromise
organic integrity of the agricultural
products they handle. These
exemptions, and the conditions that
must be met to qualify for each, are
described in § 205.101.
The USDA organic regulations
formerly used the terms ‘‘exemption’’
and ‘‘exclusion’’ to describe activities
that do not require organic certification.
This final rule removes use of the term
‘‘exclusion’’ from § 205.101 and
throughout the organic regulation to
reduce confusion and misinterpretation
about who needs to be certified. The
term ‘‘exemption’’ is now used
exclusively to describe activities that do
not require organic certification.
Previous ‘‘exclusions’’ listed under
former § 205.101(b) have been modified
and are now listed under current
§ 205.101.
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Responsibilities of Exempt Operations
Operations described in § 205.101 are
exempt from the requirement to be
certified organic under subpart E.
However, these exempt operations must
still follow all other applicable portions
of the organic regulations, including the
production and handling requirements
of subpart C. For example, a very small
vegetable farm may be exempt from
certification per § 205.101(a); this means
the farm does not have to be certified
and inspected annually, and does not
have to develop and submit an organic
system plan. However, the farm must
follow the other organic production and
handling requirements of subpart C,
including soil and fertility practices,
crop rotation, weed management, and
seed use practices. Exempt operations
must also comply with § 205.272 and
practices to prevent commingling and
contact with prohibited substances.
Exempt operations must also follow
the applicable labeling requirements of
subpart D. Critically, this means exempt
operations must not represent the
agricultural products they produce or
process as certified organic and must
not use the USDA organic seal.
Additionally, agricultural products
produced or processed by an exempt
operation must not be identified or
represented as organic in a product
processed by another operation (See
§ 205.310, Agricultural products
produced or processed on an exempt
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operation). Additionally, exempt
operations are only permitted to
perform the limited handling activities
described in the applicable exemption;
any handling outside of that described
in the exemption may result in loss of
organic status of products.
Operations that qualify for an
exemption may voluntarily choose to
become certified. By becoming certified,
the operation may market the products
it produces and processes as certified
organic, display the USDA organic seal
on its products, and represent these
products as ingredients for use in other
organic products.
Like certified operations, exempt
operations are subject to penalties for
violating the OFPA and the organic
regulations. Section 205.100(c) of the
organic regulations states that any
person or responsibly connected
person—including exempt operations—
that knowingly sells or labels a product
as organic, except in accordance with
the Act, shall be subject to a civil
penalty as specified in 7 CFR
3.91(b)(1)(xxxvi).16
Recordkeeping by Exempt Operations
Like certified operations, exempt
operations play a critical role in
maintaining the integrity of organic
products as they travel from production
to consumer. Therefore, exempt
operations must maintain records of the
organic products they produce and
handle, including records that:
demonstrate that agricultural products
identified as organic were organically
produced and handled; and verify
quantities of organic agricultural
products received and shipped or sold.
Such records are necessary to maintain
an audit trail for organic products; this
will facilitate many other provisions of
this rule, including supply chain
traceability audits (§ 205.501(a)(21)),
recordkeeping by certified operations
(§ 205.103), on-site inspections
(§ 205.403(d)), and fraud prevention
plans (§ 205.201(a)(3)). Retail
establishments that do not process
agricultural products (see definition for
Handle at § 205.2 and exemption from
certification at § 205.101(b)) do not need
to maintain such records. Exempt
handlers must have required records
available and must show those records
to a representative of the Secretary upon
request. Failure to produce compliant
records may lead to enforcement action.
16 7 CFR 3.91(b)(xxxvi): Civil penalty for
knowingly labeling or selling a product as organic
except in accordance with the Organic Foods
Production Act of 1990, codified at 7 U.S.C.
6519(c). As of the publication of this rule the civil
penalty amount is a maximum of $20,130 per
violation.
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3555
Small Producers and Handlers
Small organic producers and handlers
are exempt from certification at
§ 205.101(a). This exemption is limited
to producers and handlers with gross
agricultural income from organic sales
of no more than $5,000 annually. These
operations are exempt from certification
under subpart E and from submitting an
organic system plan, but must follow all
applicable organic production and
handling requirements of subpart C and
labeling requirements of subpart D. This
includes the requirements to prevent
commingling and prevention of contact
with prohibited substances (§ 205.272).
Such operations must not represent
the agricultural products they produce
or process as certified organic and must
not use the USDA organic seal.
Agricultural products produced or
processed by these exempt operations
must not be identified or represented as
organic in a product processed by
another operation (see § 205.310).
Retail Establishments
Retail businesses that handle organic
agricultural products and sell directly to
consumers may be exempt from
certification. To qualify for an
exemption, the operation must be a
retail establishment and meet the
conditions for the exemptions in
§ 205.101(b) and (c).
The regulations define retail
establishment to include a range of
transaction modes for selling to
consumers that commonly occur in the
modern marketplace. Retail
establishment includes restaurants,
delicatessens, bakeries, grocery stores,
or any retail business with a restaurant,
delicatessen, bakery, salad bar, bulk
food self-service station, or other eat-in,
carry-out, mail-order, or delivery service
of raw or processed agricultural
products. Retail is commonly described
as selling directly to consumers, endusers, or the public. The definition for
retail establishment aligns with that
concept. Businesses which sell to other
businesses (wholesale) do not qualify as
retail establishments. Retail
establishments may use virtual
transactions for sales, but they must also
have a physical location for consumers
to purchase products.
Only operations that are retail
establishments are eligible for the
retailer exemptions. The definitions for
handler and handling operation do not
include final retailers of agricultural
products that do not process agricultural
products. This exemption from
certification is also reinforced at section
205.101(b), which exempts retail
establishments that sell, but do not
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process, organic agricultural products to
consumers.
Section 205.101(c) exempts retail
establishments that process certified
organic agricultural products at the
point of sale to the consumer.
Distributors or brand name owners that
do not qualify as retail establishments
should review the exemptions from
certification at § 205.101(e) and (f), as
those may apply to their activities.
Retail Operations That Don’t Process
Retail establishments that do not
process agricultural products are not
handlers or handling operations and
may be exempt from certification under
§ 205.101(b). The OFPA and § 205.2
define processing as cooking, baking,
heating, drying, mixing, grinding
churning, separating, extracting, cutting,
fermenting, eviscerating, pre-serving,
dehydrating, freezing, or otherwise
manufacturing, and includes the
packaging, canning jarring, or otherwise
enclosing food in a container. A retail
establishment that is not processing may
do other handling activities without
certification. This could include, for
example, removing produce from
shipping boxes and washing and
transferring product to display cases or
opening bags of oats and transferring
contents to bulk food dispensers.
Although a retailer performing such
handling activities may be exempt from
certification, all retail establishments
must comply with § 205.272, which
requires measures to prevent
commingling of organic products and
contact with prohibited substances.
Retail establishments that do not
process ‘‘100% organic’’ and ‘‘organic’’
unpackaged products may use the
USDA organic seal and/or seal of the
certifying agent in retail labeling and
display of these unpackaged products
(§ 205.308). Retail establishments that
do not process ‘‘made with organic. . .’’
unpackaged products may use that
claim in retail labeling and displays
(§ 205.309).
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Retail Establishments That Process
Retail establishments that process
organic agricultural products may be
exempt from certification under
§ 205.101(c). To qualify for this
exemption, a retail establishment must
process organic products at the point of
final sale to the consumer. This means
that the products must be processed and
sold in the same physical location. This
could include repackaging bulk
containers of organic product into
individual units for retail sale within an
individual grocery store or a retail
establishment that prepares ready-to-eat
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meals and sells them online to
consumers from the processing location.
Per § 205.310, organic agricultural
products that are processed by exempt
retail establishments (such as in the
examples above) must not be sold,
labeled or represented as ‘‘certified’’
organic, must not display the USDA seal
or identify the certifying agent, and
must not be used by another operation
as ingredients in a certified organic
product. Only retail establishments that
are certified organic may use the USDA
organic seal (or make certified organic
claims) on products they process.
This exemption does not cover retail
establishments that sell organic
products to consumers which are
processed at a location separate from the
point of sale. This could include, for
example, an online retailer that sells
products processed at an uncertified
facility or a central processing facility
that prepares food sold in bakery and
deli sections of grocery stores. In these
scenarios, the processing facility is not
co-located in the same physical location
as the point of sale and the retail
establishment exemption does not cover
separate processing facilities. The
processors would need to be separately
certified in order for a retail
establishment to sell their products as
organic.
In addition, this exemption does not
cover retailers that process and sell to
consumers only via virtual transactions.
‘‘Virtual transaction’’ describes any form
of transaction that does not occur inperson (e.g., telephone, mail-order, and/
or online sales). Retailers that process
and sell to consumers virtually without
having a physical location for retail
sales must be certified. These businesses
do not meet the definition for retail
establishment, and, by extension, the
conditions for exemption from
certification.
All exempt retail establishments must
comply with the requirements of
§ 205.272, which describes handling
requirements to prevent commingling
and contact with prohibited substances.
In addition, exempt retail
establishments that process organic
products must follow the labeling
provisions specified in § 205.310 and
maintain records to (1) demonstrate that
agricultural products identified as
organic were organically produced and
handled; and (2) verify quantities
received, sold, or produced from such
agricultural products. Exempt handlers
must have these records available and
must show them to a representative of
the Secretary upon request (7 U.S.C.
6519(a)(1)). Failure to produce
compliant records may lead to
enforcement action.
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Operations That Handle Only Products
With Less Than 70 Percent Organic
Ingredients
Section 205.101(d) exempts from
certification operations that only handle
agricultural products with less than 70
percent organically produced
ingredients, and operations that only
identify organic ingredients on the
product informational panel. This
exemption is not new policy. It
combines two existing exemptions:
operations that handle products with
less than 70 percent organic ingredients
(former § 205.101(a)(3)) and operations
that handle products that only identify
organic ingredients on the information
panel (former § 205.101(a)(4)). AMS
combined these exemptions because
they cover operations that handle
products in the same labeling category
(per § 205.305), and because these
operations must follow identical use
and labeling requirements. Operations
that qualify for this exemption are
exempt from certification under subpart
E and from submitting an organic
system plan, but must follow all
applicable organic production and
handling requirements of subpart C and
labeling requirements of subpart D. This
includes the labeling requirements for
products with less than 70 percent
organic content (§ 205.305) and the
requirements to prevent commingling
and prevention of contact with
prohibited substances (§ 205.272).
Handlers covered under this
exemption must have the records
required by § 205.101(i) available and
show them to a representative of the
Secretary upon request (7 U.S.C.
6519(a)(1)). Failure to produce
compliant records may lead to
enforcement action. Such operations
must not represent the agricultural
products they produce or process as
certified organic and must not use the
USDA organic seal. Agricultural
products produced or processed by
these exempt operations must not be
identified or represented as organic in a
product processed by another operation
(see § 205.310).
Storing or Selling Packaged Organic
Products
The movement of packaged and
sealed organic products through the
supply chain is a lower-risk activity.
Packaged products are less likely to be
commingled, exposed to contaminants,
or tampered with, and alterations are
easier to detect. Handling operations
that sell, distribute, or store packaged
organic agricultural products may be
exempt from organic certification. Two
exemptions, at § 205.101(e) and (f),
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apply to limited handling activities
involving only organic agricultural
products that are in sealed, tamperevident packaging or containers. The
key distinctions between these
exemptions are that 205.101(f) covers
operations that buy and sell, in addition
to receiving, storing and/or preparing
for shipment, and that 205.101(f) covers
only retail-packaged products versus
packaged products that are not in final
retail packaging. Tamper-evident
packaging or container means that the
contents are sealed in a manner where
an attempt to break the seal, access the
contents, or reclose the package would
be obvious. These exemptions cover
only the specified handling activities.
These exemptions do not, for example,
cover buying, selling, receiving, storing,
or loading of unpackaged products;
those activities require certification.
The exemption at § 205.101(e) is
intended primarily for storage and
warehouse facilities. Section 205.101(e)
applies to handlers that are only
receiving, storing and/or preparing for
shipment products that are received in
and remain in sealed, tamper-evident
packaging until the products leave their
custody. This allowance may cover, for
example, warehouses and storage
facilities, including some cold storage
facilities that only receive and store
packaged products and prepare them for
shipment to another entity. Examples of
tamper-evident packaging include
produce boxes with ‘‘DO NOT TAMPER
WITH’’ tape placed across the box flaps,
sealed bulk bags of flour, or sealed
drums and totes of olive oil. Storage
facilities or warehouses that receive
products that are not in sealed, tamperevident packaging must be certified.
The exemption at § 205.101(f) is
intended primarily for distributors.
Section 205.101(f) applies to handlers
that only buy, sell, receive, store and/or
prepare for shipment retail-packaged
organic agricultural products. This
allowance may cover, for example, some
distributors, brand name owners, and
sales brokers that purchase and/or
receive products in their finished retail
packaging. Products must be received in
and remain in the final retail packaging
without alteration throughout their
custody. This exemption does not apply
to sales brokers, traders, or other
handlers that buy and sell products that
are not in their final retail packaging.
Preparing for shipment is an activity
that is covered under both exemptions
at § 205.101(e) and (f). This may include
various tasks that must be performed
with the sealed, tamper-evident
packaging remaining intact and without
altering product contents or any retail
labeling. Examples of preparing for
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shipment include putting packaged
products into shipping containers,
applying internal tracking numbers,
shrink-wrapping shipping cartons to a
pallet, breaking down pallets of fully
packaged products, adding protective
packaging to nonretail containers or
retail displays of organic products,
packing individual packaged products
onto a shipping pallet, loading/
unloading packaged products onto or
from transport vehicles, and placing
individual retail packages into a retail
display which the certifying agent of the
last certified handling operation has
verified as compliant.
Handlers that qualify for an
exemption at § 205.101(e) or (f) must use
practices for preventing commingling
and contamination of organic products,
in compliance with § 205.272. In
addition, exempt handlers must have
records available and must show those
records to a representative of the
Secretary upon request, to show that
organic products are organically
produced and handled and to verify
quantities of organic product received
and shipped or sold. Failure to produce
compliant records may lead to
enforcement action.
Customs Brokers
Section 205.101(g) exempts Customs
brokers from organic certification.
Customs brokers facilitate the entry of
products into the United States by
helping meet import documentation and
filing requirements and by acting as
intermediaries between importers and
the U.S. government. Customs brokers
do not take ownership or physical
possession of organic products and their
actions present minimal risk to organic
integrity. They are often distinct from
sales or commodity brokers, who sell or
facilitate the sale of organic products—
those operations must be certified if
they handle organic products. Customs
brokers also play a critical role by filing
NOP Import Certificate data in the U.S.
Custom and Border Protection’s (CBP)
Automated Commercial Environment
(ACE) import entry system.
This exemption is limited to Customs
brokers as defined by 19 CFR 111.1: ‘‘a
person who is licensed under this part
to transact customs business on behalf
of others.’’ Customs business is further
defined in 19 CFR 111.1 and includes
‘‘activities involving transactions with
CBP [U.S. Customs and Border
Protection] concerning the entry and
admissibility of merchandise . . .
payment of duties, taxes, or other
charges . . . the preparation . . . of
documents in any format and the
electronic transmission of documents
. . . intended to be filed with CBP in
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3557
furtherance of any other customs
business activity . . . ’’ 17
To qualify for this exemption,
Customs brokers must only conduct
customs business. If a Customs broker
conducts any additional activity within
the definition of handle—such as
selling, importing, or trading—the
Customs broker must be certified.
Logistics Brokers
Section 205.101(h) exempts from
certification operations that only
arrange for the shipping, storing,
transport, or movement of organic
agricultural products. Sometimes
known as ‘‘logistics brokers,’’ these
operations facilitate the movement and
storage of agricultural products by
connecting a consigner (or consignee)
with a carrier who can transport/store
the products. Logistics brokers do not
take ownership or physical possession
of organic products. The activities they
conduct present minimal risk to organic
integrity because they only secure
transport/storage to meet the needs of a
third party who owns or is responsible
for the agricultural product.
This exemption is limited to
operations that only arrange for the
shipping, storing, transport, or
movement of agricultural products and
do not conduct any other activity in the
definition of handle. If such an
operation conducts other handling
activities—such as selling, importing, or
trading—the operation must be certified.
Transport
Transport of agricultural products
alone is not a handling activity and does
not require certification (see definitions
of handle in 7 CFR 205.2 and 7 U.S.C.
2502(8)). Transport generally refers to
the movement of products in commerce.
Examples of activities which are
transportation and do not require
certification include: moving organic
hay or milk from a certified producer to
a certified organic buyer or certified
processing facility, moving organic grain
or organic livestock from certified
organic farms to a certified handling or
slaughter facility, and food delivery
services transporting prepared foods
from a retail establishment to a
consumer.
Any activities other than the
movement of product on a
transportation vehicle or moving
products between transportation
17 See 19 CFR 111.1 for complete definitions of
Customs broker and Customs business: https://
www.ecfr.gov/cgi-bin/retrieve
ECFR?gp=&SID=ab6e30
d35ef538ce07bc8021d6e1d4c3
&mc=true&n=sp19.1.111.a&r=SUBPART
&ty=HTML#se19.1.111_11.
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Federal Register / Vol. 88, No. 12 / Thursday, January 19, 2023 / Rules and Regulations
vehicles (transloading) are handling and
require certification. Handling activities
which are adjacent to transport require
certification unless they are covered by
exemptions 205.101(e) or (f) for
packaged products. Examples of
adjacent activities which do not qualify
as transport include combining,
splitting, containerizing, packing/
repacking, treating, sorting, opening,
enclosing, or labeling/relabeling. In
addition, loading or unloading of
unpackaged products into or from a
storage facility is not a form of
transportation; this activity must be
certified.
Certified operations are responsible
for verifying that products handled by
uncertified entities in their supply chain
remain in compliance with the organic
regulations. This includes verifying
organic products transported by an
uncertified transporter. A certified
operation needs to describe procedures
for verifying suppliers in the supply
chain and the organic status of products
received (§ 205.201(a)(3)). In addition,
certified operations must maintain
records back to last certified operation,
which may encompass uncertified
operations that fall between certified
entities (§ 205.103(b)(2)). The certified
organic operation responsible for the
organic products that are transported
must: maintain records, for the audit
trail and traceability, in sufficient detail
as to be readily understood and audited;
demonstrate prevention of commingling
and contamination during
transportation (§ 205.272); fully describe
the transportation practices in the
organic system plan; and ensure that the
transportation records for organic
products are available for inspection.
Certified operations that load or receive
products from uncertified transporters
can verify prevention of contamination/
contact with prohibited substances
through, for example, affidavits or other
documentation of vehicle clean out.
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Summary of Changes to the Final Rule
AMS made several revisions to the
proposed regulatory text when writing
this rulemaking. Changes to the
rulemaking are discussed below. This is
then followed by responses to specific
themes from public comment.
• AMS revised the definition of
handle to include additional examples
of activities that require organic
certification. AMS added these activities
in response to public comments, which
asked for additional clarity about who
must be certified. The additional
activities in the definition more clearly
indicate activities that require
certification and will help businesses
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determine whether they need organic
certification.
• AMS simplified the term handler
and removed ‘‘except for operations that
are exempt from certification’’ and ‘‘or
a portion of [an operation]’’ from
handling operation. These phrases are
redundant because they are explained in
§ 205.100—What has to be certified.
AMS also added ‘‘except final retailers
of agricultural products that do not
process agricultural products’’ to both
definitions. This clarifies that certain
final retailers are not handlers or
handling operations and aligns the
definitions with OFPA. The two
definitions are now mostly
synonymous, differing only in their
reference to either a person or an
operation.
• The proposed rule would have
replaced the defined term retail food
establishment with the updated term
retail operation, which focused on the
key activities of retailers, notably those
selling ‘‘directly to final consumers.’’
Many public comments noted that the
proposed phrase ‘‘direct to final
consumers’’ was imprecise and would
not be interpreted consistently by
stakeholders. These comments also
indicated that stakeholders are familiar
with the meaning of the original defined
term retail food establishment and how
to apply it. Therefore, this final rule
uses the defined term retail
establishment, which has language very
similar to the original retail food
establishment, to ensure consistent
stakeholder understanding. This final
defined term removes the word ‘‘food’’
because retailers sometimes sell nonfood items; it also avoids the potentially
confusing phrase ‘‘directly to final
consumers.’’ Finally, this definition for
retail establishment adds more
examples of types of retail
establishments to help stakeholders
determine whether they are a retail
establishment.
• AMS removed ‘‘or a portion of an
operation’’ from the descriptions of each
exemption; this language was redundant
because it is included in § 205.100—
What has to be certified.
• AMS removed references to
§ 205.272 because they are redundant to
the reference to subpart C in the
introductory paragraph of § 205.101.
• In the introductory paragraph of
§ 205.101, AMS replaced references to
§ 205.310 with a reference to subpart D.
This more broadly references the
labeling requirements exempt
operations must follow, including use of
the USDA seal and labeling in retail
environments.
• In § 205.101(b), AMS removed
‘‘sells’’ to clarify that retail
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establishments may also perform some
handling (not just selling) in the regular
course of business.
• In § 205.101(c), AMS removed the
reference to agricultural products
‘‘previously labeled for retail sale’’ and
replaced it with the statement ‘‘certified
under this part’’ to clarify that retailers
may process certified organic products
regardless of whether the products are
labeled for retail sale or for other use
(e.g., organic products labeled for food
service).
• AMS revised § 205.101(e) to exempt
only storage of products sealed in
tamper-evident packaging. Storage of
unpackaged organic products is a highrisk activity that requires certification to
maintain integrity. Sealed, tamperevident packaging makes organic
products less susceptible to fraud and
mishandling and helps maintain organic
integrity during storage and handling by
uncertified operations.
• AMS added new paragraph (f) in
§ 205.101 to exempt the sale of retail
products sealed in tamper-evident
packaging. Sale of this type of packaged
retail products presents little risk to
organic integrity, and operations storing
and selling these products do not
require organic certification.
• AMS added new paragraphs (g) and
(h) to § 205.101 to exempt Customs
brokers and logistics brokers because
these operations only facilitate entry of
imports into the United States, and their
activities do not present a risk to organic
integrity.
• AMS removed recordkeeping
requirements from specific exemptions
and replaced them with a general
‘‘Recordkeeping by exempt operations’’
paragraph at § 205.101(i).
• AMS revised § 205.310 to remove
‘‘or excluded’’ and replaced ‘‘handled’’
with ‘‘processed’’ to more clearly
indicate that products processed by an
exempt operation must not be used as
an ingredient in an organic product
processed by others.
Summary of Public Comment
AMS received many public comments
from stakeholders across the organic
industry discussing this section of the
proposed rule. The majority of
comments generally supported AMS’s
proposed revisions and agreed that the
organic regulations must clearly
indicate who needs to be certified and
reduce the types of uncertified
operations in organic supply chain.
Many commenters requested further
clarification of the proposed changes,
particularly about the need for organic
certification and exemptions from
certification.
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Revised Definitions
The revised definition of handle was
discussed in many comments. Some
commenters requested expanding the
definition to include terms such as
‘‘port,’’ ‘‘transload,’’ and ‘‘brand owner’’
to the regulatory text. Commenters also
requested specific distinctions be made
between ‘‘transport’’ and ‘‘transload,’’
noting current inconsistency in how
these are interpreted by the industry.
Some comments discussed further
clarification needed, including how
‘‘cold storage’’ fits into the rule. Other
comments requested to further clarify
handle by better defining ‘‘split.’’
Another commenter requested
clarification for operations that
repackage or repurpose certified organic
products for on-site sale (e.g., delis). A
few commenters also requested AMS
discuss virtual transactions more
clearly.
In response to AMS’s request for
additional activities that may need to be
certified, commenters suggested the
following be added to the definition of
handle: split, open, close, sort, combine,
consolidate, aggregate, enclose,
condition, treat, size, grade, transload,
brand ownership, private label, import,
export, commingle, transport, and
deliver.
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Exemptions
Certification of and exemption for
brokers was frequently discussed in
comments. Many commenters requested
that brokering activities be exempt, with
some requesting broad exemptions for
all brokers and others favoring
exemptions for certain brokering
activities. These comments explained
that exemptions are warranted because
brokers typically do not take physical
possession of the products. Many
commenters also stated that all
brokering activity should be certified,
regardless of physical or financial
possession.
Several comments requested changes
or clarifications to the exemption for
operations with organic sales of less
than $5,000, although the proposed rule
did not revise existing policy. Most of
these comments wrote in support of this
exemption, though some proposed
changes such as raising the maximum
receipts to $10,000 while still
maintaining exempt status.
In general, some comments requested
fewer exemptions, and asked AMS to
implement a transition period for
operations that would require
certification under the rulemaking.
Further comments wrote that operations
that sell direct to consumers should be
eligible for exemption. Several
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comments requested that storage
facilities which only receive product
packaged by a certified operation be
exempt. One comment requested that
products, not operations, be eligible for
exemption because operations can
interact with organic and non-organic
products.
Some comments also requested
clarification about private label brands.
There was no clear consensus among
comments about the need to certify such
operations. Many comments stated that
these operations must be certified, and
that doing so would improve
traceability and integrity. Others
requested that private labels be exempt
to avoid additional costs and labeling
inconsistencies. Further comments
requested that ‘‘private label’’ be added
to the definition of ‘‘retail
establishment’’ because retail brands
often sell private-labeled product.
Comments disagreed about the
specific requirements exempt operations
must follow. Some comments argued for
more specific regulatory requirements
for exempt operations (i.e., clarify what
exempt operations can and cannot do).
Many comments discussed the use of
the USDA organic label by exempt
operations, stating that exempt
operations should not be permitted to
use the certified organic label. They
requested that whenever the organic
label is used, the business must be
certified.
Transport
Many comments requested specific
exemptions for most transportation of
organic products. Specifically, several
comments requested that milk hauling
and transportation between two
certified operations should be exempt
from certification. While the majority of
comments requested these types of
transportation be exempt, some
comments disagreed, requesting limits
on transportation exemptions. Other
comments requested clarification for
whether third-party delivery services
that restaurants use are exempt. Finally,
some comments also asked AMS to
clarify whether transloading activities
need to be certified.
Recordkeeping and Compliance
Some comments were concerned with
verifying exempt operations
compliance. Several commenters
suggested requiring universal use of
affidavits when doing business with
exempt operations. Another suggested
utilizing invoices to track compliance
using mass-balance audits.
Many comments addressed
recordkeeping. Several comments
requested modifying recordkeeping
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requirements to require exempt
operations to maintain records for five
years to align requirements for certified
and exempt operations. Other comments
wrote that the recordkeeping
requirements are burdensome for
exempt businesses and asked AMS to
not require certain recordkeeping
practices.
Responses to Public Comment
Definition of Handle
(Comment) AMS received many
comments about the definition of
handle and activities that should or
should not require certification.
Comments discussed a wide range of
activities spanning all segments of the
supply chain and suggested many
additional activities to include in the
definition of handle, including to split,
open, close, sort, combine, consolidate,
aggregate, enclose, condition, treat, size,
grade, transload, brand ownership,
private label, import, export,
commingle, transport, and deliver.
Conversely, comments also provided
examples of activities that should not
require certification, including storing
packaged products, transporting,
delivering, repackaging or splitting
cases of retail-packaged products,
loading, receiving, brokering, selling or
trading packaged products, selling retail
products, or labeling for inventory
purposes.
(Response) AMS agrees that some of
the activities presented by commenters
require certification and has added more
examples to the definition of handle to
help clarify who and what activities
must be certified. The definition of
handle is not an exhaustive list of
activities that must be certified. There
may be additional activities not listed in
the definition that require certification,
or different words or synonyms for the
same or similar activities. The absence
of a specific term in the definition of
handle does not mean the activity is not
handling or that an operation
conducting this activity does not need
certification. More specific responses to
certain activities are discussed below.
(Comment) Several comments noted
the difference between the definitions of
handler and handling operation and
asked AMS to either clarify this
difference, or harmonize the two
definitions.
(Response) AMS simplified handler
and removed ‘‘except for operations that
are exempt from certification’’ and ‘‘or
a portion of [an operation]’’ from
handling operation. These phrases are
redundant because they are explained in
§ 205.100—What has to be certified.
AMS also added ‘‘except final retailers
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of agricultural products that do not
process agricultural products’’ to both
definitions. This clarifies that certain
final retailers are not handlers or
handling operations, and aligns the
definitions with OFPA. The two
definitions are now mostly
synonymous, differing only in their
reference to either a person or an
operation.
(Comment) Several comments asked
AMS to include importing and
exporting to the definition of handle,
noting that the mandatory use of NOP
Import Certificates requires certification
of importers and exporters.
(Response) AMS agrees with these
comments and has added importing to
the United States and exporting for sale
in the United States to the definition to
help clarify that these activities require
certification, and to support the
mandatory use of NOP Import
Certificates described in Section 2 of
this rule, Imports to the United States.
(Comment) Commenters questioned
the inclusion of ‘‘facilitating sale or
trade’’ in the definition for handle. The
comments explained that the meaning is
vague and too broad and would result
in customs brokers, freight forwarders,
sales brokers, and administrative
activities requiring certification.
(Response) The original definition for
handle covered many activities in the
supply chain, from post-production to
retail sale. The updated definition is
specific about which activities are
included in ‘‘sell, process or package.’’
However, the list of activities is not
exhaustive and does not capture all
activities that may be considered as
selling, processing, or packaging an
agricultural product. AMS included
‘‘facilitating sale or trade on behalf of a
seller or oneself’’ as a general category
to capture activities which are integral
to selling a product and may be known
by various names. The definition for
handle includes handling activities that
fall under AMS’s authority, although
sometimes certain activities listed in
handle may not require certification.
For example, entities that perform lower
risk activities—such as Customs
brokers, logistics providers (e.g., freight
forwarders), and limited handling of
packaged products—may be exempt
from certification (see § 205.101(e)—
(h)).
Retail
(Comment) AMS received comments
requesting clarification regarding
whether distribution centers and
transport vehicles associated with a
retail establishment are exempt from
certification. Some commenters
requested that off-site warehouses and
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distribution centers not be exempt
unless they meet proposed § 205.101(e).
According to commenters, this
clarification is needed to ensure that
distribution centers do not avoid
certification by claiming to be an
exempt retail establishment.
(Response) A warehouse or
distribution center associated with a
retail establishment is only exempt if it
meets the criteria described in
§ 205.101(e) or (f). Transport vehicles
associated with a retail establishment do
not require certification if they only
transport and do not handle organic
agricultural products per § 205.2.
(Comment) AMS received comments
asking whether virtual transactions with
a final consumer are exempt from
certification. Although a few comments
asked NOP to either exempt or require
certification of this activity, most
comments did not give an opinion and
only asked NOP for clarification.
(Response) AMS has provided
additional clarification by noting that
only businesses that meet the definition
for retail establishment are exempt
under § 205.101(b) and (c). Virtual
businesses that only sell retail packaged
products to consumers, but do not
qualify as retail establishments, may be
exempt from certification if they meet
the criteria of § 205.101(f). AMS
provides further detail in the ‘‘Retail
establishments’’ section of the preamble.
(Comment) Comments noted that the
proposed definition of retail operation
did not include the list of examples that
was provided in the preamble, and
asked AMS to add them to the
definition.
(Response) AMS agrees that the
examples help clarify the definition and
has added them to the final definition
of retail establishment.
(Comment) Comments requested
revising the exemption for retailers that
process by not limiting this to
processing only products that were
previously labeled for retail sale.
Comments indicated that retailers
commonly source products labeled for
food service.
(Response) AMS has removed that
qualification from § 205.101(c) to clarify
that exempt retail establishments may
process certified organic products
regardless of whether the products are
labeled for retail sale.
(Comment) AMS received comments
asking about the status of food delivery
services, specifically those affiliated
with or serving retail operations.
Although a few comments asked NOP to
either exempt or require certification of
this activity, most comments did not
give an opinion and only asked NOP for
clarification.
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(Response) Services which deliver
products from a retail establishment to
a consumer may not require
certification. A service which delivers
product from the retailer to the
consumer after final sale and does not
engage in handling is transport and does
not require certification.
(Comment) Comments requested
clearer guidance on what handling
activities retail operations could engage
in and remain exempt. Comments
explained that the exemption for
retailers that only sell and retailers that
process creates uncertainty for the many
retail operations that sell and handle. A
few comments gave specific examples of
activities that exempt retail
establishments should be allowed to
conduct, including removing/unpacking
products, washing and transferring
products to retail displays, and breaking
down master cases of individual
packaged products. However, most
comments did not give an opinion and
only asked NOP for clarification.
(Response) AMS has revised the
definitions of handler and handling
operation to exclude retailers that do
not process organic agricultural
products; these operations may not
require certification. This is reinforced
by the exemption for retailers that
handle but do not process at
§ 205.101(b), which acknowledges that
exempt retail establishments may
perform some handling activities. AMS
has also revised the definition for
handle to be more specific about the
types of activities included. The
additional description will help to
clarify the differences and overlap in
handling and processing activities.
(Comment) Comments asked to clarify
the meaning of ‘‘point of sale’’ in
reference to virtual transactions for
retailers. There was a suggestion to
allow virtual transactions only when the
sale occurs from a brick-and-mortar
retail location, to prohibit retailers that
sell only via an online platform.
(Response) The definition for retail
establishment allows for virtual retail
transactions. For a retail establishment
to be exempt, the sales must occur at the
same location as the processing, and
there must also be a physical location
for consumers to purchase products.
Storage
(Comment) AMS received comments
stating that storage of unpackaged or
bulk organic products is high-risk and
should require certification. They also
noted that the proposed rule eliminated
the distinction between packaged and
unpackaged product relating to
receiving, storing, and loading activities;
this could allow high-risk operations
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such as grain elevators and ports of
entry to be exempt from certification.
Some comments requested AMS only
exempt the storage of sealed, tamperevident packaged products.
(Response) AMS has revised the
exemption at § 205.101(e) to exempt
only operations that store, receive, and
prepare for shipment organic products
in sealed, tamper-evident packages.
Products must remain in their packages
and the exempt operation must not
handle the product beyond storing,
loading, and preparing for shipment.
Operations that store bulk products or
products not packaged in sealed,
tamper-evident packaging must be
certified.
AMS made this change because the
proposed rule would have exempted
operations that store unpackaged or
bulk organic products. Many public
comments noted that storage of
unpackaged organic products is a highrisk activity that requires certification to
maintain integrity. AMS agrees that
storage of unpackaged products is a
high-risk activity. Lack of sealed or
protective packaging increases the
likelihood of contamination with
prohibited materials (e.g., pesticides and
fumigants), commingling with
nonorganic products, and
misidentification. These risks are
especially great in high-activity areas,
and storage of unpackaged products
requires additional care and oversight to
ensure organic integrity is maintained.
Therefore, AMS is requiring
certification of operations that store
unpackaged products. Conversely,
because packaging reduces the risk of
contamination, commingling, and
misidentification, AMS is granting an
exemption from certification for
operations that only store packaged
products that are sealed upon arrival
and remain in their packaging.
AMS has narrowed the exemption to
include only operations that store,
receive, and/or prepare for shipment
organic products in sealed, tamperevident packaging. Sealed, tamperevident packaging makes organic
products less susceptible to fraud and
mishandling and helps maintain organic
integrity during storage and handling by
uncertified operations.
(Comment) Commenters requested
AMS exempt from certification
activities where packaged product
remains in its container, such as
breaking up pallets of packaged organic
products that remain in its original
inner packaging, or placing such
products into a retail display.
(Response) Section 205.101(e) and (f)
exempt operations that receive, store,
and prepare for shipment organic
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products enclosed in sealed, tamperevident packages or containers.
Preparing for shipment may include
various tasks that must be performed
with the sealed, tamper-evident
packaging remaining intact and without
altering product contents or any retail
labeling. Examples of preparing for
shipment include putting packaged
products into shipping containers,
applying internal tracking numbers,
shrink-wrapping shipping cartons to a
pallet, breaking down pallets of fully
packaged products, adding protective
packaging to nonretail containers or
retail displays of organic products,
packing individual packaged products
onto a shipping pallet, placing
individual retail packages into a retail
display, and loading/unloading
packaged products onto or from
transport vehicles.
(Comment) Several comments asked if
cold storage of organic agricultural
products is exempt from certification,
pointing to the inclusion of ‘‘chilling’’
in the definition of processing.
(Response) Cold storage of organic
agricultural products may be exempt
from organic certification if the activity
meets the criteria of § 205.101(e), i.e.,
only sealed, tamper-proof packaged
organic products are stored. The act of
cooling packaged organic products is a
common low-risk storage activity that is
different from ‘‘chilling’’ performed as
part of organic product processing.
(Comment) Several commenters
requested that AMS remove the verb
‘‘loads’’ from proposed § 205.101(e) for
operations that storage organic products,
arguing that ‘‘load’’ could be conflated
with handling activities such as placing
or packaging bulk products into
containers.
(Response) AMS uses ‘‘prepare for
shipment’’ in exemptions at
§ 205.101(e)–(f) to clarify that these
exempt operations may not perform
activities such as packaging or loading
bulk products into containers. Prepare
for shipment means that these
operations may move products into or
onto a mode of transport, provided that
the products are packaged per
§ 205.101(e)–(f).
(Comment) One commenter asked
AMS to require certification of storage
facilities that store both organic and
nonorganic agricultural products. They
argue that such ‘‘split’’ storage
operations are a known source of
contamination and commingling, and
that certification is necessary to prevent
this.
(Response) This rulemaking addresses
the risks of contamination and
commingling by split storage operations
by (1) requiring the certification of
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operations that handle unpackaged
organic products and (2) limiting the
exemption for storage operations to only
those that handle sealed, tamper-proof
packaged organic products. AMS
believes these changes will mitigate the
risks of split operations.
Additionally, § 205.100(a) states that
‘‘each operation or portion of an
operation’’ that handles organic
agricultural products must be certified.
Similarly, the exemption at § 205.101(e),
which allows storage of packaged
organic products without certification,
would be limited to only the portions of
an operation that meet the narrow
criteria of this exemption. This means
that a portion of a split operation that
stores unpackaged organic products
needs to be certified.
Transport
(Comment) Commenters requested
that AMS explicitly state what
transportation activities are exempt
from certification. They also noted that
the regulatory text and preamble lack a
specific exemption for transport of
agricultural products.
(Response) The OFPA provides AMS
authority to regulate the handling (i.e.,
selling, processing, or packaging) of
organic agricultural products; however,
transportation activities are not
included in this authority. Transport is
generally described as the movement of
products in commerce. Based on the
OFPA, transport of organic agricultural
products does not need to be certified;
however, any handling activities that
occur during transport must be. See the
definition of handle for examples of
activities that may require certification.
(Comment) AMS received several
comments asking if milk haulers will
require organic certification. Most
comments requested only clarification
on this topic, but several specifically
requested that milk haulers be exempted
from certification.
(Response) AMS is defining the need
for certification based on activities
performed, not type of business, because
this will ensure that businesses
conducting high-risk activities require
certification (and conversely that
businesses that conduct low-risk
activities remain exempt). A milk hauler
would be exempt from certification if
they only transport organic milk (e.g.,
move milk from a dairy to a processor)
but do not otherwise handle the milk
(e.g., process or package loads of milk).
Transport alone does not require
certification.
(Comment) AMS received comments
requesting that the transport exemption
be limited to transport from one
certified operator to another, or to a
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final retailer, to ensure traceability of
product throughout supply chains.
(Response) AMS is not restricting
transport of organic agricultural
products from one certified operation to
another. This rule ensures traceability
via other means: certified operations
must maintain audit trail
documentation for products they
produce or handle (§ 205.103(b)(3)) and
keep records to trace organic products
received back to the last certified
operation in the supply chain
(§ 205.103(b)(2)). This means that
certified operations must ensure
traceability of products transported by
uncertified operations, including if
several uncertified transporters are used
in sequence.
(Comment) Many comments
discussed transloading organic
agricultural products and asked AMS to
clarify if this activity requires
certification.
(Response) Transloading is commonly
defined as the movement of agricultural
products between modes of transport.
AMS does not have the authority to
regulate transport. Therefore,
transloading strictly between modes of
transportation does not need to be
certified.
However, transloading is sometimes
used to describe the movement of
agricultural products from storage to
transport or transport to storage. AMS
considers these activities to be loading
and receiving (see § 205.2 and the
definition of handle). Moving
unpackaged organic agricultural
products from storage to transport, or
from transport to storage, requires
certification. If the organic agricultural
products are enclosed in sealed, tamperproof containers or packages, then
loading and receiving is exempt from
certification.
Small Operations
(Comment) Several comments
discussed the exemption for small
operations at § 205.101(a). A few
commenters asked AMS to clarify if the
exemption applies to both production
and handling operations. Others
requested that AMS allow ingredients
produced or processed by such exempt
operations to be used as certified
organic ingredients produced by other
operations. One commenter requested
AMS increase the gross sales limit of
$5,000.
(Response) This rulemaking does not
modify current policy regarding the
exemption for small operations. Section
205.101(a) exempts operations that
produce or handle agricultural products
as ‘‘organic’’ but whose gross
agricultural income from organic sales
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totals $5,000 or less annually. However,
these operations must not sell, label, or
represent agricultural products they
produce or process as certified organic,
and such products must not be used as
certified organic ingredients in products
processed by another operation (see
§ 205.310). Additionally, the $5,000
gross sales threshold is set by the OFPA,
and AMS does not have authority to
increase this limit.
Selling and Representing
(Comment) Many comments
requested that AMS provide exemptions
for operations that do not physically
handle or contact organic agricultural
products, arguing that such operations
do not threaten organic integrity.
(Response) AMS disagrees with
commenters’ claim that lack of physical
contact equals low risk. Organic
integrity depends on oversight and
transparency across the entire organic
supply chain—including some
operations that may never physically
contact organic products. The need for
certification is based on risk and this
rule requires certification of high-risk
operations such as importers, traders,
and others that facilitate the sale of
organic products. Although these
operations may not physically contact
organic products, they control critical
events along organic supply chains
where organic integrity can be
compromised, including purchase, sale,
transport, storage, and combining or
splitting products. For example, an
importer, broker, or trader could
unintentionally compromise the
integrity of organic products they buy or
sell by not seeking or keeping records to
demonstrate traceability and verify
organic integrity. Without these records,
there is no way to verify that a product
was properly handled by the multiple
physical handlers in a supply chain. A
breach of integrity could go unreported,
and the importer or trader would
unintentionally sell a product that has
lost its organic status and integrity.
Similarly, brokers and traders could
mistakenly direct contracted storage
facilities and transporters to perform
activities that compromise organic
integrity, such as directing a storage
facility to fumigate a container of
organic wheat or directing a transporter
to combine loads of organic and
nonorganic corn.
Additionally, because importers,
brokers, traders and others that facilitate
sales have direct financial interest in the
transaction of organic products, they
have the incentive and opportunity to
commit fraud. For example, an
operation could falsify records to claim
that a nonorganic product is certified
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organic, or direct a contracted storage
facility or transporter to mix organic and
nonorganic products, and then claim the
entire load is organic. NOP has
investigated many notable cases of fraud
committed by uncertified operations
that did not physically contact the
products in question (see the discussion
on fraud under ‘‘Purpose and Need for
the Rule’’).
The risk of both unintentional breach
of integrity and fraud has grown with
the organic market as supply chains
increase in complexity and more
uncertified parties affect control of
organic products and their transaction.
Requiring certification based on risk
ensures traceability, verification,
accountability, and oversight at the most
critical points of the supply chain,
including the activities of brokers,
traders, importers, and others who
facilitate sale but may not physically
contact organic products. The rule also
provides reasonable exemptions for lowrisk operations to reduce cost and
administrative burden to the industry.
(Comment) Many comments
discussed private labeling and brand
ownership of organic products.
Opinions differed about the need to
certify these operations. Some
commenters argued that requiring
certification of these operations would
improve transparency and traceability of
products, while others claimed that
doing so would be unnecessary and
create potential problems with labeling
and traceability.
(Response) ‘‘Brand owners’’ or
operations that sell or distribute organic
products produced by another operation
on their behalf may be exempt from
certification if they meet the criteria of
§ 205.101(f). This exemption allows the
buying, selling, receiving, storing, and
preparing for shipment of organic
products that are packaged for retail
sale. The products must be sealed in
tamper-evident packaging ready for
retail sale, and the operation must not
open or otherwise handle the retail
packages. Private labeling operations
that process organic agricultural
products must be certified.
(Comment) Commenters asked AMS
to clarify if sales brokers need to be
certified, including businesses that buy
or sell only packaged organic products.
(Response) Operations that sell, trade,
or facilitate sale or trade of organic
agricultural products on behalf of a
seller or oneself must be certified.
However, AMS is providing an
exemption for operations that only buy,
sell, receive, store, or prepare for
shipment organic products packaged for
retail sale (§ 205.101(f)). The products
must be sealed in tamper-evident
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packaging labeled for retail sale, and the
operation must not open or otherwise
handle the retail packages. Sale of
organic products not packaged for retail
sale (e.g., bulk; unpackaged; packaged
for nonretail sale; unsealed, non-tamperevident packaging) must be certified.
Supply Chain Logistics
(Comment) Many comments asked
AMS to provide a specific exemption for
Customs brokers licensed by U.S.
Customs and Border Protection, arguing
that these operations only facilitate
entry of imports into the United States,
and that their activities do not present
a risk to organic integrity.
(Response) AMS agrees that the
activities of Customs brokers do not
threaten organic integrity. Therefore,
§ 205.101(g) exempts from certification
licensed Customs brokers that only
conduct Customs business per 19 CFR
111.1. This exemption is limited to
Customs business; other activities
conducted by a Customs broker that fall
within the definition of handle—
including selling, importing, or trading
organic agricultural products—may
require certification.
(Comment) Several comments asked
AMS to clarify if businesses that
facilitate the storage and transport of
organic agricultural products, such as
logistics brokers and freight forwarders,
require certification.
(Response) Logistics brokers, freight
forwarders, and other businesses that
facilitate storage and transport of
agricultural products may be exempt if
they meet the criteria of §§ 205.101(e) or
(h). These exemptions only apply to
operations that conduct or facilitate
specific shipping, storing, or transport
activities. This may include logistics
brokers or freight forwarders who do not
take ownership or physical possession
of organic products and only provide a
service by connecting a consigner (or
consignee) with a carrier who
transports/stores the products.
Additionally, transport of organic
agricultural products does not require
certification if the transport operation
does not handle the products (see
definition of handle in § 205.2). Other
handling activities—such as selling,
importing, or trading—must be certified.
(Comment) Many commenters
responded to AMS’s request for
comment about ports of entry. Most
commenters agreed that the activities of
ports—such as loading, storing,
receiving, combining, and splitting—
must be certified if unpackaged
products are being handled. Comments
stated that handling of unpackaged
goods at ports should be certified
because ports conduct physical
activities that can compromise organic
integrity. Ports unload, move, split,
combine, and store both organic and
nonorganic products, increasing the risk
of commingling organic and nonorganic
products, and the risk of contamination
with substances not allowed in organic
handling. In contrast, several comments
from trade associations state that
requiring certification of port activities
may cause delays, increase costs, and
may have limited positive impacts on
organic integrity. Several comments
asked AMS for more clarification about
the need for ports of entry to be
certified.
(Response) Ports of entry must be
certified if the activities they conduct
meet the definition of handle and do not
clearly fit an exemption at § 205.101(a)–
(h).
Recordkeeping and Verification
(Comment) Several comments noted
that proposed § 205.101 did not clearly
explain the requirements and
recordkeeping practices each exempt
operation must follow. A few comments
also asked AMS to increase the
recordkeeping requirement for exempt
operations to five years to be consistent
with requirements for certified
operations.
(Response) AMS has revised § 205.101
to clarify the requirements and
Section
205.2 ...................................
205.273 ...............................
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205.300 ...............................
recordkeeping practices that exempt
operations must follow. Specific
references to individual requirements
are removed from each exemption, and
the introductory paragraph explains
universally that all exempt operations
must follow the applicable production,
handling, and labeling requirements of
subparts C and D. The preamble further
explains with specific examples of
requirements exempt operations may
have to follow.
AMS has also removed recordkeeping
requirements from individual
exemptions and replaced them with a
single, consistent recordkeeping
requirement that applies universally to
most exempt operations. AMS retained
the requirements for exempt operations
to maintain records for at least three
years because there was not a
compelling reason for increasing that
timeframe without prior notice.
(Comment) AMS received several
comments asking who is responsible for
verifying exempt operations’
compliance with the organic
regulations.
(Response) Certified operations are
responsible for verifying the compliance
of the certified organic products they
receive, including those received from
exempt operations. Section
205.201(a)(3) requires a certified
operation’s OSP to include monitoring
practices and procedures to verify
suppliers (including exempt suppliers)
and the organic status of products they
receive. AMS is not prescribing how
certified operations should verify
suppliers and products; this provides
flexibility for operations to develop and
implement practices that best suit their
business and the products they handle.
B. Imports to the United States
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms Defined.
Definitions for Organic exporter and Organic importer.
Imports to the United States.
Entire section.
Use of the term, ‘‘organic.’’
Paragraph (c).
Purpose, Scope, and Authority
AMS is amending the USDA organic
regulations by adding a new section
(205.273) requiring the use of the
National Organic Program Import
Certificate (‘‘NOP Import Certificate’’).
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The NOP Import Certificate is a
transaction certificate, or data set, that
contains detailed information about the
quantity and origin of organic product
being imported into the United States.
Any organic agricultural product
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imported to the United States must be
associated with a valid NOP Import
Certificate, generated by the certifying
agent of the final certified exporter
sending the product to the United
States.
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The purpose of the NOP Import
Certificate is to document the organic
status and quantity of imported organic
products as they travel from a certified
organic exporter in a foreign country to
a certified organic importer in the
United States. The NOP Import
Certificate ensures an auditable business
transaction by documenting that the
products in the shipment are organic
and may be sold, represented, and
distributed as organic within the United
States.
The mandatory use of NOP Import
Certificates is authorized by the Organic
Foods Production Act (OFPA), as
amended by the ‘‘2018 Farm Bill’’.18
The OFPA specifies what information
an NOP Import Certificate must include
(7 U.S.C. 6502(13)) and also stipulates
that the NOP Import Certificate must
‘‘be available as an electronic record’’
and captured in a tracking system
maintained by the U.S. Government (7
U.S.C. 6514(d)). The OFPA also
provides the Secretary with broad
authority to establish appropriate and
adequate enforcement procedures and
any other requirements that the
Secretary may determine to be necessary
(7 U.S.C. 6506).
The NOP Import Certificate must be
presented to U.S. Customs and Border
Protection (CBP) through the CBP
Automated Commercial Environment
(ACE). The use of this standardized
electronic format will ensure
consistency in data for auditing,
surveillance, and enforcement purposes.
The OFPA, as amended by the 2018
Farm Bill, states that AMS must
establish a system of tracking NOP
Import Certificates, and that AMS ‘‘may
integrate the system into any existing
information tracking systems for
imports of agricultural products’’ (7
U.S.C. 6514(d) and 6522(c)).19
Because the OFPA enables AMS to
access information available in ACE (7
U.S.C. 6521(c)), AMS is using ACE to
accept NOP Import Certificate data.20
ACE is an automated and electronic
system for processing commercial trade
data. It is the primary system through
which the global trade community files
information about imports and exports
so that admissibility into the United
States may be determined by
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18 See
sections 10104(b)(3) and 10104(c) of the
Agriculture Improvement Act of 2018, Public Law
115–334. Available at: https://www.congress.gov/
115/plaws/publ334/PLAW-115publ334.pdf.
19 See section 10104(c) of the Agriculture
Improvement Act of 2018, Public Law 115–334.
Available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf.
20 See sections 10104(h) and (j) of the Agriculture
Improvement Act of 2018, Public Law115–334.
Available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf.
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government agencies (including AMS)
to ensure compliance.
The data to be entered into ACE
include fields for the information
needed to meet the requirements of an
NOP Import Certificate as defined in the
OFPA: origin; destination; the certifying
agent issuing the NOP Import
Certificate; harmonized tariff code,
when applicable; total weight; and the
organic standard the product was
certified to (7 U.S.C. 6502(13)). For the
purposes of uploading and tracking
NOP Import Certificates, the data must
be available as an electronic format to
meet the requirements of the OFPA (7
U.S.C. 6514(d)(1)).
Both the OFPA and the USDA organic
regulations require certified operations
to maintain and make available to the
Secretary records that concern the
production, harvesting, and handling of
agricultural products that are or that are
intended to be sold, labeled, or
represented as organic. This includes
sufficient records to provide an audit
trail to determine the source, type and
quantity, transfer of ownership, and
transportation of any agricultural
product labeled as organic. Likewise,
both the OFPA and the USDA organic
regulations require certifying agents to
maintain and make available to the
Secretary records concerning its
activities.
This policy also aligns with
international guidelines and norms
related to organic oversight. NOP
considered international standards
established by the Codex Alimentarius
Commission (Codex) 21 and norms
published by the International
Federation of Organic Agriculture
Movements (IFOAM).22 Both provide
for and support the use of transaction
shipment certificates such as the NOP
Import Certificate.
Change From Current Policy
NOP Import Certificates are currently
only used for organic products imported
from countries with which AMS has an
equivalence determination. The USDA
has established equivalence
determinations with Canada, the
European Union, Switzerland, Japan,
21 Section 7 of the Codex Guidelines for the
Production, Processing, Labelling and Marketing of
Organically Produced Foods recommends imported
organic products to be marketed only where the
competent authority or designated body in the
exporting country has issued a certificate of
inspection stating that the lot designated in the
certificate was obtained within an organic system
of production, preparation, marketing, and
inspection.
22 IFOAM Norms define a transaction certificate
as a ‘‘document issued by a certification body or by
the operator, declaring that a specified lot or
consignment of goods is certified.’’
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South Korea, Taiwan, and the United
Kingdom. Organic imports from Canada
are accompanied by an organic
certificate that includes an attestation
statement that the products comply with
the terms of the United States-Canada
Organic Equivalency Arrangement.
Organic imports from the European
Union, Switzerland, Japan, South Korea,
Taiwan, and the United Kingdom are
accompanied by an NOP Import
Certificate. The certifying agent of the
exporter evaluates the request for an
NOP Import Certificate, and upon
verification of the organic shipment,
completes and issues an NOP Import
Certificate. Form NOP 2110–1 is
currently used for this purpose.
In the past, AMS has not required
NOP Import Certificates for organic
exports from countries with which the
United States does not have an organic
equivalence determination. The
rulemaking changes this to make the use
of NOP Import Certificates mandatory,
regardless of an imported product’s
country of origin or if that country has
an equivalency determination with
USDA. Specifically, this rulemaking
requires that all imported products
intended to be sold, represented,
labeled, or marketed as organic in the
United States must be declared as
organic to U.S. Customs and Border
Protection (CBP), using an NOP Import
Certificate.
Alignment of Policy With U.S. Customs
and Border Protection Policies and
Systems
The OFPA, as amended by the 2018
Farm Bill, requires the establishment of
an Organic Agricultural Product Imports
Interagency Working Group, consisting
of members of both the USDA and CBP
(see 7 U.S.C. 6521a).23 The mandatory
use of NOP Import Certificates supports
the working group’s goal to ensure the
compliance of organic agricultural
products imported into the United
States.
Under this policy, AMS and CBP will
collaborate to verify that imported
organic products are associated with
NOP Import Certificates. In April 2020,
the electronic version of the NOP Import
Certificate was deployed in ACE as an
optional filing step for organic imports.
The use of the electronic NOP Import
Certificate will be mandatory once this
rule is fully implemented.
NOP Import Certificates will be
required for any commodity imported
into the United States that is being
23 See section 10104(i) of the Agriculture
Improvement Act of 2018, Public Law No: 115–334.
Available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf.
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Where does the data for the NOP Import
Certificate come from?
The data for the NOP Import
Certificate is generated in the Organic
Integrity Database by the certifying
agent of the exporter. The exporter is
responsible for facilitating the trading,
selling, consigning, shipping, or
exporting of organic product from a
foreign country to the United States. An
organic exporter must be certified
organic by certifying agents accredited
by the USDA or certifying agents
authorized by a trade arrangement or
agreement. Organic exporters may be
the final physical handler of organic
products within a foreign country, or
they may be the entities that facilitate,
sell, or arrange the sale of organic
products shipped to the United States.
This exporter is responsible for
verifying that the organic product
complies with organic standards. This
includes, but is not limited to, verifying
that the import has not been exposed to
a prohibited substance, treated with a
prohibited substance as a result of
fumigation or treated with ionizing
radiation at any point in the products’
movements across country borders.
Organic Integrity Database to generate
the NOP Import Certificate. The request
for an NOP Import Certificate must
include all information required by the
organic exporter’s certifying agent to
complete the NOP Import Certificate.
The certifying agent is required to
confirm the authenticity of the organic
products covered by the NOP Import
Certificate using control systems it
designs for this purpose. The certifying
agent must have and implement a
documented organic control system for
intaking and approving or rejecting the
validity of an NOP Import Certificate
request.
The certifying agent is responsible for
ensuring that the issued NOP Import
Certificate is only associated with an
amount of product that has been
verified to be certified organic. The
certifying agent has the authority to
determine whether it will issue an NOP
Import Certificate for a specific
shipment, or for a specific timeframe
(e.g., weekly, monthly, season) and
amount or volume ceiling. This
determination is to be based on the
capacity and control systems of both the
certifying agent and the certified
operation. There is no limit on the
length of timeframe a certifying agent
chooses. However, the certifying agent
must choose a timeframe that is
appropriate to their administrative
capacity and documented control
system and allows them to verify the
integrity of the specific type and volume
of import.
Once the certifying agent verifies the
authenticity of the organic export, the
certifying agent enters or uploads the
information needed into the Organic
Integrity Database. Each NOP Import
Certificate must be associated with a
certified organic operation listed in the
database, identified by a 10-digit code.
The Organic Integrity Database will
generate a unique NOP Import
Certificate that includes both the 10digit identifier for the operation and a
unique numerical identifier for the NOP
Import Certificate. The certifying agent
will provide the NOP Import Certificate,
or data set with the NOP Import
Certificate number, back to the certified
organic exporter requesting the NOP
Import Certificate. The certifying agent
can cancel or void a NOP Import
Certificate in the Organic Integrity
Database at any time.
How does the certifying agent evaluate
the request for an NOP Import
Certificate?
The certifying agent determines the
format of the NOP Import Certificate
request from the certified operation,
based on the data required for the
Transmitting the NOP Import Certificate
From Exporter to Importer
The certified organic exporter
provides the NOP Import Certificate to
the U.S. importer, who provides it to the
specific entity responsible for entering
import information into the ACE
manifested, sold, marketed, or labeled
organic. NOP Import Certificates are
required for organic commodities
regardless of value or size and is not
applicable for any di Minimis
exemptions under current CBP
regulations.
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Generating the NOP Import Certificate
This section describes how the NOP
Import Certificate data are generated.
NOP Import Certificates must be
generated using the USDA’s Organic
Integrity Database. By the time the rule
is fully implemented, both USDAaccredited certifying agents and organic
certifying agents accredited by countries
with which USDA holds an organic
trade arrangement or agreement
(equivalence determination or
recognition arrangement) will have
access to the Organic Integrity Database
to generate NOP Import Certificates.
Only the Organic Integrity Database can
be used to generate valid NOP Import
Certificates, and only accredited organic
certifying agents (USDA or under an
organic trade arrangement or agreement)
are authorized to use the Organic
Integrity Database.
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3565
system. This is typically an importer or
designated Customs broker. The NOP
Import Certificate data can be sent either
electronically or via paper. The U.S.
importer or Customs broker enters the
NOP Import Certificate data into ACE as
part of its standard import filing
process; this process is governed by
timelines determined by CBP. Organic
certifying agents will not have access to
ACE; this activity is done by the
importer or its Customs broker, using
the NOP Import Certificate data
provided by the certifying agent to the
exporter.
As the certified organic product itself
moves from the exporting country into
the United States, all entry
documentation including, but not
limited to bills of lading, bills of sale,
commercial invoices, and packing lists
must clearly state that the product is
organic. Exporting and importing
operations must maintain records
required under § 205.103. CBP may hold
shipments at the border to address
health and safety issues or violations of
U.S. trade laws with a specific
commodity or shipment.
Importer Responsibilities
Upon receiving a shipment, an
organic importer must verify that the
organic product(s) comply with the
USDA organic regulations. This
includes ensuring that an NOP Import
Certificate is associated with the
product received. It also includes
verifying that the import has not been
treated with a prohibited substance as a
result of fumigation or treated with
ionizing radiation at any point in the
products’ movements across borders.
Verification may take many forms,
depending on the documentation
provided, and country and commodity.
The importer must have an organic
control system that documents how this
verification is conducted to protect the
organic integrity of imported product.
This control system is reviewed by the
importer’s certifying agent.
Both the organic exporter and U.S.
organic importer must maintain records
of NOP Import Certificates, and these
records must be available for inspection
by the NOP and certifying agents in
accordance with § 205.103. Certifying
agents that are overseeing imports of
organic products into the United States
must have a system for ensuring that
operations receiving organic product are
receiving and maintaining NOP Import
Certificates, and that they are not
accepting more product from any
providers than is authorized by NOP
Import Certificates.
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Connecting NOP Import Certificate With
ACE Import Data
Once NOP Import Certificate Data is
entered into ACE, the data are
transmitted to AMS for analysis,
surveillance, and enforcement. AMS
will align and validate the data
generated in ACE with the original NOP
Import Certificate entered into the
Organic Integrity Database. This will
connect the data about the actual
imported product back to the data about
the corresponding authorized export,
aligning both sides of the transaction.
This alignment will allow for the
identification of any anomalies or
indicators of fraud, such as: NOP Import
Certificates in ACE that were not
authorized (do not have a valid
certificate number) by a certifying agent
in the Organic Integrity Database (e.g.,
fraudulent certificates); volumes of
product entered in ACE that exceed
those authorized in the Organic Integrity
Database; and/or entries into ACE that
are associated with an operation that is
no longer certified. This type of
automated data-driven surveillance is a
common approach in trade oversight.
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Timing of the NOP Import Certificate
The timing of the NOP Import
Certificate data entry into ACE must
comply with current CBP import filing
requirements for Partner Government
Agencies. The certified organic exporter
must time the NOP Import Certificate
request in such a way that the certifying
agent has time to consider the request
and generate the NOP Import Certificate,
and the exporter has time to deliver it
to the importer or Customs broker before
the CBP filing requirements for the
product.
Requiring an NOP Import Certificate
provides trackable and auditable
verification that organic products
comply with the USDA organic
regulations. This requirement will also
support investigations if noncompliant
products are exported and
misrepresented as organic for sale in the
United States. Given that the Organic
Integrity Database will be the definitive
tool for generating NOP Import
Certificates, additional guidelines on
data entry to generate NOP Import
Certificates will be provided through
that system.
Summary of Changes to the Final Rule
AMS made several changes to the
regulatory text of the SOE proposed rule
when writing this final rule. Changes to
the final rule are discussed below and
are followed by responses to specific
themes from public comment.
• AMS removed ‘‘owner’’ from the
definition of organic exporter, added
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‘‘certified’’ before ‘‘exporter,’’ and ‘‘to
the United States’’ after ‘‘from a foreign
country.’’ This clarifies that the organic
exporter must be certified, and that the
organic exporter may be the final
physical handler of organic products
within a foreign country, or they may be
the entities that facilitate, sell, or
arrange the sale of organic products
shipped to the United States. This was
done to clarify questions about ‘‘who
needs to be certified’’ received during
public comment.
• AMS removed ‘‘of record’’ from the
definition of organic importer and
added a statement that the organic
importer is responsible for entering NOP
Import Certificate data into ACE. This
addresses public commenters’ request to
clarify the role of the organic importer
and the person responsible for entering
data into ACE.
• AMS removed ‘‘through a U.S. Port
of Entry,’’ as all imports must enter
through such a Port, so the phrase is not
needed.
• AMS removed references to ‘‘or
equivalent data source’’ and ‘‘NOP Form
2110–1’’ throughout § 205.273 and
clarified that the Organic Integrity
Database must be used to issue NOP
Import Certificates. AMS has
determined that the Organic Integrity
Database will be the only data source for
NOP Import Certificates because it is a
preexisting, proven tool that meets U.S.
government security requirements, and
already accepts data in multiple
different forms to accommodate data
inputs from other systems. The Organic
Integrity Database is already used and
understood by certifying agents,
including many accredited by both the
USDA and trade partner countries. It is
a system that accepts data in multiple
forms, that any government can engage
with, and that minimizes onboarding
time and learning curve. Using the
Organic Integrity Database as a single
source of certification and import data,
while allowing multiple data upload
methods, will provide secure access to
import data that facilitates the use of
NOP Import Certificates.
• AMS clarified that certifying agents
may issue NOP Import Certificates for a
specific timeframe, if appropriate, not
limited to a single transaction. This
addresses public commenters’ concerns
about generating NOP Import
Certificates for multiple shipments in
short timeframes (e.g., multiple
shipments of fresh produce across the
border). This change allows certifying
agents to determine whether they will
issue an NOP Import Certificate for a
specific shipment or for a specific
timeframe (e.g., weekly, monthly,
seasonally) and amount or volume
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ceiling. Because certifiers conduct
certification activities on a one-year
cycle, it is expected that import
certificates are unlikely to exceed one
year in duration. The certifying agent
must choose a timeframe that is
appropriate to their administrative
capacity and documented control
system, and allows them to verify the
integrity of the specific type and volume
of import.
• AMS clarified the requirement that
certifying agents must have and
implement a documented organic
control system for intaking and
approving or rejecting NOP Import
Certificates. This ensures that certifying
agents have auditable processes and
procedures that NOP can audit to assess
certifying agents’ ability to generate and
approve NOP Import Certificates.
• AMS removed the requirement that
certifying agents must issue NOP Import
Certificates within 30 days. This avoids
any timing discrepancy between NOP
Import Certificate data entry and CBP
import filing requirements. AMS does
not have authority to change CBP entry
requirements. The timing of the NOP
Import Certificate data entry into ACE
must comply with current CBP import
filing requirements for Partner
Government Agencies.
• AMS clarified that organic
importers must have a documented
organic control system to verify NOP
Import Certificates and verify no contact
with prohibited substances or exposure
to ionizing radiation. This is necessary
to ensure that organic importers have
auditable processes and procedures that
certifying agents can review to assess
importers’ ability to verify NOP Import
Certificates and verify the integrity of
imported organic products.
• AMS clarified that organic
importers must verify that the NOP
Import Certificate data accurately
reflects the shipment, which may
include verification of quantities and
types of product specified on the NOP
Import Certificate. This requirement
more clearly states the organic
importer’s responsibility in assessing
and ensuring the integrity of imported
products, providing an additional layer
of oversight at a critical juncture in
organic supply chains.
Summary of Public Comment
The majority of public comments
were strongly in support of AMS’s
proposed mandatory use of NOP Import
Certificates. Many comments discussed
or recommended changes to the NOP
Import Certificate process, including the
timing of NOP Import Certificates, ACE
data entry, how the certificate should
travel with the import, certifying agent
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role and capacity, and how the NOP
Import Certificate would function
within organic trade arrangements and
agreements.
Comments frequently asked AMS to
clarify if NOP Import Certificates can be
issued before or after shipment. They
also noted that the proposed 30-day
requirement to issue NOP Import
Certificates does not align with the 10day ACE entry deadline noted in the
preamble. Some comments requested
that AMS allow up to 30 days to enter
NOP Import Certificate data into ACE,
while others recommended 10 days or
less to help reduce fraud.
Many comments asked AMS to clarify
if an NOP Import Certificate must
‘‘accompany’’ an import or be
‘‘associated with’’ an import. Several
comments requested that AMS require
imports be ‘‘accompanied’’ by an NOP
Import Certificate and that the
certificate travel with the import and be
presented at entry into the United
States, claiming that this would help
prevent fraudulent organic products
from entering the U.S. market. Others
stated a preference to allow NOP Import
Certificates to ‘‘be associated’’ with
shipments, noting that this flexibility is
needed to match the frequency and pace
of land imports via truck and rail.
Several comments noted that issuing
NOP Import Certificates for individual
shipments would be difficult for highvolume, high-frequency imports,
especially those from Canada and
Mexico. These comments asked AMS to
consider allowing certifying agents to
issue NOP Import Certificates that cover
a specific time period (e.g., quarterly),
product type, and volume. Comments
argued this would reduce administrative
burden and cost to both certified
operations and certifying agents. A few
comments also claimed that some
certifying agents may not have the
administrative capacity or technical
expertise to issue and verify NOP
Import Certificates as proposed.
A few comments asked AMS to clarify
the definitions and roles of exporters
and importers, noting that it is not clear
who is responsible for requesting NOP
Import Certificates, verifying them upon
import, and entering data into ACE.
Some comments also asked AMS to
further define ‘‘equivalent data.’’
Finally, some comments requested
clarification about the general
applicability and use of NOP Import
Certificates, including their use for very
small or infrequent shipments, use by
exporters in a country AMS has a trade
arrangement or agreement with, use of
electronic vs. paper certificates, and use
in trade between two foreign countries.
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Responses to Public Comment
Associated vs. Accompanying
Timing of NOP Import Certificates
(Comment) Several commenters noted
that proposed § 205.273(d) states that
the organic importer of record must
ensure that the shipment is
accompanied by a verified NOP Import
Certificate. This conflicts with the
preamble which states that shipments of
organic product must be associated with
a valid NOP Import Certificate.
(Response) To clarify the requirement,
AMS has removed the term
accompanied from the rule. The NOP
Import Certificate must be associated
with a shipment. This revision
accurately describes AMS’s intent that
organic shipments are associated with,
and not accompanied by, a valid NOP
Import Certificate at the time of entry
into the United States.
(Comment) Commenters requested
that the term associated, located in the
preamble text, be changed to
accompany and that AMS require NOP
Import Certificates to be available upon
entry to the United States, to prevent
fraud in the organic market.
(Response) USDA is requiring that all
organic exports to the United States be
associated with a valid NOP Import
Certificate. By requiring organic imports
to be associated with, and not
accompanied by, an NOP Import
Certificate, USDA will have access to
the import data without restricting or
slowing import and trade of organic
products.
(Comment) AMS received many
comments concerning the 30-day time
frame for certifying agents to review and
issue NOP Import Certificates.
Commenters stated that the 30-day
timeframe will negatively impact
imports of perishable organic product
from Canada and Mexico that require a
rapid import process.
Other commenters stated that the 30calendar-day timeframe for certifying
agents to review and issue NOP Import
Certificates does not align with the
existing 10-day requirement to upload
the NOP Import Certificate data into the
ACE system. Others requested that the
10-day requirement for organic
exporters to enter data from an NOP
Import Certificates or equivalent into
ACE align with the proposed 30-day
requirement for certifying agents to
issue an NOP Import Certificate or
equivalent. Commenters also requested
that the 10-day timeframe to enter NOP
Import Certificate data be reduced to
prevent organic fraud.
More broadly, AMS received
comments asking if NOP Import
Certificates can be issued both before
and after shipment. Additionally,
commenters asked If NOP Import
Certificates could be issued after the
shipment of organic product has already
entered the United States.
(Response) The timing of the NOP
Import Certificate data entry into ACE
must comply with current CBP import
filing requirements for Partner
Government Agencies. AMS does not
have authority to change CBP entry
requirements.
The certified organic exporter must
time the NOP Import Certificate request
in such a way that the certifying agent
has time to consider the request and
generate the NOP Import Certificate, and
the exporter has time to deliver it to the
importer or Customs broker before the
CBP filing requirements for the product.
To address the problem of generating
NOP Import Certificates for multiple
shipments in short timeframes (e.g.,
multiple shipments of fresh produce
across the border), AMS is granting the
certifying agent the authority to
determine whether it will issue an NOP
Import Certificate for a specific
shipment, or for a specific timeframe
(e.g., weekly, monthly, season) and
amount or volume ceiling. The
certifying agent is responsible for
ensuring that the issued NOP Import
Certificate is only associated with an
amount of product that has been
verified to be certified organic.
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Certifying Agent Capacity
(Comment) AMS received several
comments highlighting that organic
certifying agents lack the capacity to
issue the number of NOP Import
Certificates that would be required
under the proposed rule at one per
shipment. Comments specifically
referenced the high-volume of organic
products coming by truck and rail from
Mexico and Canada.
(Response) It is the certifying agent’s
responsibility to ensure that the
exporting operation has the capacity to
produce or handle the product covered
by the NOP Import Certificate. When a
certifying agent issues a NOP Import
Certificate, it is validating that the
product is truly organic; therefore, it
must have adequate control systems to
verify these claims.
To address the problem of generating
NOP Import Certificates for multiple
shipments in short timeframes (e.g.,
multiple shipments of fresh produce
across the border), AMS is granting the
certifying agent the authority to
determine whether it will issue an NOP
Import Certificate for a specific
shipment, or for a specific timeframe
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(e.g., weekly, monthly, season) and
amount or volume ceiling. The
certifying agent is responsible for
ensuring that the issued NOP Import
Certificate is only associated with an
amount of product that has been
verified to be certified organic.
(Comment) AMS received several
comments that recommended a
staggered implementation timeline for
the NOP Import Certificate requirement
to ensure certifying agents have the
administrative capacity to process
additional NOP Import Certificates.
Several comments also expressed
concern about the increased cost
associated with issuing NOP Import
Certificates. Comments noted that
certifying agents would need to hire and
train additional technical staff to
comply with the proposed requirements
for NOP Import Certificates.
(Response) Under the current USDA
organic regulations, certifying agents are
not allowed to provide certification
services that are outside its
administrative capacity. While a
reasonable implementation period is
being provided to fully update the
Organic Integrity Database to generate
NOP Import Certificates, certifying
agents are not to issue any NOP Import
Certificates without having adequate
expertise and staffing to verify the
organic status of products it oversees
under the organic program.
(Comment) Commenters asked how
certifying agents will verify whether a
shipment is compliant with the USDA
organic regulations based on an NOP
Import Certificate.
(Response) Certifying agents that are
overseeing exports of organic products
to the United States must have and
implement a documented organic
control system for intaking and then
approving or rejecting an NOP Import
Certificate request. The certifying agent
is responsible for ensuring that the
issued NOP Import Certificate is only
associated with an amount of product
that has been verified to be certified
organic. Certifying agents that are
overseeing importers of organic
products into the United States must
have a system for ensuring that
operations receiving organic product are
receiving and maintaining NOP Import
Certificates, ensuring that importers
have met the requirements of this
section, and that they are not accepting
more product from any providers than
is authorized by NOP Import
Certificates.
General Applicability
(Comment) AMS received comments
asking if NOP Import Certificates would
be required for small, retail, and mixed
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shipments of organic product imported
into the United States.
(Response) NOP import Certificates
will be required for any commodity
imported into the United States that is
being manifested, sold, marketed, or
labeled organic. NOP Import Certificates
are required for organic commodities
regardless of value or size and is not
applicable for any de minimis
exemptions under current CBP
regulations. A very limited number of
exemptions will be allowed for items
such as, but not limited to, food
donations, non-retail samples, and
humanitarian efforts.
(Comment) Commenters asked if NOP
Form 2110–1, NOP Import Certificate, is
mandatory and whether a paper copy
would be permitted. Commenters also
asked if certifying agents would issue
physical or digital copies of NOP–2110–
1 to operations.
(Response) Only the NOP Import
Certificate and its associated data,
generated from the Organic Integrity
Database, is a valid NOP Import
Certificate. Either a paper-based or
electronic NOP Import Certificate may
be used. Certifying agents will
determine the format it will use to
provide the exporter with the NOP
Import Certificate data.
ACE Data Entry
(Comment) We received comments
requesting AMS clarify the definition of
‘‘equivalent data source’’ by providing
additional text in § 205.273(e).
Commenters requested the requirement
explicitly state that USDA is the sole
authority that determines equivalent
data sources.
(Response) In the final rule, we have
removed the term ‘‘equivalent data
source.’’ All NOP Import Certificates
will be generated using the Organic
Integrity Database. AMS provides
multiple ways to upload or enter data
into the Organic Integrity Database. We
have determined it will be the only data
source for NOP Import Certificates
because it is a preexisting, proven tool
that meets U.S. government security
requirements, and a centralized system
is needed to facilitate supply chain
traceability and to assess authorized
import certificate data against actual
import data generated by CBP and
reported back to AMS. The Organic
Integrity Database allows data
submittals in multiple formats, such as
direct data entry, data spreadsheet
uploads, and automated programming
interfaces. A data dictionary is also
public, allowing external parties to
easily map their own systems and data
exports to the tool. The Organic
Integrity Database is already used and
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understood by certifying agents,
including many accredited by both the
USDA and trade partner countries. It is
a system that any government can
engage with that minimizes onboarding
time and learning curve. Using the
Organic Integrity Database as a single
source of certification and import data,
while allowing multiple data upload
methods, will provide secure access to
import data that facilitates the use of
NOP Import Certificates.
(Comment) We received a number of
comments about the respective roles of
the exporter and importer with respect
to the NOP Import Certificate. Several
comments stated that the organic
exporter does not have access to the
CBP ACE system and is not the party
that would enter the required data into
ACE. Commenters recommended that
the importer of record be the entity
responsible for entering data into ACE.
Comments stated that the proposed
definition of organic importer of record
is unclear and does not reliably identify
the party capable of ensuring each
shipment is associated with an NOP
Import Certificate.
(Response) NOP Import Certificates
must be generated by the certified
organic exporter’s certifying agent, using
the USDA’s Organic Integrity Database.
Only the Organic Integrity Database can
be used to generate valid NOP Import
Certificates, and only accredited organic
certifying agents (USDA or under an
organic trade arrangement or agreement)
are authorized to use the Organic
Integrity Database.
Once the NOP Import Certificate is
generated in the Organic Integrity
Database, the exporter’s certifying agent
provides the NOP Import Certificate, or
data set with the NOP Import Certificate
number, back to the certified organic
exporter who requested the NOP Import
Certificate. The certified organic
exporter then provides the NOP Import
Certificate to the U.S. importer or buyer,
who provides it to the specific entity
responsible for entering import
information into the ACE system. This
is typically an importer or designated
Customs broker. That importer or
Customs broker enters the NOP Import
Certificate data into the ACE system as
part of its standard import filing
processes, including the Entry Summary
Process. Organic certifying agents will
not have access to ACE; this activity is
done by the importer or its Customs
broker, using the NOP Import Certificate
data provided by the certifying agent to
the exporter.
(Comment) Commenters asked how
imported organic product would be
identified in ACE without an organic
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Harmonized Tariff Schedule (HTS)
code.
(Response) The NOP Import
Certificate in ACE has been programmed
to enable NOP Import Certificate entry
for a wide range of products, including
agricultural products and textiles, not
just those with an organic HTS code. An
organic HTS code is not required to
upload NOP Import Certificate data into
ACE.
Trade Arrangements and Agreements
(Comment) AMS received comments
requesting that foreign-based certifying
agents operating under recognition
arrangements be required to list organic
operations in the Organic Integrity
Database. As noted by commenters, the
absence of that data makes it difficult
for organizations to verify the
certification status of foreign-certified
operations.
(Response) AMS is changing access to
the Organic Integrity Database to
include organic certifying agents and
operations operating under organic
trade arrangements or agreements, such
as equivalency and recognition
arrangements. Certified organic
operations covered under trade
arrangements or agreements will need to
be listed in the Organic Integrity
Database by their certifying agents for
the certifying agents to be able to
generate NOP Import Certificate for
valid products entering the United
States as organic.
(Comment) We received comments
asking how NOP Import Certificates
would apply to trade of organic
products under, and outside of, an
equivalency arrangement. Additionally,
commenters requested more information
about how NOP Import Certificates
would apply to NOP-certified products
traded between foreign countries.
(Response) The NOP Organic Import
Certificate is required for any product
Section
205.307 ...............................
C. Labeling of Nonretail Containers
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Labeling of nonretail containers.
Paragraphs (a) through (c).
Background
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imported into the United States that is
being manifested, sold, marketed, or
labeled organic, regardless of the
product’s country of origin or if that
country has an equivalency
determination with USDA. Organic
products imported from any country
with which AMS has an equivalency
determination must follow the same
NOP Import Certificate requirements
outlined in this rule. Other countries
may also have their own unique filing
requirements for organic products
coming into their countries; organic
businesses need to consult with their
supply chains to determine those
requirements.
Final regulatory text
Accurate labeling of non-retail
containers used to ship or store organic
products is critical to organic integrity.
Proper labeling reduces
misidentification and mishandling,
facilitates traceability and product
verification, reduces the potential for
organic fraud, and allows accurate
identification of organic product by
customs officials and transportation
agents.
Therefore, this rulemaking requires
that all nonretail container labels must
identify contents as organic and include
information linking the container to
audit trail documentation. Additionally,
audit trail documentation associated
with a nonretail container must identify
the last certified operation that handled
the product. Affected entities may
include but are not limited to: certified
and noncertified operations that store
and transport organic product in
nonretail containers; certifying agents;
and inspectors.
The organic regulations previously
only required a production lot number
on nonretail containers labels used to
ship or store organic product. Other
information—such as identification of
the product as organic, and special
handling instructions—were optional,
but not required on nonretail container
labels. Based on the NOP’s experience
enforcing the organic regulations, this
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lack of information created gaps in the
organic chain of custody, complicated
the verification of organic integrity, and
increased the likelihood of organic
fraud.
To reduce the prevalence of organic
fraud and increase oversight of organic
supply chains, nonretail containers are
now required to be marked with a
statement identifying the product as
organic and must include unique
information that will link the nonretail
containers to audit trail documentation.
Unique identifying information could
include lot numbers, shipping
information, or a unique identifier for
that shipment. Accurate labeling will
identify contents as organic as a
container moves through the supply
chain; this will reduce mishandling and
help maintain an audit trail and
improve traceability.
Nonretail Containers: Description and
Use
Nonretail containers are defined
under § 205.2 of the USDA organic
regulations as ‘‘any container used for
shipping or storage of an agricultural
product that is not used in the retail
display or sale of the product.’’
Nonretail containers are used to ship or
store either packaged or unpackaged
organic products, and may include the
following:
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• Produce boxes, totes, bulk
containers, bulk bags, flexible bulk
containers, harvest crates and bins;
• Boxes, crates, cartons, and master
cases of wholesale packaged products;
and
• Trailers, tanks, railcars, shipping
containers, vessels, cargo holds,
freighters, barges, grain elevators, silos,
grain bins, or other methods of bulk
transport or storage.
Nonretail containers are not used to
display organic products for sale to the
consumer at retail establishments.
Packages that display organic products
for retail sale to the consumer must be
labeled according to §§ 205.303 and
205.306.
What must be included on nonretail
container labels?
Nonretail containers used to ship or
store organic products must be clearly
labeled with a statement that identifies
the product as organic. Clearly visible
organic identification alerts handlers
that the contents of the nonretail
container may require special care, thus
reducing accidental mishandling of the
product, such as treatment with a
prohibited substance or commingling
with conventional product during
transport and storage. Operations may
use abbreviations or acronyms to
identify products as organic, provided
that they are clear and easily
understood. This provides flexibility for
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operations to meet the requirements of
§ 205.307(a)(1) and makes it easier to
label containers with limited space or
containers that are difficult to label due
to their size, shape, material, or use.
Nonretail containers must also be
clearly labeled with information that
links the container to audit trail
documentation (see § 205.2 for
definition of audit trail). This could be
a production lot number, shipping
identification, or other unique
information that handlers can use to
trace the container to its associated
audit trail documentation. This creates
a clear link between container and audit
trail and minimizes the size of labels by
allowing some information to be listed
in associated documentation, instead of
directly on the nonretail container label.
Operations may use temporary labels
or signage to meet the requirements of
§ 205.307(a). This provides additional
flexibility for containers that may be
difficult to label due to size, shape,
material, or use.
Revisions to § 205.307 do not limit the
information that can be on a nonretail
label. This gives operations the
flexibility to include details they deem
critical to the integrity of specific
products. For example, an operation
may opt to include special handling
instructions, the USDA organic seal for
qualifying products, the operation or
certifying agent name, or contact
information on the nonretail label.
Nonretail Containers and Audit Trail
Documentation
Nonretail containers used to ship or
store organic products must be labeled
with information that links the
container to audit trail documentation
(§ 205.307(a)(2)). Such documentation
must be sufficient to determine the
source, transfer of ownership, and
transportation of the product (see
definition of audit trail in § 205.2) and
must identify the last certified operation
that handled the product (§ 205.307(b)).
Listing the last certified organic
operation provides a point of contact to
verify the organic status of a product
and supports operations’ traceability,
recordkeeping, and fraud prevention
requirements (§§ 205.103(b)(2)–(3) and
205.201(a)(3)). It also supports on-site
inspections and supply chain
traceability audits conducted by
certifying agents (§§ 205.403(d)(5) and
205.501(a)(21)) by ensuring good
recordkeeping of the critical transfers
between certified operations.
Exception to Organic Identification on
Nonretail Containers
Nonretail containers used to ship or
store agricultural products packaged for
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retail sale with organic identification
visible on the retail label are not
required to identify product as organic
per § 205.307(a)(1). Examples include
master cases and pallets where the
organic identification (e.g., the USDA
organic seal) of individual retail units is
visible. These are exempt from
§ 205.307(a)(1) because the organic
identification is visible on the retail
label.
These types of nonretail containers
are only excepted from the requirements
of § 205.307(a)(1). All nonretail
containers must be linked or traceable to
audit trail documentation per
§ 205.307(a)(2); this ensures traceability
of the product in the containers and
supports organic integrity during
transport, storage, and handling.
Summary of Changes to the Final Rule
AMS made several changes to the
regulatory text of the SOE proposed rule
when writing this final rule. Changes to
the proposed rule are discussed below
and are followed by specific themes
from public comment.
• AMS simplified the requirement to
list full organic identification (e.g., ‘‘100
percent organic,’’ or ‘‘made with organic
. . .’’) to ‘‘identification of product as
organic,’’ which provides more
flexibility to operations and shortens the
organic identification statement without
changing the statement’s intent or its
utility as immediate and clear
identification of nonretail containers.
This change was made in response to
public comment.
• AMS revised the requirement to list
production lot numbers or shipping
identification. This information is now
used to link a container to audit trail
documentation. To reduce
administrative burden and cost to
operations, AMS is only requiring the
most critical information on nonretail
container labels: organic identification
and information that links the container
to audit trail documentation. This
maintains traceability and integrity by
requiring nonretail containers to be
linked to audit trail documentation,
which must identify the last certified
operation that handled the product and
must be sufficient to determine the
source, transfer of ownership, and
transportation of the product.
• AMS removed the requirement to
identify the product’s certifying agent
on nonretail labels because this
information may be included in audit
trail documentation linked to nonretail
containers. Removing this requirement
limits information on nonretail labels to
the most critical information, thereby
reducing cost and burden without
sacrificing integrity.
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• AMS added a requirement that
audit trail documentation associated
with a nonretail container must identify
the last certified operation that handled
the product. This allows operations to
verify the source of organic products
they receive and provides a record trail
that certifying agents can use to conduct
full supply chain traceability audits and
verify organic status.
• The final rule no longer requires
organic identification on nonretail
containers of retail-labeled products.
This avoids undue administrative
burden, cost, and redundant
information when organic identification
is already visible on the products’ retail
labels.
• AMS removed the list of optional
information that may be listed on
nonretail container labels. This list is
not necessary because operations may
optionally include any additional
information on nonretail labels if they
wish.
Summary of Public Comment
Public comments strongly supported
mandatory organic identification on
nonretail container labels. However,
many comments requested the
flexibility to use alternatives like
abbreviations and common names.
Commenters stated that the proposed
rule’s requirement to use specific (and
sometimes lengthy) statements would
add cost and be difficult to apply to
containers with limited space.
Commenters also requested that AMS
require generic product names—e.g.,
‘‘organic tomatoes’’—on labels, claiming
that this information is needed to
quickly identify the contents of
nonretail containers.
Other commenters requested AMS
mandate additional information on large
nonretail container labels to include
country of origin, special handling
instructions, and the USDA organic seal.
Additionally, comments pointed out
that nonretail labels should not be
limited to the information explicitly
listed in § 205.307, and requested that
NOP allow operations to include other
types of information on labels.
Responses to Public Comment
(Comment) We received comments
requesting AMS require all nonretail
containers display the information
described in § 205.307, regardless of size
or type (i.e., not allow exceptions for
large nonretail containers used for
transport or storage). Additionally,
commenters noted that there was no
definition or description outlining what
type of containers would be exempt
from the labeling requirements.
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(Response) All nonretail containers of
organic products must be labeled with
information that links the container to
audit trail documentation, regardless of
size, shape, or use. This ensures
information needed to verify and trace
the product is available to those
handling the product. Only nonretail
containers used to ship or store
agricultural products packaged for retail
sale with organic identification visible
on the retail label are excepted from the
requirements of § 205.307(a)(1).
(Comment) Commenters requested the
name and contact information of the
certified operation be a mandatory field
on all nonretail container labels because
a certifying agent name alone is not
sufficient to match a physical product to
an organic certificate. Other commenters
also requested that the operation’s
address or the NOP operation ID also be
included.
(Response) AMS is only requiring the
most critical information on nonretail
container labels: organic identification
and information that links the container
to audit trail documentation. This
reduces administrative burden and cost
to operations. Traceability and integrity
are maintained by requiring nonretail
containers be linked to audit trail
documentation, which must identify the
last certified operation that handled the
product. Audit trail documentation
must be sufficient to determine the
source, transfer of ownership, and
transportation of the product (see audit
trail in § 205.2).
(Comment) We received comments
requesting that listing the certifying
agent be optional because it was
redundant for master cases of retailpackaged product and added to the cost
of the label.
(Response) AMS does not require
listing the certifying agent on nonretail
container labels. Such information may
be listed in audit trail documentation;
operations may choose to do this to
verify organic status of the product or
determine the source, transfer of
ownership, and transportation of the
product. Section 205.307(c) excepts
nonretail containers of retail-packaged
products from listing organic
identification if the retail packages
clearly identify the product as organic.
(Comment) AMS received comments
noting both disagreement and confusion
regarding which operation/certifying
agent pair is required to be on the
nonretail label. Commenters stated that
the proposed revision (‘‘producer of the
product, or . . . the last handler that
processed the product’’) may not
indicate the appropriate operation for
verification purposes or in private
labeling scenarios.
(Response) Section 205.307(b)
requires that a nonretail container’s
audit trail documentation identify the
last certified operation that handled the
product. The certifying agent that
certified this handler may be listed in
audit trail documentation; operations
may choose to do this to verify organic
status of the product or determine the
Section
205.2 ...................................
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205.403 ...............................
source, transfer of ownership, and
transportation of the product.
(Comment) We received comments
stating that special handling
instructions are critical to the integrity
of organic products in the supply chain
and requested that AMS make this
information mandatory on all labels.
Commenters also inquired about what
special handling instructions should
include.
(Response) We are not requiring
special handling instructions on
nonretail container labels; this reduces
administrative burden and cost to
operations without risking integrity.
Operations may include special
handling instructions (or other
information) on nonretail containers if
they deem it necessary.
(Comment) AMS received comments
requesting the mandatory use of tamperevident seals on nonretail containers.
Commenters argue that tamper-evident
seals may help prevent fraud and
mishandling of organic product.
(Response) AMS is not requiring
tamper-evident seals on nonretail
containers; this avoids potential undue
administrative burden and costs to
operations. Operations may use tamperevident seals on nonretail containers if
they deem it necessary.
D. On-Site Inspections
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definition for Unannounced inspection.
On-site inspections.
Paragraphs (b)(1) and (2) and (d)(4) and (5).
On-site inspections of certified
organic operations are a critically
important tool used to verify an
operation’s compliance with the Act
and the organic regulations. This
rulemaking strengthens the utility of onsite inspections by requiring that
certifying agents:
• Conduct a minimum number of
unannounced inspections each year.
• Conduct mass-balance audits
during on-site inspections.
• Verify traceability of product and
ingredients within an operation during
on-site inspections.
• Verify traceability of product in an
operation’s supply chain back to the last
certified operation during on-site
inspections.
These requirements will strengthen
organic integrity and supply chain
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traceability by requiring the use of
proven best practices during inspection
of organic production and handling.
Entities affected by this policy may
include certifying agents, certified
operations, and operations applying for
certification. Organic stakeholders
should carefully examine the regulatory
text and policy discussion below.
Unannounced Inspections—Background
Unannounced inspections are an
effective and useful tool to ensure
compliance across certified operations
and bolster consumer trust in the
organic label. NOP previously issued an
instruction (NOP Instruction 2609) on
unannounced inspections, which
recommends that certifying agents
conduct unannounced inspections of
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five percent of their total certified
operations per year as a tool for
ensuring compliance with the
regulations.24 This NOP instruction was
supported by a recommendation made
by the NOSB in December 2011.25 The
organic regulations previously allowed
for, but did not require, unannounced
inspections, leaving this to the
discretion of the certifying agent.
24 NOP 2609, Instruction, Unannounced
Inspections. September 12, 2012. Available in the
NOP Program Handbook: https://
www.ams.usda.gov/sites/default/files/media/
2609.pdf.
25 NOSB Recommendation, Unannounced
Inspections. December 2, 2011. Available on the
AMS website: https://www.ams.usda.gov/sites/
default/files/media/NOP%20CACC%20
Final%20Rec%20on%20Unannounced%20
Inspections.pdf.
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Therefore, AMS has codified the
requirement for certifying agents to
conduct a minimum number of
unannounced inspections annually of
certified operations.
Use of Unannounced Inspections
To clarify the difference between
unannounced inspections and full
annual inspections, AMS is defining the
term unannounced inspection as ‘‘The
act of examining and evaluating all or a
portion of the production or handling
activities of a certified operation
without advance notice to determine
compliance with the Act and the
regulations in this part.’’ 26 Note that
unannounced inspections are different
from a full annual inspection because
the scope of the inspection may be
limited to a portion of the operation or
the operation’s activities, and certifying
agents must conduct the inspection
without advance notice.
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Scope of Unannounced Inspections
Relative to a full annual on-site
inspection, an unannounced inspection
may be limited in scope, depth, and
breadth and may cover only a portion of
the operation or the operation’s
activities, such as parcels, facilities,
products, or a review of records. This
allows unannounced inspections to be
used as a risk-based tool to address
specific needs, such as investigation of
a complaint or high-risk area. Inspectors
may conduct sampling during an
unannounced inspection. Samples
collected may count towards the
number of samples a certifying agent
must collect annually per § 205.670(d)
of the organic regulations. Sample
collection alone, however, does not
qualify as an unannounced inspection.
When unannounced inspections are
limited in scope, they are not required
to follow the requirements of
§ 205.403(c)(2), (d), or (e). This means
unannounced inspections:
• May be conducted when an
authorized representative of the
operation is not present and the
inspector is not trespassing.
• May be conducted at any time of
year.
• Do not have to verify all areas or
activities of the operation like a full,
annual inspection.
• Do not have to include an exit
interview with an authorized
representative of the operation.
26 Compare to the definition of inspection at 7
CFR 205.2: The act of examining and evaluating the
production or handling operation of an applicant
for certification or certified operation to determine
compliance with the Act and the regulations in this
part.
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An unannounced inspection may
fulfill the requirement for a full annual
on-site inspection, provided that the
inspector meets all requirements for an
annual on-site inspection per § 205.403.
This includes meeting the timing, scope,
exit interview and documentation
requirements for annual inspections.
The exception is that the inspection
would not be scheduled in advance
with the operation’s awareness. If an
unannounced inspection will serve as
the annual inspection, an authorized
representative must be present.
Selecting Operations for Unannounced
Inspections
To maximize the effectiveness of
unannounced inspections, certifying
agents are encouraged to select
operations from a range of different
production and handling types,
products, and locations. Operations may
be selected randomly, by risk, in
response to a complaint or investigation,
or other criteria. The number of
unannounced inspections to be
conducted annually should be
calculated by rounding up to the nearest
whole number, so that certifying agents
with very few certified operations (e.g.,
under 20 operations) are still required to
conduct at least one unannounced
inspection per year.
Planning and Scheduling Unannounced
Inspections
Unannounced inspections should be
conducted without advance notice to
the operation. However, some
unannounced inspections may require
advance notice (e.g., to ensure that
portions of an operation are accessible
or safe to access). Therefore, a certifying
agent may notify an operation up to four
hours prior to the inspector arriving
onsite. As a best practice, certifying
agents are encouraged to disclose their
process for unannounced inspections,
including a policy on inspector access
to certified operations, and to train
inspectors to prevent trespassing or
breaking laws when accessing an
operation. An operation’s refusal to
allow an inspector access to any portion
of the operation is a violation of
§ 205.403 and warrants a notification of
noncompliance.
Following an unannounced
inspection, an inspection report must be
written by the inspector and reviewed
by the certifying agent. The results of
the inspection must be communicated
to the inspected operation per
§ 205.403(f) and the certifying agent’s
internal protocols.
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Certifying Agent Ability To Conduct
Unannounced Inspections
Certifying agents must be able to
conduct unannounced inspections of
any operation they certify. Therefore,
AMS requires that certifying agents only
accept applications for certification or
continue certification from operations
for which the certifying agent is able to
conduct unannounced inspections. To
ensure consistency, transparency, and
accountability, certifying agents are
expected to describe the areas where
they operate in the written materials
they provide to both applicants and
certified operations, and review the
locations of all operations during their
application review or annual review.
A certifying agent that cannot conduct
unannounced inspections in an
applicant’s or certified operation’s
location due to logistical challenges,
staffing, security, or other reasons, is
considered to not have the
administrative capacity for certification
activities in that area, consistent with
§ 205.501(a)(19). In this case, the
certifying agent must document the
specific reasons it does not have the
administrative capacity to certify in that
area, and must inform the applicant or
certified operation to seek certification
from another certifying agent. If new
certification is not obtained, the
operation’s certification would be
suspended/revoked. This process is
similar to the current procedures used
when a certifying agent surrenders its
accreditation or is suspended/revoked.
For additional information about
unannounced inspections, certifying
agents may refer to NOP Instruction
2609.
Mass-Balance and Traceability Audits
During On-Site Inspections
Traceability of organic products is
critical to verification of organic
integrity. Therefore, AMS requires that
certifying agents verify quantities and
traceability of organic products
produced or handled by an operation
through mass-balance and traceability
audits. Audit tools are the premier
methods to verify organic integrity. The
importance of audits has increased
because transaction certificates, which
certifying agents relied upon in the past
to verify the organic status of specific
loads or sales or organic products, are
neither required by the USDA organic
regulations nor universally issued by
certifying agents.
Mass-Balance Audits
During on-site inspections, certifying
agents must verify that the quantities of
organic product and ingredients
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produced or purchased by an operation
accounts for organic products and
ingredients used, stored, sold, or
transported by the operation
(§ 205.403(d)(4)). Commonly known as a
‘‘mass-balance’’ or ‘‘in-out’’ audit, this
verification is an effective method of
detecting and discouraging organic
fraud.
Mass-balances may be performed on
products that are produced on an
operation, but then used or stored onsite and not sold (e.g., silage produced
on-site as feed for dairy animals). Massbalance covers quantities of agricultural
products; other quantitative assessments
such as dry matter intake and stocking
rate verification are not mass-balances.
To conduct these mass-balance audits,
certifying agents may choose a sub-set of
products based on risk or other factors.
With respect to multi-ingredient
products, certifying agents may choose
a single ingredient or multiple
ingredients to mass-balance. When a
single ingredient is selected, a best
practice is to choose an ingredient that
is high-risk or used in several products.
Mass-balances do not replace the
recommended best practice of also
conducting yield analyses at producer
operations. Yield analysis looks at
whether harvested quantities are
consistent with expected yields. This is
an important tool to assess the potential
for commingling of noncertified/
nonorganic products with organic
products.
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Traceability Audits
Successful traceability within organic
supply chains requires three basic
elements: (1) traceability within a single
operation; (2) traceability one step back
from an operation in a supply chain;
and (3) traceability by a third party
along an entire supply chain, source to
consumer.
Therefore, during all annual
inspections certifying agents must verify
the traceability of organic product both
within an operation and verify
traceability back to an operation’s
suppliers (§ 205.403(d)(5)).27 This
means that a certifying agent must verify
that an operation can trace the products
it produces or handles during the full
time the operation possesses those
products, from time of purchase or
acquisition, through production, to sale
or transport. This includes ingredients
or products that the operation handles
but may not own.
27 The third traceability element, traceability
along an entire supply chain, is addressed in 7 CFR
205.501(a)(21), and discussed in this rulemaking in
Section P, Supply Chain Traceability and Organic
Fraud Prevention.
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Additionally, certifying agents must
verify the traceability of products from
an operation’s suppliers
(§ 205.403(d)(5)). Because supply chains
sometimes include operations that are
not certified, certifying agents must
verify compliance of organic products
back to the last USDA-certified organic
operation. Certifying agents may verify
compliance back to the last certified
operation by inspecting and verifying
audit trail documentation and other
records kept by the certified operation
being inspected. This will ensure
oversight of the critical linkages
between certified operations and
support full traceability and verification
of organic products across supply
chains.
Certifying agents must also conduct
supply traceability chain audits when
circumstances meet criteria defined by
the certifying agent (§§ 205.501(a)(21)
and 205.504(b)(7)). These audits would
not be performed at every annual
inspection.
Responses to Public Comment
Virtual/Remote Inspections
(Comment) Several public comments
noted that during the COVID–19
pandemic, virtual inspections, or
sometimes a hybrid of virtual an on-site
inspection, were temporarily used by
certifying agents. Several comments
asked if AMS intends to allow the use
of virtual inspections for operations that
have a demonstrated history of
compliance or are at low risk of organic
fraud.
(Response) Virtual and/or remote
inspections were not included in the
SOE proposed rule and AMS is
therefore not setting specific policy
related to virtual or remote inspections.
The final regulations provide flexibility
so that AMS may consider virtual
inspection policy options in the future.
Unannounced Inspections
(Comment) Several comments asked
AMS to increase the minimum number
of operations that must receive
unannounced inspections beyond the
five percent AMS proposed.
(Response) AMS is finalizing the
proposed requirement that certifying
agents must conduct unannounced
inspections of at least five percent of the
operations they certify. This is
consistent with a 2011 NOSB
recommendation and a current NOP
Instruction document. AMS chose this
percentage because the majority of
USDA-accredited certifying agents
currently complete unannounced
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3573
inspections at this frequency.28 Because
most certifying agents are already
completing unannounced inspections at
this level, this percent should be tenable
for certifying agents, regardless of size.
To justify a higher percentage, AMS
would require additional information,
industry feedback, and data to assess the
potential impact. Comments did not
provide justification or data to support
a higher inspection percentage.
However, certifying agents may choose
to conduct a higher percentage of
unannounced inspections to
supplement their oversight and
enforcement of certified operations.
(Comment) Some public comments
asked if AMS intends to publish criteria
for initiating or using unannounced
inspections.
(Response) AMS is not adding criteria
for using or initiating unannounced
inspections to the regulations.
Unannounced inspections may be
triggered and selected by a variety of
factors, including at random and in
response to complaints or
investigations. The regulations provide
certifying agents flexibility to use
unannounced inspections when and
where they are most effective.
Mass-Balances
(Comment) Several public comments
asked if AMS is requiring one massbalance per certification scope (i.e.,
crops, livestock, handling, wild crops)
of an operation.
(Response) The regulatory text
provides certifying agents the flexibility
to determine where such audits are most
needed within a single inspection.
(Comment) Some comments asked
AMS if mass-balances should be
performed for single-ingredient or
multi-ingredient products, and if massbalances for multi-ingredient products
must balance all ingredients in the
product.
(Response) The final regulatory text
provides certifying agents flexibility to
perform mass-balance audits of both
single- and multi-ingredient products.
For multi-ingredient products, the
certifying agent may choose to massbalance one or more of the ingredients.
E. Certificates of Organic Operation
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
28 42 of the 49 USDA-accredited certifying agents
the NOP audited in calendar years 2018 and 2019
completed unannounced inspections for 5% of the
operations they certify.
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Section
205.2 ...................................
205.404 ...............................
Final regulatory text
Terms defined.
Definition for Organic Integrity Database.
Granting certification.
Paragraphs (b) and (c).
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Certificates of organic operation are
an important tool used by organic
stakeholders to communicate
information about certified operations.
Certifying agents must generate
certificates of organic operation
electronically using the Organic
Integrity Database. Standardized,
electronic certificates maintained in a
publicly accessible database will help to
deter and prevent the use of fraudulent
certificates of organic operation. This
requirement also ensures that
certificates of organic operation have
consistent information and format,
allowing certifying agents and buyers of
organic products to readily validate
certificates of organic operation.
Certifying agents may add their unique
addenda to certificates of organic
operation to provide additional details
about the certified operation.
Affected entities may include
certifying agents, applicants for USDA
accreditation, certified operations and
entities seeking to validate the
certification status of an organic
operation. Readers should carefully
examine the regulatory text and
discussion below to determine if they
are affected by this action.
Background
AMS accredits nearly 80 certifying
agents; only a few currently create
certificates of organic operation using
the Organic Integrity Database. As a
result, more than 70 distinct formats of
certificates of organic operation exist in
the market. This variation increases the
likelihood of alteration and organic
fraud. In addition, AMS consistently
cites noncompliances for certifying
agents who do not include all of the
required information on their
certificates of organic operation. Of the
49 USDA-accredited certifying agents
audited by the NOP in calendar years
2018 and 2019, 16 were cited for issuing
certificates of organic operation not
consistent with USDA organic
regulations and instruction. The use of
a uniform certificate of organic
operation generated through the Organic
Integrity Database eliminates these
inconsistencies and helps avoid
noncompliances.
The requirement for uniform
certificates of organic operation
supports OFPA’s purpose to facilitate
interstate commerce of organic foods (7
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U.S.C. 6501(3)). This rulemaking also
addresses a 2005 NOSB
recommendation to standardize
information on certificates of organic
operation and require certifying agents
to issue and maintain certificates of
organic operation from a common
database.29
Organic Integrity Database and
Certificates of Organic Operation
The certificate of organic operation
communicates information about the
organic certification of an operation.
This rulemaking requires certifying
agents to provide uniform certificates of
organic operation that are electronically
generated from the Organic Integrity
Database.
AMS defines the term Organic
Integrity Database in § 205.2 as the
National Organic Program’s electronic,
web-based reporting tool for the
submission of data, completion of
certificates of organic operation, and
other information, or its successors. The
Organic Integrity Database may also be
referred to as the OID or INTEGRITY.
AMS is responsible for the functionality
of the Organic Integrity Database and
ensuring consistent content and styles
of all certificates of organic operation.
The general public can view
information in the Organic Integrity
Database online at: https://
organic.ams.usda.gov/integrity/
Generating Certificates of Organic
Operation in the Organic Integrity
Database
Section 205.404(b) requires certifying
agents to generate certificates of organic
operation in the Organic Integrity
Database, making it easier for the
certificates to be accessed online by
relevant stakeholders in the organic
supply chain (e.g., other certifying
agents, inspectors). Section
205.501(a)(15) requires certifying agents
to maintain current and accurate data on
operations they certify in the Organic
Integrity Database. Together, sections
205.404(b) and 205.501(a)(15) require
certifying agents to input and maintain
accurate data on the operations they
certify, and to generate certificates of
29 NOSB Recommendation: Information on
Certificates of Organic Operation: https://
www.ams.usda.gov/sites/default/files/media/
NOSB%20Rec%20Standardize%20
Organic%20Certifications%20Certificates.pdf.
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organic operation using the Organic
Integrity Database. This applies to all
USDA-accredited certifying agents
whether foreign- or domestic-based.
Certificates of organic operation
generated in the Organic Integrity
Database include the required
information that stakeholders need to
verify organic status of an operation.
Users can also access the database to see
if an operation’s organic certification
has been suspended, revoked, or
surrendered. In addition to
strengthening organic integrity,
standardized certificate format and data
fields facilitate and simplify verification
of products, ingredients, and suppliers.
The Operation Profile feature in the
Organic Integrity Database also lists the
generic products and services offered by
an operation. The accessibility and
security of this data will reduce
administrative burden on certified
operations that purchase organic
products and ingredients, as well as
certifying agents and inspectors who
monitor compliance.
Certifying agents can continue using
the data submission template and the
web-based form to upload the required
data fields into the Organic Integrity
Database. Additionally, certifying agents
can transfer data from in-house
databases to the Organic Integrity
Database using an Application
Programing Interface (API) to reduce
duplicative data entry. AMS provides a
data submission API guide for certifying
agents on the Organic Integrity
Database’s User Resources page.
Addenda to Certificates of Organic
Operation
Some certifying agents use certificate
addenda to supplement the information
on certificates of organic operation with
more details about an operation and the
products it is certified to produce and/
or handle. Certificate addenda may be
generated and maintained in the
Organic Integrity Database or by
certifying agents’ databases. The
rulemaking allows certifying agents to
continue providing their own
certification addenda to communicate
additional information about an
operation’s certification in a different
format than certificates generated by the
Organic Integrity Database. For example,
an addendum may include information
about an operation’s certification to
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various international organic standards
or the brand names of products that the
operation produces and/or handles that
are not included on the certificate of
organic operation. Certificate addenda
may be issued only for a certified
operation at an approved location(s).
Section 205.404(c) requires five
elements to be on any organic certificate
addenda issued by certifying agents to
deter organic fraud and provide
consistency across certifying agents.
Primarily, the addendum requirements
are intended to ensure that someone
viewing the document is aware that
certification may be verified in the
Organic Integrity Database. The
accuracy of information on addenda,
such as products and labeling
categories, may also be verified in the
Organic Integrity Database (see
Operation Profiles). In summary, an
addendum must identify the name,
location, and contact information of the
operation and certifying agent; an
operation’s unique operation ID from
the Organic Integrity Database;
addendum issue date; a link to the
operation’s certificate or profile in the
Organic Integrity Database; and a
statement citing the Organic Integrity
Database for certificate verification.
Certifying agents may include other data
in addition to the mandatory elements
on certificate addenda.
Summary of Changes to the Final Rule
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AMS revised § 205.2 to replace the
name of the proposed term
‘‘INTEGRITY’’ with ‘‘the Organic
Integrity Database.’’ Additionally, AMS
did not include proposed § 205.404(c)(6)
which would have required expiration
dates on certificate addenda. Many
public comments noted that an addenda
expiration date could cause confusion,
as it could be mistakenly interpreted as
expiration of an operation’s
certification. Organic certification does
not expire; it continues until
surrendered, suspended, or revoked—
see § 205.404(d). Further, several public
comments noted that addenda
expiration dates would increase
workload for certifying agents, as they
would need to update addenda
expiration dates even if there are no
other changes to a certificate of organic
operation. AMS agrees with public
comments and is not finalizing the
requirement for addenda expiration
dates. This will also encourage
stakeholders to adopt the best practice
of verifying certification status in the
Organic Integrity Database, as this tool
will include the most up-to-date
operation and certification information
(see § 205.201(a)(15)).
Summary of Public Comments
Comments generally supported
requirements to including uniform
information on certificates of organic
operation, noting that this would reduce
inconsistencies across the industry on
what information is collected and
maintained. Comments expressed
concern about using the Organic
Integrity Database to generate the
certificate files and some argued that the
proposed changes would instead hinder
the process for certificate generation,
rather than streamlining it. Some
certifying agents noted that they would
be more comfortable and efficient using
their proprietary databases to generate
certificate information and that using
the Organic Integrity Database would be
additional work to enter duplicative
data. Comments requested a method for
certifying agents to easily upload or
transfer their existing data into the
Organic Integrity Database, and to
generate a certificate of organic
operation. In addition, comments
generally opposed including an
expiration date on certificates of organic
operation because a certificate
expiration date could be conflated with
an operation’s certification status.
Responses to Public Comment
(Comment) Comments requested that
NOP change the name of the proposed
term INTEGRITY to Organic Integrity
Database. Commenters stated that
referring to the database’s nickname is
not descriptive enough and could lead
to confusion between the concept of
organic integrity and the database.
(Response) AMS has revised § 205.2
to use the term Organic Integrity
Database to reduce the possibility of
stakeholder confusion by using the full
name of the database.
(Comment) Certifying agents stated
that entering operation data into their
own databases and the Organic Integrity
Database is duplicative work and would
Section
205.406 ...............................
be a financial and administrative burden
because it will require administrative
staff to update both databases.
Commenters also expressed concern
about whether the Organic Integrity
Database would have the functionality
and capacity to withstand the number of
people who would need to access it
regularly, if the Organic Integrity
Database is also used to generate
certificates of organic operation.
(Response) AMS provides tools for
uploading data (data submission
template) and transferring data (via an
API) into the Organic Integrity Database
to reduce duplication. Please see the
data submission API guide for certifying
agents on the Organic Integrity
Database’s User Resources page. In
addition, generating certificates pulls
from the mandatory data that certifying
agents must enter into the Organic
Integrity Database to comply with
§ 205.501(a)(15). Section 205.501(a)(15)
requires certifiers to enter data into the
Organic Integrity Database and states
certifying agents must ‘‘Maintain
current and accurate data in the Organic
Integrity Database for each operation
which it certifies.’’ Certificate
generation does not require additional
data. AMS is prepared for the increased
usage of the Organic Integrity Database
as a result of the rulemaking and will
offer outreach to certifying agents to
support technology integration.
(Comment) AMS received comments
requesting clarification on whether the
rule requires operations to receive
certificates of organic operation
electronically—noting that many
operations prefer (or can only receive)
paper certificates.
(Response) Section 205.404(b) states
that an organic certificate may be
provided to operations electronically—
however, this step occurs after a
certificate has been generated
electronically and does not affect how a
certifying agent transmits certificates to
an operation. Anyone may print a
certificate from the Organic Integrity
Database as needed.
F. Continuation of Certification
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Continuation of certification.
Paragraphs (a) and (b).
AMS has amended § 205.406 to clarify
the annual update requirements for
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organic system plans (OSP) and to
specify that certifying agents are
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required to conduct inspections of
operations they certify at least once per
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calendar year. These changes maintain
requirements for certified operations to
provide certifying agents with updated
and accurate information about their
organic activities while eliminating
duplicative work, and will strengthen
oversight of organic operations through
regular and timely inspection. Affected
entities may include, but are not limited
to certifying agents, certified organic
operations, and operations seeking
organic certification. You should
carefully examine the regulatory text to
determine if you or your organization
may be affected by this action.
Annual Updates of Organic System
Plans
Previously, the organic regulations
required certified operations to submit
an updated OSP in its entirety as part
of annual certification renewal.
Certifying agents implemented this
inconsistently: some required certified
operations submit an entire OSP every
year, while others required operations
only to submit revisions to their OSP.
To clarify OSP requirements, this
rulemaking revises § 205.406(a) to allow
certified organic operations to only
submit sections of its OSP that have
changed to its certifying agent.
Additionally, the rulemaking removes
previous paragraph § 205.406(a)(3),
which required that certified operations
provide, along with its annual update,
an update on the correction of minor
noncompliances previously identified
by the certifying agent as requiring
correction for continued certification.
This requirement was duplicative and
unnecessary, as certifying agents (when
issuing a notice of noncompliance) must
specify a date by which a certified
operation must rebut or correct
noncompliances (§§ 205.662(a)(3) and
205.404(a)). Removal of this
requirement reduces paperwork,
simplifies the certification process, and
ensures that noncompliances are
resolved according to the deadline in
the notice, rather than waiting until the
next certification cycle.
The NOP previously described this
approach in published certifying agent
Instructions (NOP 2615 and NOP
2601).30 This change is necessary to
ensure legal enforceability, consistent
practices between certifying agents, and
reduce the paperwork burden of organic
certification. This will not impact the
requirements for certified operations to
30 NOP 2601 The Organic Certification Process,
December 16, 2013: https://www.ams.usda.gov/
sites/default/files/media/2601.pdf; NOP 2615
Organic System Plans, Organic System Plan
Updates, and Notification of Changes, December 16,
2013: https://www.ams.usda.gov/sites/default/files/
media/2615.pdf.
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maintain an updated OSP or the
requirement for an operation to notify
its certifying agent of operational
changes that may affect its compliance
with organic regulations (§ 205.400(f)).
Further, the on-site inspection of an
organic operation must verify that the
entire OSP is implemented as described.
Frequency and Scheduling for Annual
Inspections
Annual inspection cycles are essential
to vigilant oversight of organic
operations. Inconsistent interpretation
of previous § 205.406 regarding
inspection timing sometimes resulted in
inspection frequencies longer than the
annual timeframe specified in OFPA (7
U.S.C. 6506(a)(5)). For example, former
§ 205.406(b) was sometimes interpreted
to mean that an operation may be
inspected once every 18 months on an
ongoing basis (i.e., two inspections over
a 36-month period compared to three
inspections if conducted annually). To
clarify frequency of on-site inspection,
this rulemaking revises § 205.406(b) to
simplify the regulatory text and clearly
state that inspections are to be
conducted at least once per calendar
year.
Revised paragraph (b) clarifies that all
certified operations must be inspected at
least once in a calendar year, regardless
of (1) when the certified operation was
last inspected and (2) when, or if, the
certified operation provided its annual
updates. This revision allows certifying
agents flexibility to conduct on-site
inspections at any time during the year
(essential for verifying activities
throughout the growing season, for
example) to ensure that an inspection is
conducted every single calendar year.
Additional inspections may be needed
to inspect all portions of an operation to
assess full compliance of an operation
(e.g., during and outside the grazing
season for livestock operations). This
requirement does not replace the need
for additional unannounced
inspections.
Summary of Changes to the Final Rule
AMS did not make any revisions to
the proposed regulatory text. The policy
continues unchanged in this final rule.
Summary of Public Comment
Public comments largely supported
changes made in the proposed rule,
citing support for reduced paperwork,
increased flexibility, and clear
enforceability to uphold organic
integrity. Some comments questioned
the need for the proposed changes,
citing that the work of updating an
entire OSP is not significantly greater
than updating portions of it.
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Several comments supported
revisions to section 205.406(b), which
now requires certifying agents to
conduct on-site inspection once per
calendar year. However, commenters
requested additional flexibility
regarding annual inspections
requirements in the face of extreme
circumstances that may render an inperson inspection unsafe or unfeasible
for the inspector or operation. These
comments cite the COVID–19 pandemic
as an example.
Other comments were generally in
support of the flexibility that the
revisions provide, particularly allowing
inspections to occur when seasonally
appropriate (and potentially reducing
certifying agents’ need to request
additional inspections). However, a few
commenters noted that the calendar
year restriction may cause inspections
to occur one closely after another,
depending on the type of operation and
harvest timeline.
Responses to Public Comment
(Comment) AMS received comments
stating that the revisions to OSP
submission requirements could lead to
inconsistent information across
certifying agent databases and the
Organic Integrity Database.
(Response) All certifying agents are
now required to maintain updated
information on operations they certify
in the Organic Integrity Database. This
requirement will eliminate
inconsistencies.
(Comment) Comments asked if
certifying agents can still request full
updated OSPs from operations they
certify, should the certifying agent deem
the proposed changes significant.
(Response) The rulemaking does not
change or limit the ability of certifying
agents to request information, including
a full OSP, that is needed to determine
an operation’s compliance with the
organic regulations. Paragraph
205.406(a)(4) of the regulations requires
operations to provide certifying agents
information that they deem necessary to
determine compliance with organic
regulations.
(Comment) We received comments
requesting more flexibility regarding
annual inspections (e.g., allowing the
issuance of temporary variances, or
allowing for virtual inspections) in the
face of extreme circumstances that may
render an in-person inspection unsafe or
unfeasible for the inspector or
operation.
(Response) AMS acknowledges that
extreme circumstances may prevent a
certifying agent from completing an onsite inspection once per calendar year.
In such cases, the certifying agent may
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delay inspection, but the delay should
be minimized and explained in the
certifying agent’s inspection report and
records. A certifying agent’s inability to
consistently inspect operations annually
due to access, safety, extreme weather,
or other issues is a failure to carry out
inspection requirements and does not
fulfill the general requirements for
accreditation (§ 205.501(a)(3)). When the
certifying agent is unable to provide
adequate oversight and enforcement, the
certifying agent should not continue to
certify the operation.
(Comment) AMS received comments
proposing an inspection window
anywhere between 7 and 17 months
apart rather than 18 months, thus
allowing inspectors to conduct
inspections when seasonally
appropriate.
(Response) The rulemaking
establishes a minimum frequency for
on-site inspections—at least once per
calendar year—to ensure all certified
operations meet OFPA’s requirement for
annual inspection. If the certifying agent
is unable to complete a full inspection
during a time when land, facilities, and
Section
205.501 ...............................
G. Paperwork Submissions to the
Administrator
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
General requirements for accreditation.
Paragraph (a)(15).
Background
The organic industry, including
certifying agents, certified operations,
consumers, AMS, and other regulatory
agencies use the Organic Integrity
Database to confirm the certification
status of operations, organic status of
products, find contact or product
information for specific operations, and
obtain data points for investigation and
enforcement actions. Timely updates to
maintain data on an operation’s current
status, including certified products and
acreage, is necessary for efficient
business transactions and informed
oversight. The availability of operation
data also reduces the time spent by
certifying agents and by AMS
responding to inquiries about specific
operations because interested parties
can independently access the
information they need.
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activities that demonstrate compliance
can be observed (see § 205.403(c)(2)),
then the certifying agent may conduct
additional on-site inspections, as
allowed in § 205.403(a)(3)(i), to cover
unobserved portions and ensure
compliance with § 205.403.
Final regulatory text
Accurate and current information
about certified operations is critical for
commerce and oversight in the organic
sector. This rulemaking supports
accessible and updated data on organic
operations by requiring certifying agents
to maintain current data on all
operations they certify in the Organic
Integrity Database. Certifying agents and
certified operations may be affected by
these requirements. Readers should
carefully review the regulations and
policy discussion to determine whether
they must comply.
Mandatory Reporting in Organic
Integrity Database
Certifying agents are required to
provide and maintain current
mandatory data on operations in the
Organic Integrity Database. The required
data fields are listed in the INTEGRITY
Data Dictionary and defined in the
Glossary of Terms which can be
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accessed at https://
organic.ams.usda.gov/Integrity/
About.aspx. Some of the data in the
Organic Integrity Database is publicly
accessible. Examples of mandatory,
public data fields include: certification
status, scope(s) of certification (e.g.,
crops, livestock, handling, wild-crop),
and the organic commodities produced
or handled by the operation. This
information is essential for certifying
agents and operations to verify the
organic status of operations and
products and supports efficient business
transactions. Organic acreage is an
example of mandatory data that will not
be publicly available in the Organic
Integrity Database.
Update Frequency
Certifying agents are to establish
processes for updating data in the
Organic Integrity Database in a manner
that keeps information current about
their certified operations. This is needed
to support the industry’s reliance on the
Organic Integrity Database for current
and accurate information about
individual operations. Certifying agents
are required in § 205.662(e)(3) to update
the Organic Integrity Database within 72
hours of an operation’s suspension,
revocation or surrender of certification.
This rule removes the requirement for
certifying agents to provide notices of
denial of certification to the
Administrator following the issuance of
a notice of noncompliance to an
applicant for certification (formerly
§ 205.405(c)). In addition, the rule
removes the requirement for submission
of any notices of denial of certification,
notifications of noncompliance,
notification of noncompliance
correction, notification of proposed
suspension or revocation, or notification
of suspension or revocation (formerly
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§ 205.501(a)(15)(i)). Also, the rule
removes the annual requirement for
certifying agents to submit, by January
2, an annual list of operations certified
during the preceding year (formerly
§ 205.501(a)(15)(ii)). Certifying agents’
adherence to noncompliance procedures
in the regulations are evaluated during
NOP audits, review of appeal cases and
relevant complaints. The requirement
for certifying agents to list operations in
the Organic Integrity Database and their
corresponding certification status makes
the paperwork submission requirements
unnecessary.
Summary of Changes to the Final Rule
AMS renamed the term INTEGRITY
in § 205.501(a)(15) to the Organic
Integrity Database.
Summary of Public Comment
Comments were largely in support of
the proposed revisions, citing that the
changes remove an unnecessary and
redundant step from certifying agents’
day-to-day operations. Commenters also
noted that codifying global use of the
Organic Integrity Database and
maintaining ‘‘accurate and current’’ data
are both critical to ensuring organic
integrity. Commenters noted that the
regulatory text does not explain how
often certifying agents should update
operation data.
Responses to Public Comment
(Comment) Comments requested that
AMS require certifying agents to upload
and maintain data in the Organic
Integrity Database on operations that are
no longer certified, were denied
certification, or withdrew certification
with adverse actions on record.
(Response) The Organic Integrity
Database can identify applicants for
certification that were denied or
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withdrew from certification. AMS
encourages certifying agents to enter
those operations into the Organic
Integrity Database, however, this is not
a required reporting element. The
Organic Integrity Database includes all
operations which are no longer certified
because they are suspended, revoked, or
surrendered.
(Comment) Comments noted that the
rule does not describe the data fields
that certifying agents are required to
complete in the Organic Integrity
Database.
(Response) The Data Dictionary
provides a list of all data fields for the
Organic Integrity Database (https://
organic.ams.usda.gov/Integrity/
About.aspx). The Data Dictionary will
be updated upon implementation of this
rulemaking to make all current fields
mandatory. AMS may add more
mandatory fields in the future based on
industry and NOP needs.
(Comment) Comments requested that
certifying agents be required to update
the Organic Integrity Database within 72
hours of any changes to crops, products,
acreage, or certification status.
(Response) The rule does not require
certifying agents to update all required
data fields within a certain timeframe,
as certifiers need flexibility to create
their own systems for updating and
maintaining current data in the Organic
Integrity Database. However, AMS does
require certifying agents to update
certain data fields within a specified
Section
205.2 ...................................
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205.501 ...............................
timeframe. For example, § 205.662(e)(3)
requires certifying agents to update the
Organic Integrity Database with changes
to an operations certification status
within 3 business days. The Data
Quality Minimum Standards and Best
Practices provides recommendations for
the minimum frequency to update
specific data fields in the Organic
Integrity Database.31
H. Personnel Training and
Qualifications
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definition for Certification review.
General requirements for accreditation.
Paragraphs (a)(4), (5), and (6).
The USDA organic regulations require
that certifying agents use a sufficient
number of trained and qualified
inspectors and certification review
personnel with expertise in organic
production and handling. This
rulemaking enhances existing
requirements with detail about the
qualifications that organic inspectors
and certification reviewers must have in
order to work for certifying agents. By
clarifying the necessary technical skills,
qualifications, and knowledge needed to
conduct organic inspections and
certification review, AMS ensures that
inspectors and certification reviewers
are better prepared to verify organic
compliance, which further strengthens
organic integrity across all levels of the
supply chain and upholds confidence in
the organic label among consumers.
The rule adds new requirements for
certifying agents, inspectors, and
certification personnel:
• Certifying agents must verify that
all inspectors and certification
personnel they contract with or hire
have the minimum required training,
skills, and knowledge.
• Inspectors and certification
personnel must meet a minimum
baseline of knowledge, skills, and
experience before beginning inspection
or certification review activities.
• Inspectors and certification
personnel must meet annual training
requirements to continue inspection or
certification review activities.
• Certifying agents must conduct
periodic observations of inspectors
during inspections (‘‘witness
inspections’’) as a part of their annual
evaluation activities.
• Certifying agents must maintain
policies, procedures, and records
regarding inspector and certification
review personnel training and
evaluation.
The provisions in this chapter affect
current and potential organic inspectors,
certification review personnel, and
certifying agents who employ or
contract with inspectors or certification
review personnel. Some provisions
apply directly to certifying agents’
hiring and evaluation processes. Others
clarify the amount of training inspectors
are required to do to maintain
compliance to the organic regulations.
The following discussion provides
further detail on the provisions and
AMS’s responses to comments received
on the proposed rule.
Background
To continue certification, a certified
organic operation must undergo an onsite inspection at least once a year.
Organic inspectors visit certified organic
operations to thoroughly investigate the
operation’s processes, facilities, and
records. Inspections vary by type and
complexity of operation, but generally
an inspector will review fields to
investigate pest management, soil
fertility management, buffer zones, and
other production techniques; inspect
storage and preparation areas for
evidence of commingling or
contamination with substances
prohibited in organic; review records
and invoices; conduct mass-balance,
traceability, and yield analyses; and
interview a representative of the
operation. The inspector may also
collect samples to test for pesticide
residues. The inspector then prepares an
inspection report that the certifying
agent uses to evaluate the operation’s
compliance with the organic
regulations. In addition to regular, oncea-year scheduled inspections, organic
inspectors also conduct unannounced
inspections, which are conducted
without advance notice and are often
used to target a more limited, but
higher-risk, portion of an operation to
ensure compliance (see the ‘‘On-Site
Inspections’’ portion of this rule for
more detail).
Organic inspectors and review staff
are therefore the most direct form of
enforcement and verification because
they inspect certified organic operations
onsite and report their findings to
certifying agents. Persons performing
certification review activities also
ensure organic integrity by reviewing
these inspection reports along with
organic system plans, inputs, and other
certification documents that are used to
determine compliance with the organic
regulations and grant continued
certification. The role as inspectors and
31 Available in the Organic Integrity Database:
https://organic.ams.usda.gov/integrity/About.aspx.
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reviewers has only grown more critical
as organic operations and supply chains
become more complex and diverse.
Inspection and certification review
are complex professions that require
detailed and highly specialized
knowledge of organic regulation and
agricultural practices and strong
observation, communication, and
investigation skills. Without highly
qualified inspectors and certification
review personnel, loss of organic
integrity—either unintentional or
fraudulent—would go unnoticed and
the organic certification system would
fail. Therefore, these personnel must
adhere to consistent standards of
knowledge, skill, and experience,
relevant to the scope and complexity of
the organic operations they inspect and
review. Consistent standards will ensure
effective oversight and review of organic
operations, catching and preventing
mishandling and fraud at critical points
in the organic supply chain.
The rapidly increased complexity and
scale of the organic market has
multiplied opportunities for
mishandling of organic products and
fraud, especially as supply chains for
organic products increasingly depend
on imported goods. In its February 2018
recommendation, the NOSB referenced
‘‘well-publicized incidents of proven
fraudulent imports in the last year’’ as
a compelling reason to ensure the
industry has ‘‘qualified inspectors
experienced in a broad range of
operations diverse in scope and
scale.’’ 32 For example, a May 2017
Washington Post investigation found
that millions of pounds of imported
corn, soybeans, and ginger had been
fraudulently labeled organic, and
inconsistent inspection practices were
partly to blame.33 Additionally, public
comments from accredited certifying
agents and organic inspector
associations agreed that minimum
training and qualification requirements
for inspectors are necessary to detect
breach of organic integrity and fraud.
AMS recognizes that in a diverse market
where operations can choose their own
certifiers, one critical element of
protecting organic integrity and
preventing fraud is ensuring that all
organic inspectors and reviewers are
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32 NOSB
Formal Recommendation, Inspector
Qualifications and Training, May 29, 2018: https://
www.ams.usda.gov/sites/default/files/media/
CACSInspectorQualificationsRec.pdf.
33 Peter Whoriskey, ‘‘The labels said ‘organic.’ But
these massive imports of corn and soybeans
weren’t.’’ Washington Post. May 12, 2017. https://
www.washingtonpost.com/business/economy/thelabels-said-organic-but-these-massive-imports-ofcorn-and-soybeans-werent/2017/05/12/6d1659842b76-11e7-a616-d7c8a68c1a66_story.html?utm_
term=.97e7f3942427&itid=lk_inline_manual_7.
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held to the same high standards of
training and experience.
The regulations previously lacked
specific detail about qualifications,
experience, and continual training for
inspectors and certification reviewers.
Certifying agents currently set their own
policies and minimum qualifications to
hire inspectors and reviewers, creating
inconsistency in on-site inspection and
certification review. Further, many
inspectors are independent contractors
who are responsible for establishing and
maintaining their own knowledge base.
This diversity of background and
training creates an inconsistent baseline
of knowledge and skill.
In 2012, NOP issued a memo to clarify
that all inspectors and reviewers,
whether staff or independent
contractors, must possess the expertise
and qualifications needed to evaluate
compliance with the USDA organic
standards.34 Additionally, the NOSB
provided recommendations in 2018 to
address the need for specific
qualification and training requirements
for inspectors and persons performing
certification review.35 This rulemaking
codifies the general policy in the 2012
memo and addresses the NOSB
recommendations by describing
baseline qualifications for certifying
agent personnel.
To clarify the portions of this policy
that apply to certification review
personnel, AMS defines the term
certification review as ‘‘the act of
reviewing and evaluating a certified
operation or applicant for certification
and determining compliance or ability
to comply with the USDA organic
regulations.’’ The term does not
encompass performing an inspection,
which is separately defined in § 205.2.36
Examples of certification review
includes reviewing applications for
certification, reviewing certification
documents, evaluating qualifications for
certification, making recommendations
concerning certification, or making
certification decisions and
implementing measures to correct any
deficiencies in certification services.
Establishing baseline qualifications for
the personnel conducting these
activities will lead to greater
34 NOP Memo: Criteria and Qualifications for
Organic Inspectors; April 2012: https://
www.ams.usda.gov/sites/default/files/media/NOPNotice-OrganicInspectorCriteria.pdf.
35 NOSB Formal Recommendation, Inspector
Qualifications and Training, May 29, 2018: https://
www.ams.usda.gov/sites/default/files/media/
CACSInspectorQualificationsRec.pdf.
36 § 205.2 Inspection. The act of examining and
evaluating the production or handling operation of
an applicant for certification or certified operation
to determine compliance with the Act and the
regulations in this part.
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consistency in certification review and
decision.
General Requirements
Section 205.501(a)(4) requires that
certifying agents ‘‘continuously use a
sufficient number of qualified and
adequately trained personnel’’ to
implement and comply with the organic
regulations. Certifying agents must
maintain adequate staffing levels and
the range of expertise needed to perform
the full range of certification activities,
including inspection and certification
review. This includes maintaining an
inspection staff to timely complete
initial on-site inspections, annual
inspections for all operations it certifies,
unannounced inspections on a
minimum of 5 percent of the operations
it certifies annually (see § 205.403(b)),
and any other inspections needed to
ensure compliance with the regulations.
Certifying agents sometimes use
contracted or volunteer personnel (i.e.,
persons not directly employed by the
certifying agent) to inspect operations or
complete certification review.
Therefore, certifying agents must ensure
that all inspectors and certification
review personnel—including staff,
contractors, and volunteers—meet the
requirements of § 205.501(a)(4)–(6). This
means that any person performing
inspection or certification review
activities must meet these requirements,
regardless of their work or contractual
relationship with the certifying agent.
This ensures consistent inspection and
certification review by all certifying
agents.
Knowledge, Skill, and Expertise
Certifying agents must demonstrate
that all personnel they use to conduct
inspection and certification review
continuously maintain knowledge and
skills that qualify them to perform
duties as assigned (§ 205.501(a)(4)(i)(A)
and (a)(4)(ii)(A)). These paragraphs
detail the minimum knowledge and
skills that inspectors and certification
reviewers must have. Because
inspectors and certification reviewers
perform different functions, each must
meet different baseline criteria, although
there is some overlap, such as
knowledge and skill of the organic
regulations, traceability audits, and
mass-balance audits. Certifying agents
must demonstrate, as part of their
accreditation process, that any
inspectors or certification reviewers
they use have sufficient knowledge in
organic standards and practices to
successfully understand, verify, and
document an operation’s compliance or
noncompliance with the organic
regulations.
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The requirements in the rulemaking
are based on NOSB recommendations,
public comments, and the NOP’s own
experience auditing certifying agents.
AMS chose these specific skills because
they are essential to inspection and
certification review. These requirements
will ensure that inspectors and
certification review personnel can
accurately interpret the regulations and
standards, and consistently apply
critical skills when inspecting and
assessing compliance. This will address
the current regulation’s lack of specific
qualifications, experience, and
continual training for inspectors and
reviewers.
Certifying agents must also
demonstrate the expertise of all
personnel they use to conduct
inspection and certification review
(§ 205.501(a)(5)). Critically, this means
all inspection and review personnel
must have expertise in knowledge of
certification to the USDA organic
standards. Certifying agents must also
demonstrate their personnel must have
education, training, or professional
experience in the fields of agriculture,
science, or organic production and
handling that relates to assigned duties.
This requirement to demonstrate
expertise will facilitate more robust
accreditation audits of certifying agents
and ensure more consistent oversight of
certifying agents. Together with the
above knowledge and skills, this
requirement to maintain adequate
expertise will also promote
development of a uniform, high-quality
base of organic inspectors and
certification reviewers.
Training
Organic inspectors and certification
reviewers must complete regular
training relevant to their duties.
Training may include courses, webinars,
training sessions, field days, seminars,
conferences, shadowing other inspectors
on their inspections, and directed
readings on relevant topics. Certifying
agents may determine if specific
trainings fulfill the requirements.
Relevant training courses available on
the Organic Integrity Learning Center
(OILC) may also meet the annual
training requirements. When the
minimum training hours are completed,
certifying agents must still ensure that
each inspector and certification
reviewer has the training that is
sufficient to competently perform
assigned inspections or duties.
Sections 205.501(a)(4)(i)(B) and
205.501(a)(4)(ii)(B) require inspectors
and certification review personnel with
less than one year of experience to
complete at least 50 hours of training on
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USDA organic standards, inspection
protocols, and organic production and
handling practices. This requirement
will help ensure new inspectors and
certification review personnel are
adequately prepared for their duties.
The proposed rule had included a lower
number of hours across all staff, new
and experienced. Commenters suggested
that less-experienced staff require more
hours of training than existing staff.
AMS agrees with public comments and
has raised the initial training
requirement for less-experienced staff to
50 hours, which is a reasonable balance
that aligns with industry best practice
and will ensure staff are adequately
prepared to perform inspection and
certification duties.
Onboarding for new inspectors or
certification reviewers hired by
certifying agents may count towards the
50-hour requirement, as can other
qualifying training they complete in
their first year performing inspection or
certification review duties. Any
onboarding that counts towards the
training would need to be technical
rather than administrative to qualify as
relevant training. New inspectors must
complete the 50 hours of training, at
minimum, before they conduct
inspections independently. This allows
new inspectors to gain practical training
through shadow inspections. Training
requirements apply equally to
inspectors who are hired as employees
and contractors of certifying agents;
initial training received must
sufficiently address the scope and
complexity of work these personnel
encounter when performing their duties.
Sections 205.501(a)(4)(i)(B) and
205.501(a)(4)(ii)(B) detail training
requirements for inspectors and
certification reviewers with more than
one year of experience. Inspectors and
certification reviewers must complete
relevant ongoing training appropriate to
their existing skills, expertise, and scope
of work. The annual minimum is 10
hours per year for personnel inspecting
or reviewing one area of operation (i.e.,
crops, wild crops, livestock, and
handling). Five additional hours of
annual training are required for each
additional scope or area of operation.
For example, an inspector who only
inspects crop operations (i.e., a single
area of operation) must complete at least
10 hours of annual training; an
inspector who inspects crop, livestock,
and wild crop operations (i.e., three
areas of operation) must complete at
least 20 hours of training annually.
Because there are four scopes of
certification in the USDA organic
regulation (crops, livestock, handling,
and wild crops), the maximum number
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of training hours an inspector would be
required to complete annually would be
25 hours (10 hours of training for the
first scope of certification, plus 5 hours
for each of the additional 3 scopes of
certification).
AMS chose these training
requirements based on review of public
comment and review of established
industry norms. AMS agrees with public
comments that new inspectors will
require more robust initial training and
certifying agent personnel may require
more or less annual training depending
on how many areas of operation they
inspect or review. Therefore, relative to
the proposed rule, AMS is requiring 50
hours of training for new personnel, and
10 hours plus 5 hours per additional
area of operation for more experienced
inspectors.
AMS chose the 50-hour requirement
for new inspectors because it aligns
with industry best practice. Some
certifying agents commented that the
proposed 20-hour requirement for new
inspectors was adequate, while others
maintained that 75–100 hours was
necessary; 50 hours is a median within
that range. The 50-hour requirement
also aligns closely with the Accredited
Certifier’s Association’s ‘‘Guidance on
Organic Inspector Qualifications,’’
which recommends initial inspector
training that totals 43–46 hours plus
several mentored inspections and
monitored reports.37 Finally, many
certifying agents currently require new
inspectors to complete the International
Organic Inspector Association’s (IOIA)
basic training, a 5-day course requiring
approximately 40 hours to complete,38
plus additional field observation and
training that together total to 50 hours
of training.
AMS chose an annual training
requirement of 10 hours plus 5 hours
per additional scope for more
experienced inspectors because it is
consistent with standards established by
other agencies or organizations (e.g.,
Preventive Controls Qualified
Individuals per 2011 Food Safety
Modernization Act, ISO 9001 Global
Certified Lead Auditor), and because it
increases flexibility by allowing more or
less total annual training hours based on
the areas of operations inspected or
reviewed. These requirements will
ensure that inspectors and reviewers
receive annual training that is
37 ‘‘Guidance on Organic Inspector
Qualifications,’’ Accredited Certifiers Association,
Inc., February, 2018, https://www.accredited
certifiers.org/wp-content/uploads/2018/02/ACAGuidance-on-Inspector-Qualifications-with-IOIAEvaluation-Checklist.pdf.
38 IOIA Basic Training: https://www.ioia.net/
training-program-overview/.
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appropriate for the level and scope of
their duties.
In certain cases, certifying agents may
not be able to prescribe specific training
to contracted inspectors or certification
review personnel. However, certifying
agents must use a sufficient number of
qualified and trained personnel
(§ 205.501(a)(4)) and demonstrate that
all persons with inspection and
certification review responsibilities
have expertise in organic production
and handling (§ 205.501(a)(5). This
means that certifying agents must
ensure any contractor used to conduct
inspection or certification review
activities meets the training
requirements described in the
regulation.
Experience
In addition to training,
§ 205.501(a)(4)(i)(C) requires that
certifying agents demonstrate that the
inspectors they use have experience that
prepares them to conduct their assigned
duties. Certifying agents must
demonstrate that inspectors have at least
2,000 hours of relevant experience that
prepares them for the areas of operation
they will be assigned (i.e., crops,
livestock, handling, or wild crops). Both
this baseline experience requirement
and the 50-hour training requirement
must be met before inspectors can
independently inspect organic
operations. An experienced inspector
may advance to inspect more complex
operations based on performance.
The proposed rule specified one year
of experience. This was consistent with
the 2018 NOSB recommendation and
generally supported by public
comments. However, because public
comments noted that ‘‘one year’’ is
unclear and can be interpreted
differently, AMS has chosen a more
specific 2,000-hour requirement. This is
equivalent to one year of full-time work
(accounting for vacation and time off)
and expands the pool of qualifying
experiences because the hours can be
obtained across multiple years, from one
or more jobs, internships, or other
qualifying activities.
Eligible types of experience include
but are not limited to: work on a farm
or ranch; agricultural extension work;
agricultural education; internships;
apprenticeships; experiential education;
4–H; Future Farmers of America; other
inspection or auditing work;
management of an organic food
handling operation; food processing
research; or natural resource
management work. Qualifying
experience is not restricted to paid
work, and may include volunteer work
or education.
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This minimum experience
requirement is supported by
§ 205.501(a)(5), which requires that
certifying agents demonstrate that all
persons with inspection or certification
review responsibilities have education,
training, or professional experience that
relates to the duties they will perform.
Field Evaluation of Inspectors
Section 205.501(a)(6) requires
certifying agents to ensure that every
inspector they use is evaluated while
performing an inspection at least every
three years. Inspectors with less than
three years of organic inspection
experience must be evaluated every
year. The regulatory text refers to
observing an inspector while they are
inspecting an operation as a ‘‘witness
inspection.’’ This term is used by the
International Standards Organization to
refer to observations of inspections to
ensure proper adherence to inspection
procedures and the standards to which
the inspection is being made.
The rulemaking’s field evaluation
requirements are consistent with a 2016
NOSB proposal and accepted industry
guidance from the Accredited Certifiers
Association.39 In addition, public
comments supported this evaluation
frequency, including annual evaluations
for inspectors with less than three years
of inspection experience. The
rulemaking is therefore aligned with
industry best practice, and will ensure
that the performance of all inspectors is
consistently monitored and evaluated
by certifying agents.
The above requirement is a minimum
and certifying agents have the option of
conducting witness inspections more
frequently than the above guidelines to
verify an inspector’s ability to
successfully conduct inspection duties.
For example, certifying agents may
decide to conduct additional witness
inspections if there is a sudden change
in the complexity of an operation being
inspected, or if inspection reports show
deficiencies in an inspector’s skill or
knowledge.
To ease the burden on certifying
agents and inspectors, certifying agents
may share witness inspection reports
with each other, but each certifying
agent must demonstrate that they have
evaluated each inspector’s performance
in accordance with their own internal
39 ‘‘Personnel Performance Evaluations of
Inspectors’’ proposal, December 13, 2016: https://
www.ams.usda.gov/sites/default/files/media/
CACSInspectorsProposal.pdf.
The Accredited Certifiers Association, Inc. is a
501(c)(3) non-profit educational organization
created to benefit the accredited organic certifying
agent community and the organic industry: https://
www.accreditedcertifiers.org/.
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personnel policies and procedures.
Certifying agents may use employees or
contractors to perform the witness
inspections, provided they are qualified
to perform such duties (e.g., a witness
inspection for a diversified crop
operation should be overseen by an
evaluator with adequate experience in
inspecting diversified crop operations).
A key indicator of an individual’s
qualifications to conduct witness
inspections is whether that person can
perform the type of inspections they are
evaluating.
To ensure that witness inspections are
effective and consistent, certifying
agents must maintain procedures for
conducting and documenting them, and
maintain records of all witness
inspections of inspectors they have
conducted (§ 205.501(a)(6)(ii)). These
records may include a quantitative or
qualitative evaluation of the inspector,
along with details on where, when, by
whom, and on what area of operation
the inspection was conducted. This
requirement will facilitate more robust
accreditation audits and ensure more
consistent oversight of certifying agents.
Witness inspections are intended as
one tool to help certifying agents
maintain, evaluate and improve
inspector quality, but certifying agents
are also expected to take corrective
action appropriate to remedying gaps
and deficiencies in knowledge and
skills. For example, if a witness
inspection identifies problems with an
inspector’s report writing, then a desk
audit of additional inspection reports
may be appropriate to address any
shortcomings. Conversely, if an
inspector misses a significant
noncompliance while inspecting an
operation, the certifying agent may
decide to conduct a follow-up witness
inspection of the inspector.
Summary of Changes to the Final Rule
AMS made several changes to the
proposed regulatory text when writing
this final rule. Changes to the final rule
are discussed below and are followed by
responses to specific themes from
public comment.
• In § 205.501(a)(4)(i) and (a)(4)(ii),
AMS changed ‘‘scale’’ to ‘‘complexity’’
because public comments noted that
scale does not always equate to greater
complexity. AMS agrees with public
comments and included ‘‘complexity’’
in the rulemaking to highlight its
importance in determining appropriate
qualifications for inspectors and
reviewers.
• In § 205.501(a)(4)(i)(A) and
(a)(4)(ii)(A), AMS replaced ‘‘auditing’’
with ‘‘traceability audits’’ and ‘‘massbalance audits.’’ This addresses public
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comments that requested additional
specificity about the meaning of
‘‘audit.’’ The new language more closely
aligns with accepted and wellunderstood industry terminology and
more clearly describes the knowledge
and skills that certifying agents must
ensure their inspectors and reviewers
possess.
• AMS revised the proposed annual
training requirement of 20 hours in
§ 205.501(4)(i)(B) and (4)(ii)(B).
Inspectors and reviewers must complete
a baseline of 10 hours of training, plus
an additional 5 hours for each
additional area of operation they inspect
or review. Inspectors and reviewers
with less than one year of inspection
experience must complete 50 hours of
training within their first year. This
revised requirement is consistent with
established industry training standards
but is also more flexible because it
allows for more or less total annual
training hours based on the experience
of the inspector or reviewer and the
areas of operations they inspect or
review. This requirement will ensure
that inspectors and reviewers receive
annual training that is appropriate for
the level and scope of their duties.
• AMS updated proposed
§ 205.501(a)(4)(i)(C) from ‘‘field-based
experience related to both the scope and
scale of operations they will inspect’’ to
‘‘experience relevant to the scope and
complexity of operations they will
inspect.’’ We removed ‘‘field-based’’
because that term was unclear and
could be interpreted too narrowly.
Using ‘‘scope and complexity’’ focuses
the requirement on experience relevant
to the type of inspections to be
performed.
• AMS changed the one-year
experience requirement in
§ 205.501(a)(4)(i)(C) to 2,000 hours in
response to comments that requested
more specificity and a clear metric for
verifying compliance. A 2,000-hour
requirement is clearer, will promote
consistent implementation among
certifying agents, will allow inspectors
to combine qualifying experience from
more than one activity, and was
supported by public comments.
• In § 205.501(a)(6), AMS added
‘‘witness inspection’’ to refer to
certifying agents observing inspectors as
they inspect an operation. This change
aligns with industry and international
convention and more clearly describes
the requirement.
• AMS revised § 205.501(a)(6) to
clarify that certifying agents must
conduct annual witness inspections of
inspectors with fewer than three years
of experience. This change is consistent
with industry best practice and will
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ensure that the performance of new
inspectors is consistently monitored and
evaluated by certifying agents.
Summary of Public Comment
Many public comments focused on
the proposed number of required hours
of continuing education, with a mix of
comments that believed that 20 hours
annually is sufficient, and others
arguing that 20 hours would not be
sufficient. A few comments requested
flexibility in how inspectors meet the
education requirements, suggesting that
added flexibility would help them
complete the education more easily and
reduce costs for certifying agents.
Some comments expressed concern
that the proposed requirement of oneyear of field-based experience was
restrictive, and that the proposed rule
was not specific enough about what
types of experience would qualify. AMS
also received several comments noting
that using years as a metric is not an
adequate measure for experience;
several comments suggested a minimum
number of hours per year as an
alternative.
Several comments discussed
inspector evaluations, with most of
these comments supporting in-person
evaluations once every three years, and
others recommending more frequent
evaluations for new or inexperienced
inspectors.
Responses to Public Comment
Specified Additional Knowledge, Skills,
and Experience
(Comment) One comment stated that
labor laws prevent certifying agents
from requiring contract inspectors to
undertake specific training.
(Response) The regulations do not
require contract inspectors to complete
training specified by certifying agents;
however, certifying agents must
demonstrate that all inspectors,
including contract inspectors, complete
training that is relevant to inspection.
Certifying agents can recommend or
offer courses to contract inspectors, but
may not be able to require completion
of specific training courses. Certifying
agents should review inspector training
logs or other records to ensure that the
inspector has completed the required
number of hours and that the training is
appropriate to inspectors’ skill and role.
(Comment) Comments expressed
concern that a list of skills, knowledge,
and experience detailed in
§ 205.501(a)(4)(i)(A) may limit the pool
of organic inspectors, and thus limit the
capacity of certifying agents to inspect
operations. Comments stated that
specific qualifications should be based
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on the scope of inspections performed
by individual inspectors.
(Response) The list of qualifications
specified in this section are not unique
to any specific type of organic
operation, but are important for all
inspection and certification review
activities, regardless of area of
operation. All inspectors must meet the
general qualifications listed in
§ 205.501(a)(4)(i)(A). Specific
qualifications should be based on the
scope of inspections performed—
§ 205.501(a)(4) requires certifying agents
to demonstrate that inspectors have
qualifications to inspect the scope and
complexity of the operations assigned.
(Comment) Comments recommended
including recordkeeping, mass-balance
audits, traceability/trace-back audits,
DMI calculations, biosecurity, cultural
training, and internal control systems
for producer groups as areas where
inspectors must demonstrate adequate
knowledge and skills.
(Response) AMS expanded the list of
qualifications in the rulemaking to
include mass-balance audits and
traceability audits. These additions
support changes to the USDA organic
regulations for supply chain traceability
and on-site inspections as a result of
this rulemaking. DMI calculations,
biosecurity, and internal control
systems for producer groups are specific
to particular types of operations, and
AMS is not mandating these topics for
general organic inspector qualifications.
Although knowledge of recordkeeping is
not explicitly included, some certifying
agent personnel may need this
knowledge if it pertains to their duties
(e.g., personnel who conduct supply
chain traceability audits).
(Comment) Comments recommended
requiring special qualifications or
experience for inspectors who inspect
high-risk operations, including special
training requirements for producer
group operations.
(Response) AMS is not including
special training requirements for
inspectors of high-risk operations or
producer group operations. Section
205.501(a)(4)(i) requires certifying
agents to demonstrate that their
inspectors are qualified to inspect the
operations of the scope and complexity
assigned. If an inspector is to inspect
high-risk operations or producer groups,
then they must be qualified to inspect
those types of operations.
(Comment) Comments recommended
clarifying that import/export skills are
needed only if relevant, as not all
certifying agents deal with import or
export of organic products.
(Response) AMS is keeping import/
export requirements in the knowledge
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areas required for all inspectors.
Because this rule requires an NOP
Import Certificate for each organic
shipment imported to the United States,
all inspectors must have knowledge of
import and/or export requirements and
how they are implemented. Inspectors
who regularly inspect importing or
exporting operations, or operations
adjacent in the supply chain, may
require more advanced import/export
expertise.
Training Requirements
(Comment) Some comments stated
that an annual training requirement
violates labor laws regarding
contractors. Commenters claimed
certifying agents cannot provide the
training to contract inspectors, so these
inspectors will need to pay for the
training, which could lead to higher
inspection fees.
(Response) All inspectors must meet
the hourly annual requirements for
training that is relevant to their
inspection work. While certifying agents
cannot require inspectors to complete
trainings, certifying agents must ensure
all contract inspectors they use meet the
training requirement. The rulemaking
adds clarifying detail to existing training
requirements to ensure consistent
implementation by certifying agents. In
addition, there are various trainings
available for free, such as the online
Organic Integrity Learning Center,
which offers 33 courses averaging 3–4
hours per course. Additional no-cost
resources that could qualify for training
include resources published by
universities, the USDA, or other organic
experts (e.g., plant identification
databases, university extension courses,
recorded lectures, informational web
pages) and organic farming conferences.
Furthermore, certifying agents
commonly offer no-cost activities that
can count as training, such as updates
to inspection procedure, overviews of
changes in organic regulation,
supervised inspections, or field visits.
Because of the wide availability of nocost training, and because the rule’s
hourly training requirement is
consistent with what the industry
already practices, AMS does not believe
this requirement will result in
additional costs for inspectors beyond
what is accounted for the in the rule’s
economic analysis, or affect the cost of
inspection.
(Comment) Comments stated that the
number of required training hours
should depend on how many different
types of operations are inspected by a
particular inspector.
(Response) AMS revised the training
hour requirements in the rulemaking
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based on the types of operations
inspected—see § 205.501(a)(4)(i)(B) and
(a)(4)(ii)(B).
(Comment) Comments showed
concern that a specific numerical
training requirement is not appropriate.
They stated that the required content in
the training is critical, not the number
of training hours.
(Response) The annual training
minimum is required to ensure the
regulation’s specified knowledge, skills,
and experience requirements are
effectively implemented. Establishing a
minimum number of training hours sets
a clear baseline for inspector and
certification reviewer knowledge that
promotes consistent implementation of
the regulation by certifying agents.
Experience Requirements
(Comment) Comments opposed the
requirement that inspectors have one
year of field-based experience, asserting
it was difficult to interpret and may
limit the pool of potential inspectors.
(Response) AMS agrees that the
proposed use of ‘‘field-based’’
experience may be interpreted narrowly
(e.g., only farming and organic
inspection experience) and that this
may limit the pool of potential new
organic inspectors. The final rule is
updated to reference ‘‘relevant’’ rather
than ‘‘field-based’’ experience. This
change supports the use of a broader
pool of qualified candidates, such as
persons with auditing or food handling
experience.
(Comment) Comments recommended
changing the proposed requirement for
one year of experience to a specific
number of hours of related experience.
(Response) AMS incorporated this
recommendation into the final rule.
Inspectors are required to have at least
2,000 hours of relevant experience prior
to conducting their first inspection. This
is equivalent to one year of full-time
work, and can be obtained across
multiple years, from one or more jobs,
internships, or other qualifying
activities. This clarifies the requirement
and expands the pool of qualifying
experiences across an individual’s
career and education.
(Comment) Comments recommended
AMS adopt a ‘‘mentoring and evaluation
system’’ for inspectors in lieu of a oneyear field-based experience requirement
because the proposed requirement was
vague. Comments stated requiring
experience based on scope and scale
was seen as overly prescriptive and
would limit the pool of qualified
inspectors.
(Response) The rulemaking does not
codify an inspector mentoring program.
However, a mentorship program may be
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3583
used by a certifying agent to improve
the quality and proficiency of their
inspectors. Mentorships may also count
towards the 2,000-hour minimum
experience requirement, provided that
the certifying agent can demonstrate
that the mentorship provided
experience relevant to inspection.
Field Evaluation of Inspectors/Witness
Inspections
(Comment) Several comments
recommended that witness inspections
occur more frequently than once every
three years, or that NOP issue guidance
for how to determine when witness
inspections should be more frequent.
(Response) Certifying agents may
conduct witness audits more frequently
than once every three years ‘‘if
warranted.’’ However, certifying agents
must also maintain documented
policies, procedures, and records for
annual performance evaluations and
witness inspections (§ 205.501(a)(6)).
This means that a certifying agent may
choose to conduct witness inspections
more frequently than required by the
regulation (e.g., to monitor inspectors
with performance issues), but that the
reason for more frequent witness audits
should be justified and documented in
the certifying agent’s policies and
procedures.
Additionally, AMS increased the
frequency of witness inspections for
inspectors with less than three years of
experience from once per three years to
annually. This change was made to
ensure that the performance of new
inspectors is consistently monitored and
evaluated by certifying agents.
(Comment) Comments recommended
allowing virtual or remote witness
inspections.
(Response) Virtual and/or remote
witness inspections were not included
in the SOE proposed rule and AMS is
therefore not setting specific policy
related to virtual or remote witness
inspections. The final regulations
provide flexibility so that AMS may
consider virtual witness inspection
policy options in the future.
(Comment) Comments recommend
allowing certifying agents to share
inspector evaluation reports with other
certifying agents following witness
inspections.
(Response) AMS has addressed this
recommendation in the rulemaking.
Certifying agents may share witness
inspections reports with each other.
However, certifying agents using an
inspector performance evaluation or
witness inspection report from another
certifying must demonstrate that they
have evaluated the inspector’s
performance in accordance with their
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own internal personnel policies and
procedures.
(Comment) Several comments
expressed concern that the proposed
language would not allow contractors of
a certifying agent to perform witness
inspections.
(Response) Certifying agents may use
contractors to perform witness
inspections. However, the contracted
personnel performing the witness
inspection must be qualified to evaluate
the inspector (§ 205.501(a)(6)(i)).
(Comment) One comment stated that
new inspectors should be shadowed on
10 inspections during their first year, in
addition to the proposed 20-hour
training requirement.
(Response) AMS has not included this
recommendation in the rulemaking.
Witness inspections will assess
inspectors as they perform their duties,
with more frequent witness inspections
Section
205.2 ...................................
205.501 ...............................
205.665 ...............................
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I. Oversight of Certification Activities
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definition for Certification activity and Certification office.
General requirements for accreditation.
Paragraph (a)(22).
Noncompliance procedure for certifying agents.
Paragraph (a).
This rulemaking revises the USDA
organic regulations at §§ 205.2,
205.501(a)(22) and 205.665(a) to clarify
AMS’s authority to oversee the activities
of certifying agents. Certifying agents
must notify AMS when opening any
certification office that conducts
certification activities. In addition, this
rulemaking clarifies that AMS may issue
notices of noncompliance to certifying
agents based on the certification
activities of a party working on behalf
of a certifying agent.
Certifying agents, applicants for
accreditation, and certified operations
may be affected by these requirements.
Readers should carefully review the
regulations and policy discussion to
determine if they may be affected by
this action.
Background
Certifying agents commonly have
multiple offices to ensure they provide
adequate services to their clients.
However, certifying agents sometimes
open new certification offices without
reporting this to AMS. Some
certification offices operate
independently and in different
countries or regions than a certifying
agent’s main office. AMS cannot
provide oversight (regular audits and
reviews) or enforcement of offices of
which it is not aware. This can lead to
inconsistent application and
enforcement of the regulations across
certifying agents. To address these gaps
in oversight, the 2018 Farm Bill
amended OFPA to require certifying
agents to report new certification offices
to AMS within 90 days of opening.40
40 See section 10104(d) of the Agriculture
Improvement Act of 2018, Public Law No: 115–334,
available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf (7 U.S.C. 6515(j)).
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of less experienced inspectors.
Comments did not demonstrate the
benefit of shadowing, although
certifying agents may use this method if
it is documented in their policies and
procedures for witness inspections.
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AMS also needs clear authority to
initiate enforcement against parties
acting on behalf of a certifying agent
(e.g., a subcontractor) or individual
certification offices. The use of
subcontractors is common in the organic
industry and effective enforcement
depends on oversight of all persons
involved in the certification of organic
operations. Uncertainty about whether
AMS can target a certification office or
contractor for enforcement action
interferes with precise and expedited
enforcement. Therefore, AMS revised
the organic regulations to clarify that
entities acting on behalf of a certifying
agent are subject to oversight and
enforcement.
90-Day Notification of New Certification
Offices
To support the consistent application
of the organic regulations across all
certifying agents, § 205.501(a)(22)
requires certifying agents to notify AMS
within 90 calendar days of the opening
of any office performing certification
activities. A certification office is
defined as any site or facility where
certification activities take place, except
for activities that take place at certified
operations or other specialized facilities,
such as inspection, sampling, and
testing. This notification requirement
applies to any facility or location that
meets the definition of certification
office, regardless of how the office is
classified by a certifying agent (e.g.,
‘‘central’’ vs. ‘‘satellite’’ offices).
Notification of a new office opening
must include basic information to
support effective oversight of the
certification office, including the
countries serviced, location and nature
of the certification activities, and the
qualifications of the personnel that will
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provide the certification activities.
Information on the location of new
offices allows AMS to efficiently use
personnel and travel resources to
schedule on-site audits, and to be
precise in any adverse action that may
affect only a portion of certifying agent’s
accreditation, e.g., a certification office
or activities in a specific country or
region. Information on the types of
certification activities being conducted
allows AMS to better evaluate the need
for additional oversight; for instance, a
new office located in a high-risk area
with a history of organic fraud may
require additional oversight.
Authority To Issue Notices of
Noncompliance
AMS is clarifying its authority to
issue notices of noncompliance to
certifying agents based on the activities
of persons acting on behalf of a
certifying agent, the activities of a
certification office, or the activities in a
specific country. AMS added the term
certification activity to § 205.2 of the
organic regulations to define activities
that are essential to the function of a
certifying agent and therefore subject to
NOP oversight. Certification activity is
any business conducted by a certifying
agent, or by a person acting on behalf of
a certifying agent (e.g., a specific office
operating in specific countries, or a
subcontractor or subcontractor
organization). Any business activity
conducted by a certifying agent as it
implements the USDA organic
regulations is considered a certification
activity, including review, inspection,
and certification of organic operations.
The definition includes a nonexhaustive list of certification activities
that fall under AMS oversight authority.
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AMS’s authority to initiate
enforcement action for a portion of a
certifying agent’s operation is reinforced
in § 205.665(a)(1). This states that AMS
may send notifications of
noncompliance to a certifying agent
based upon review of the certification
activities of:
• A person acting on behalf of the
certifying agent or
• A certification office.
This means that AMS may issue
notices of noncompliance to a certifying
agent based on the activity of certifying
agent subcontractors, or an individual
certification office(s) that may be in a
different location from the certifying
agent’s main office. Further, AMS may
suspend or revoke a portion of
accreditation for activities in a specific
certification office, country, or region.
Summary of Changes to the Final Rule
AMS made no changes to the
proposed regulatory text in §§ 205.2,
205.501(a)(22), and 205.665(a) with
respect to oversight of certification
activities and has finalized the proposed
requirements.
Summary of Public Comment
The majority of public comments
supported AMS’s proposed clarification.
Commenters were primarily concerned
that the proposed definition of
certification office would subject remote
staff and home offices to NOP audits.
Commenters stated that NOP audits of
home offices and remote workers does
not align with NOP’s intent for adding
the term certification office. Comments
suggested excluding home offices and
telework locations from the definition
for certification office, and some
explained that certifying offices which
solely operate virtually should qualify
as a certification office and individual
workers working remotely on a
temporary basis should not be subject to
NOP audits.
Commenters were also concerned that
the 90-day timeframe for certifying
agents to notify AMS of new offices
conducting certification activities is too
long.
Responses to Public Comment
Definition of Certification Office
(Comment) AMS received comments
requesting that the definition of
certification office exclude home offices
and remote workers. Commenters
asserted that if home offices for remote
staff are included in the definition of
certification offices, they will be subject
to audits, which would be unreasonable.
(Response) Home offices are not
excluded in the definition of
certification office because some
certifying agents may maintain home
offices as their primary location or
certification office from which they
conduct certification activities.
90-Day Notification of New Offices
(Comment) We received comments
stating that the 90-day timeframe for
Section
205.2 ...................................
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205.511 ...............................
certifying agents to notify AMS of new
offices conducting certification
activities is too long. Some suggested
that timeframes of 30 or 45 days would
be more appropriate.
(Response) The 2018 Farm Bill
established the 90-day timeframe.
Section 10104 (j) of the 2018 Farm Bill
and 7 U.S.C. 6515(j) state ‘‘Not later
than 90 days after the date on which a
new certifying office performing
certification activities opens, an
accredited certifying agent shall notify
the Secretary of the opening.’’ While
certifying agents may choose to notify
AMS earlier, AMS is retaining the 90day notification requirement in the
organic regulations.
(Comment) Commenters asked what
office types (e.g., satellite offices or
main offices) would require a certifying
agent to notify AMS.
(Response) Certifying agents must
notify AMS of the opening of any type
of office where certification activities
take place. This requirement for
notification is based on the activities of
an office not the type.
J. Accepting Foreign Conformity
Assessment Systems
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definitions for Conformity assessment system and Technical requirements.
Accepting foreign conformity assessment systems.
Entire section.
AMS has added a new section to the
USDA organic regulations, § 205.511, on
accepting foreign conformity assessment
systems that oversee organic
certification in foreign countries.
Section 205.511 replaces former
§ 205.500(c).
Affected entities may include, but are
not limited to:
• Trade partners who have
established an organic equivalence
determination or are interested in
establishing an equivalence
determination with the United States.
• Foreign certifying agents and
certified operations not accredited or
certified by the USDA.
• Foreign organic producers who
export products to the United States.
The above list is a general description
of entities likely to be affected by this
action. Other types of entities could also
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be affected. You should carefully
examine the regulatory text to determine
if you or your organization may be
affected by this action.
Background
The OFPA, under 7 U.S.C. 6505(b),
allows imported organic products to be
sold or labeled in the United States as
organically produced if the Secretary
determines that the products have been
produced and handled under an organic
certification program with requirements
and oversight determined to be at least
equivalent to those described in the
OFPA. Under this authority, the U.S.
government, including the USDA and
the U.S. Trade Representative, work
closely together to implement processes
that determine the equivalence of
foreign organic certification programs
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and then negotiate an arrangement or
agreement as appropriate.
USDA organic regulations formerly
addressed USDA’s authority to make
equivalence determinations in general
terms under § 205.500(c), but did not
describe the criteria, scope, and other
parameters to establish, oversee, or
terminate such equivalence
determinations, which are critical to the
enforcement of organic imports. This
new § 205.511 does not change current
policy or add any new requirements. It
codifies existing practices and clarifies
the procedures followed when
determining organic equivalence, which
strengthens oversight and enforcement
capacity of organic imports by
supporting the government’s authority
to reassess, continue, and terminate
equivalence determinations, as
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necessary. Without this clear
implementation of Federal authority in
the USDA organic regulations, the
government could face challenges
establishing and enforcing terms under
current and future equivalence
determinations that are critical to
ensuring the integrity of imported
organic products.
Definitions
The rulemaking adds two new terms
in § 205.2: conformity assessment
system and technical requirements.
These terms are defined to ensure that
the process and requirements described
in § 205.511 are clear. The rulemaking
defines conformity assessment system as
all activities, including oversight,
accreditation, compliance review, and
enforcement, undertaken by a
government to ensure that the
applicable technical requirements for
the production and handling of organic
agricultural products are fully and
consistently applied. The rulemaking
defines technical requirements as a
system of relevant laws, regulations,
regulatory practices, standards, policies,
and procedures that address the
certification, production, and handling
of organic agricultural products.
Foreign Product Certification
Section 205.511(a) describes the U.S.
government’s authority under OFPA to
make equivalence determinations and
explains the conditions in which
foreign-produced product can be labeled
and sold as organic in the United States.
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Equivalency Determination Request
Section 205.511(b) describes the
process used by the U.S. government
and other foreign governments for
initiating a request for an equivalence
determination. Since there are several
factors that may impact whether the
U.S. government moves forward to
review an equivalence determination
request (e.g., agency resources, capacity
to oversee the potential trade
arrangement or agreement, relative
benefits for the U.S. organic sector), this
section clarifies that the U.S.
government will determine if it can
proceed with the evaluation process on
a case-by-case basis.
Equivalency Reviews and
Reassessments
Section 205.511(d) lays out the
current process that AMS and other
foreign governments use to monitor
equivalence determinations that have
been made. The section provides some
flexibility in the timing of reviews to
accommodate unavoidable factors in
both countries that can impact timing
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(e.g., federal budgets, election cycles,
growing seasons).
Equivalence Termination Procedures
Section 205.511(e) describes the
conditions under which the U.S.
government may terminate equivalence
determinations. These conditions for
termination are commonly accepted
among countries that maintain
equivalence determinations and are
based upon the core concepts
underlying equivalence. The U.S.
government must be able to terminate
equivalence determinations under these
conditions in order to fulfill its statutory
obligation to assure that organic
products sold in the United States are
compliant with OFPA and the USDA
organic regulations and maintain a level
playing field for U.S. farms and
businesses.
In addition to the conditions
described in § 205.511(e), the U.S.
government may also terminate an
equivalence determination ‘‘for other
good cause.’’ This includes risks that
may negatively affect the integrity of
organic products imported from a
country with which the U.S.
government has an equivalence
determination, policy changes, or
resource constraints that impact either
government. Examples include:
• Repeated cases of organic fraud that
are not corrected by a foreign
government;
• Increasing levels of organic fraud
that a foreign government is unable or
unwilling to address;
• Political instability, safety concerns,
or limitations on access that make it
impossible for USDA to travel to and
assess a foreign government’s
equivalence determination;
• Reduction in funding or other
resources that compromises a foreign
government’s or USDA’s ability to
operate its organic program and oversee
the equivalence determination; or
• Changes in a foreign government’s
unilateral equivalence determination
with the USDA that may restrict
domestic producers’ access to foreign
markets.
In all cases, the U.S. government
would provide notice and justification
to the foreign government prior to
termination, and give notice to affected
organic stakeholders along with a
reasonable timeline to transition.
Summary of Changes to the Final Rule
AMS made several revisions to the
proposed regulatory text when writing
this final rule. Changes to the proposed
rule are discussed below and are
followed by responses to specific
themes from public comment.
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• AMS added ‘‘oversight,
accreditation, compliance review, and
enforcement’’ to the definition of
conformity assessment system to clarify
the scope of the assessment of a foreign
organic certification system’s eligibility
for an equivalence determination.
• AMS added ‘‘standards, policies’’
and ‘‘certification’’ to the definition of
technical requirements to clarify the
scope of this term and to ensure that the
definition covers all parts of a country’s
framework for regulating organic
products.
• AMS corrected the syntax of
§ 205.511(a) and (b) to state that foreign
product ‘‘may be sold, labeled, or
represented in the United States as
organically produced.’’ This accurately
reflects the intent to allow foreign
organic product to be exported to the
United States and sold as organic, but
does not allow foreign organic product
to be labeled as domestically produced
in the United States.
• AMS removed the reference to a
two-year review cycle in § 205.511(d)
and replaced with a statement
explaining how AMS will determine the
timing and scope of reviews of
equivalence determinations. This gives
AMS the flexibility to determine
timelines for audits and reassessments
of equivalence determinations, and
allows AMS to accommodate
unavoidable factors when scheduling
audits and reassessments of equivalence
determinations.
Summary of Public Comment
Public comments showed overall
support for codifying AMS’s existing
practices for determining organic
equivalence, agreeing that the proposed
updates would strengthen the integrity
of imported organic products.
Several of these comments largely
focused on how the specifics of the
proposed § 205.511 would improve the
transparency and oversight of
equivalence determinations and
recognition agreements. Some of these
comments recommended requiring
certified foreign operations to be listed
in the Organic Integrity Database and for
NOP to investigate any countries with
equivalence determinations found to be
noncompliant. Some comments
expressed opinions in opposition to
some existing trade arrangements, and/
or suggested that USDA not allow
equivalence determinations and require
direct certification via USDA-accredited
certifying agents instead. Some
comments were also uncertain the
proposed requirements of § 205.511
apply to recognition agreements.
Several comments expressed concern
that the proposed § 205.511(a) and (b)
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would allow organic products produced
under foreign equivalence
determinations to be sold as ‘‘produced
in the United States.’’ Some comments
pointed out that the two and five-year
inspection timelines may conflict with
other regulations.
Responses to Public Comment
Definition of Conformity Assessment
Systems
(Comment) AMS received comments
requesting that several activities be
included in the definition of conformity
assessment systems. Commenters stated
that it is critical to ensure that foreign
governments have sufficient oversight,
accreditation, compliance, and
enforcement mechanisms in place to
ensure that organic technical
requirements are being enforced.
(Response) The definition of
conformity assessment systems has been
modified from the proposed rule to
include the following activities:
oversight, accreditation, compliance
review, and enforcement. The
additional activities were added to the
definition of conformity assessment
systems to clarify the scope of the
assessment of a foreign organic
certification system’s eligibility for an
equivalence determination.
Definition of Technical Requirements
(Comment) We received comments
requesting that the definition of
technical requirements include the
terms standards, policies, and
certification. Commenters stated that it
was important that these terms be added
to ensure that the definition covers all
parts of a country’s framework for
regulating organic products.
(Response) The terms standards,
policies, and certification have been
added to the definition of technical
requirements. The new terms were
added to ensure that the definition
covers all parts of a country’s framework
for regulating organic products.
Labeling of Foreign Product Origin
(Comment) Comments noted that
§ 205.511(a) could be interpreted to
allow labeling of foreign-produced
organic product as ‘‘produced in the
United States.’’
(Response) The final rule corrects the
syntax of § 205.511(a) to state foreign
organic product ‘‘. . . may be sold,
labeled, or represented in the United
States as organically produced.’’ This
accurately reflects the intent to allow
foreign organic product to be exported
to the United States and sold as organic,
but does not allow foreign organic
product to be labeled as domestically
produced in the United States.
Equivalence Reviews and
Reassessments
(Comment) We received comments
requesting AMS clarify its timeline for
audits and reassessments of equivalence
determinations. Additionally,
commenters noted the difference
between proposed § 205.511(d), which
requires a two-year midcycle review,
and the proposed rule preamble, which
states, ‘‘The review cycles mirror ISO
standards, which include a five-year
reassessment cycle and mid-cycle
reviews.’’
Section
205.660 ...............................
205.661 ...............................
205.100 ...............................
205.662 ...............................
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(Response) The final rule has been
revised to allow AMS additional
flexibility to determine timelines for
audits and reassessments of equivalence
determinations. The final rule replaces
‘‘two-year cycle’’ and ‘‘five years’’ with
the phrase ‘‘regular reviews and
reassessments.’’ The new regulatory
language allows AMS to accommodate
unavoidable factors when scheduling
audits and reassessments of equivalence
determinations.
(Comment) AMS received comments
asking if recognition agreements would
be subject to AMS audits and
reassessments per new § 205.511.
(Response) Recognition agreements
will be subject to AMS audits and
reassessments of equivalence per
§ 205.511.
Equivalence Determination Procedures
(Comment) We received comments
requesting AMS describe in § 205.511(e)
the criteria used to determine
termination of an equivalence
determination.
(Response) Each equivalence
determination is unique and is assessed
using the general criteria described in
§ 205.511. To ensure fair assessment of
each unique equivalence determination,
AMS has not codified specific criteria
used to determine termination of
equivalence.
K. Compliance and Noncompliance
Procedures
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
General.
Paragraph (c).
Investigation.
Change section heading only.
What has to be certified.
Paragraph (c).
Noncompliance procedure for certified operations.
Paragraphs (e)(3), (f)(1), and (g)(1).
Authority To Pursue Enforcement
Action Against Any OFPA Violator
The NOP currently pursues
enforcement actions against uncertified
parties when AMS has evidence of
OFPA violations. In 2021, more than
half of the complaints received by the
NOP alleging violations of OFPA
involved uncertified operations
representing products as organic.
Continued AMS enforcement against
uncertified operations is central to the
effective administration of the OFPA.
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The rulemaking updates the USDA
organic regulations by adding new
paragraph (c) to § 205.660, to clarify that
the NOP Program Manager may initiate
an enforcement action against any
violator of OFPA, regardless of
certification status. Consistent with the
new paragraph (c) to § 205.660, to
clarify that the NOP Program Manager
may initiate an enforcement action
against any violator of the OFPA, AMS
changed the title of § 205.661 from
‘‘Investigation of Certified Operations’’
to ‘‘Investigation.’’
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Enforcement Action Against
Responsibly Connected Persons
Person(s) responsibly connected to a
violator of the OFPA may be complicit
in the OFPA violation(s) because of
their association to the violator. Because
of this, the rulemaking clarifies at
§§ 205.100 and 205.662 that any person
who is responsibly connected to an
operation that violates OFPA or the
USDA organic regulations may be
subject to a suspension of certification,
civil penalties, or criminal charges and/
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or may be ineligible to receive
certification. This clarification
strengthens AMS’s enforcement
capacity by ensuring that enforcement
actions and penalties for violations of
the OFPA extend to all accountable
parties.
Responsibly connected persons who
are suspended or revoked may request
to have their certification reinstated, if
suspended, or their eligibility to become
certified reinstated, if revoked. AMS has
published guidance for Reinstating
Suspended Operations (NOP 2605),
which applies to both suspended and
revoked operations that want to become
certified again.41
Timely Updates to the Organic Integrity
Database
Timely updates to the Organic
Integrity Database (OID) are critical to
inform other certifying agents,
operations in the supply chain, and
consumers when an operation is no
longer certified and can help prevent
noncompliant products from entering or
continuing in the stream of commerce.
At § 205.662(e)(3) of the regulations,
AMS requires certifying agents to
provide timely updates on the status of
an operation that has been suspended or
revoked (or that has surrendered its
organic certification). These updates
should be viewable in the Organic
Integrity Database within three business
days of issuing a notification of
suspension or revocation, or from the
effective date of a surrender. This
publicly available information helps
businesses in the supply chain confirm
that an operation from which they
purchase or receive organic products
has a valid organic certification.
In most cases, the effective date of an
operation’s surrender means that the
certifying agent has received
notification from the operation and
confirmed the surrender status. AMS
recognizes that in some cases the
effective date of the surrender may date
prior to certifying agent confirmation of
surrender and the Organic Integrity
database updates will extend past the
three-day window.
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Federal Civil Penalty Inflation
Adjustment
Finally, AMS amended
§ 205.662(g)(1) of the regulations to
update the citation which specifies the
maximum civil penalty amount for
violations of the OFPA. Title 7 CFR
3.91(b)(1)(xxxvi) provides the civil
penalty amount for each violation of
41 Instruction NOP 2605, Reinstating Suspended
Operations: https://www.ams.usda.gov/sites/
default/files/media/2605.pdf.
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OFPA. This amendment aligns with the
Federal Civil Penalties Inflation
Adjustment Act Improvements Act of
2015, Public Law 114–74, sec. 701.42
Changes From Proposed to Final Rule
AMS made one change to the
proposed regulatory text when writing
this final rule:
• Removed the phrase ‘‘directly or
indirectly’’ from 205.660(c) because its
meaning was confusing. The intent of
205.660(c) is to clarify the scope of
potential enforcement actions which
may include blatant and subtle false
labeling and representation of
nonorganic products as organic.
No other changes were made to the
proposed regulatory text in
§§ 205.100(c), 205.660(c),
205.662(e)(3)), and 205.662(f)(1) and
AMS has finalized the proposed
requirements with respect to AMS’s
authority to enforce against any OFPA
violator and all responsibly connected
persons connected to a violator. AMS
also made no changes to proposed
requirement to timely update the
Organic Integrity Database.
Summary of Public Comments
In general, most public comments
supported the proposed revisions to
clarify AMS’s authority to enforce
against any violator of the OFPA and the
organic regulations. Many comments
also discussed the revisions in detail
and offered recommendations or
changes to the proposed policy.
Many comments discussed the
proposed three-day timeframe to submit
updates to the Organic Integrity
Database (§ 205.662(e)(3)). Some
comments describe the requirement as
too burdensome, while some support
the three-day timeframe. Comments
opposing the proposed requirement
recommended alternatives ranging from
7 to 30 days. Other comments state that
updates should be immediate, or made
within 48 hours, so that noncompliant
products do not continue in the stream
of commerce.
Several comments also claim that
identifying and tracking all responsibly
connected persons would be difficult,
and requested more guidance on how
this should be done. A few comments
asked AMS if revocation of an
operation’s certification should also
result in the revocation of all
42 https://www.govinfo.gov/content/pkg/PLAW114publ74/html/PLAW-114publ74.htm. As of the
publication of this rule the civil penalty amount is
$20,130 per violation of OFPA occurring on or after
February 15, 2022. The civil penalty amount will
be adjusted in the future so readers should refer to
7 CFR 3.91(b)(1)(xxxvi) for the current amount.
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responsibly connected persons’
certification.
Some comments also asked AMS to
clarify the phrase ‘‘or submit a request
for eligibility to be certified’’ in
§ 205.662(f)(1). A few comments also
asked if this applies to persons
responsibly connected to a suspended
operation. One comment also asked if
this section applies to revocation of
certification.
Responses to Public Comment
Timely Updates to the Organic Integrity
Database
(Comment) AMS received comments
that the three-day requirement to update
the Organic Integrity Database is too
burdensome. Commenters did not
quantify negative impacts to certifying
agents, nor did they clearly explain why
this would be burdensome for certifying
agents. Others supported the three-day
timeframe or recommended that updates
should be immediate or within 48
hours, so that noncompliant products
do not continue in the stream of
commerce. Other commenters
recommended alternatives ranging from
7 to 30 days.
(Response) Certifying agents will have
a one-year implementation period
before this requirement takes effect.
During the implementation period, there
is no fixed time frame for updating data
in the Organic Integrity Database. This
requirement is limited in scope and
applies when an operation is
suspended, revoked, or has surrendered
organic certification. Public accessibility
of an operation’s correct certification
status is essential for movement of
products in organic supply chains. AMS
believes that three days for certification
status updates is adequate and supports
organic verification across supply
chains of different speeds. Extending
the deadline beyond three days may
interfere with the timely verification of
an operation’s accurate certification
status. This is critical data and
inaccurate information can delay
legitimate transactions and fail to
prevent sales of products from
suspended or revoked operations.
Further, AMS provides certifying agents
with an API to upload data to the
Organic Integrity Database, which
reduces redundant or duplicative work
for certifying agents.
Enforcing Against Responsibly
Connected Persons
(Comment) AMS received comments
stating that identifying and tracking all
responsibly connected persons would
be difficult because these entities are
not listed in the Organic Integrity
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Database. Commenters requested
guidance on how this should be
accomplished.
(Response) AMS is not specifying
how certifying agents must identify
responsibly connected persons, nor are
we requiring responsibly connected
persons to be listed and searchable as
such in the Organic Integrity Database.
Obtaining responsibly connected
persons from organic system plans and/
or identifying all known responsibly
connected persons in adverse action
letters are best practices that certifying
agents should pursue.
Use of Term ‘‘Indirectly’’ in 205.660(c)
(Comment) Commenters requested
clarification of what is meant by a label
or information which ‘‘indirectly’’
implies that product was produced with
organic methods if product was
produced in violation of the OFPA or
the organic regulations.
(Response) AMS removed the phrase
‘‘directly or indirectly’’ from 205.660(c)
because its meaning was confusing. The
intent of 205.660(c) is to clarify the
scope of potential enforcement actions
which may include blatant and subtle
false labeling and representation of
nonorganic products as organic.
Civil Penalty Citation
(Comment) For civil penalty fines,
commenters requested AMS cite the
regulation, not the amount, since the
latter changes and becomes outdated.
(Response) The proposed and final
rules cite the regulation that sets the
civil penalty amount.
Documented Delivery Confirmation
(Comment) Commenters requested
AMS allow ‘‘documented delivery
Section
205.504 ...............................
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205.663 ...............................
confirmation’’ to accommodate
electronic communication rather than
only certified paper mail.
(Response) AMS accepts that ‘‘dated
return receipts,’’ which are required
when certifying agents or NOP sends an
adverse action notice to an operation,
may include electronic
communications. This means that the
adverse action notices may be sent
electronically to the recipient and
delivery confirmation may include, for
example, confirmation that an email has
been delivered.
L. Mediation
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Evidence of expertise and ability.
Introductory text and paragraph (b)(8).
Mediation.
Entire section.
Background
Mediation Is a Collaborative Process
AMS revised § 205.663 to improve the
general readability of this section and to
more clearly explain how mediation
may be used in noncompliance
procedures. When successful, mediation
is an efficient way to bring operations
into compliance and resolve conflicts
among certifying agents and operations.
The USDA organic regulations require
that certifying agents and State organic
programs provide applicants for
certification and certified operations the
right to request mediation when they
issue a denial of certification, notice of
proposed suspension, or proposed
revocation of certification (§§ 205.405(d)
and 205.662(c)). Section 205.663
provides requirements for requesting
mediation, responding to a mediation
request, the time frame for reaching an
agreement, and what happens when
mediation is unsuccessful.
The USDA organic regulations require
certifying agents and State organic
programs to notify operations of the
option to request mediation as an
alternative dispute resolution to resolve
noncompliance findings that have led to
a proposed suspension, revocation, or
denial of certification. This will
facilitate resolution of these issues
before they escalate to an appeal to AMS
or a State organic program.
The requirements for mediation
support a process that is efficient and
accessible to producers and handlers
who want to resolve a denial of
certification, proposed suspension, or
revocation of certification. Mediation is
a collaborative process between a
certifying agent and an operation or
applicant for certification. A successful
mediation addresses the
noncompliance(s) and leads to full
compliance with the USDA organic
regulations. To ensure that mediation is
readily accessible, certifying agents and
certified operations or applicants may
engage in mediation without a thirdparty mediator, provided that all parties
agree upon the person who will serve as
the mediator.
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Mediation Must Be Requested in
Writing
After a certifying agent issues a denial
of certification, proposed suspension, or
revocation of certification, a certified
operation and certifying agent may
discuss the option of mediation prior to
receiving a request for mediation.
However, for mediation to proceed as a
form of alternative dispute resolution,
an operation must request mediation in
writing to the certifying agent. The
request for mediation must be submitted
to the certifying agent within 30
calendar days from the date of the
proposed adverse action or denial of
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certification (§ 205.663(b)(1)). This
aligns with the length of time provided
to submit an appeal of a proposed
adverse action.
Mediation Acceptance Criteria
A certifying agent determines whether
to accept or reject a written request for
mediation. Certifying agents must
include mediation acceptance decision
criteria as part of the administrative
policies and procedures which
certifying agents are required to submit
to demonstrate their ability to comply
with the certification program
(§ 205.504(b)(8)). The mediation
acceptance criteria must be fair and
reasonable and not arbitrary. The
criteria must be based on factors that
will likely determine potential success
or failure of the mediation process. The
certifying agent must document how it
applied the criteria to accept or reject
requests for mediation. Parties to the
mediation may develop conditions,
such as cost, timeframes to reach a
settlement agreement within the
allowed maximum of 30 days, and any
incremental steps, only after a certifying
agent accepts a mediation request. A
certifying agent must not impose any
preconditions for the acceptance of
mediation (i.e., the certifying agent
cannot require that the operation take a
specific action—other than submitting a
written request for mediation—before it
will consider mediation).
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If a certifying agent decides to reject
a request for mediation, based on its
criteria for acceptance of mediation, it
must inform the operation in writing,
with the justification for the rejection.
That notification must explain that the
operation has the right to appeal the
rejection of mediation (§ 205.663(b)(3)).
While an operation appeals a rejection
of mediation, the proposed suspension
or revocation which led to the request
for mediation must not be finalized
(§ 205.663(b)(4)). The date that the
notification is received by the operation
is important because it starts the 30-day
window for filing an appeal and may be
used to determine whether an appeal
has been timely filed. Likewise, when
mediation is unsuccessful, the certifying
agent must inform the operation in
writing to document the start of the 30day window for filing an appeal. This
means that certifying agents must send
rejection and termination of mediation
notices using a method with delivery
confirmation.
Use of Settlement Agreements
In accepting mediation, a certifying
agent may also, at its discretion, offer a
settlement agreement for an operation to
consider (§ 205.663(e)). The outcome of
successful mediation is a settlement
agreement that brings an operation into
compliance with the USDA organic
regulations. A settlement agreement
must clearly describe the corrective
actions and timeframes for
implementing corrective actions, and
may impose additional actions (e.g.,
unannounced inspections, sampling for
residue testing) to ensure the operation
maintains compliance. A settlement
agreement may also include a
suspension of organic certification.
A settlement offer may be useful
when the corrective action(s) is clear
and the noncompliance(s) is not
recurrent. As part of the mediation, an
operation may accept or reject the
settlement agreement, negotiate the
terms with the certifying agent, or
request a mediator to try and reach a
settlement agreement.
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Use of a Third-Party Mediator
This rule clarifies that mediation does
not require a third-party mediator to
reach a settlement agreement
(§ 205.663(c)). The certifying agent and
operation may agree that mediation will
be between only those two parties. For
example, mediation may consist of a
phone call or series of phone calls
between the operation and the certifying
agent to discuss the terms of a
settlement offer prior to signing the
agreement.
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In some cases, the use of a third-party
mediator may be appropriate, either
because the operation initially requested
this, or the operation rejected a
settlement offer and then requested a
mediator. To demonstrate their ability to
comply with the certification program,
each certifying agent must submit a
process to identify a qualified mediator
and set the time and location of
mediation session(s), mediation format
(in-person, video, phone), and
mediation fees and payment
(§ 205.504(b)(8)).
Role of the Program Manager
The Program Manager does not
require, manage, or otherwise
participate in mediation between
operations and certifying agents or State
organic programs. The Program Manager
may review an agreement that results
from the mediation for conformity to the
OFPA and the USDA organic
regulations and reject any
nonconforming provision or agreement
(§ 205.663(f)). The Program Manager
may direct the certifying agent or State
organic program to revise any
nonconforming provisions, and the
operation would have a new
opportunity to accept or reject the
revised settlement agreement.
Mediation under the USDA organic
regulations is an alternative dispute
resolution mechanism, conducted
between a certified operation or
applicant for certification and a
certifying agent or State organic
program. The Program Manager is not
involved in determining the outcome of
a mediation, notwithstanding his or her
authority to review dispute resolution
terms for conformity with the OFPA and
the USDA organic regulations.
This does not affect AMS’s ability to
carry out oversight, compliance, and
enforcement activities on behalf of the
Program Manager. For example, AMS
may conduct informal mediation, at its
discretion, and enter into mutually
agreeable settlement agreements with
parties that receive a proposed adverse
action (§ 205.663(g)).
Changes From Proposed to Final Rule
AMS made minor revisions to the
proposed regulatory text when writing
this final rule. Changes to the final rule
are discussed below and are followed by
specific themes from public comment.
• AMS added the words ‘‘of receipt’’
to § 205.663(b)(3) and (e) so that the 30day time frame for requesting an appeal
when mediation is rejected or
terminated provides adequate due
process and aligns with the appeal filing
time frame for other adverse action
notices.
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• AMS added a requirement for
termination of mediation to be
documented in a written notice so it is
clear when an operation may exercise
its right to file an appeal.
• AMS revised the introductory
paragraph at § 205.504 to include the
cross-reference to § 205.663 because
certifying agents must submit mediation
procedures as part of the evidence of
their ability to comply with and
implement mediation requirements.
• AMS relocated the requirement to
submit mediation policies and
procedures from § 205.663(a) to
§ 205.504(b), where requirements for
certifying agents’ policies and
procedures are identified.
• AMS added a requirement that
certifiers document the reason for
denying mediation. If the rejection is
appealed, this will allow the
Administrator to determine whether the
rejection was reasonable and consistent
with the certifier’s criteria for rejection.
• AMS added the word ‘‘reasonable’’
to § 205.504(b)(8) to describe parameters
for the criteria that certifiers must set for
accepting mediation. This supports fair
and consistent decisions on requests for
mediation across certifying agents.
• AMS revised § 205.663(e) to require
that a settlement agreement be reached
within 30 days from the start of
mediation. This clarifies when the 30day timeframe begins and supports
timely resolution of compliance issues.
• AMS added a new provision at
§ 205.663(b)(4) to clarify that an adverse
action (e.g., proposed suspension or
revocation) must not be finalized during
the appeal proceeding. This clarification
supports the right to adequate due
process before an adverse action takes
effect.
Responses to Public Comment
Settlement Agreements
(Comment) Several commenters asked
questions about the management of
settlement agreements.
(Response) AMS is not addressing
questions about management of
settlement agreements in this rule
because they are beyond the scope of
this rule. More information on
settlement agreements is available
through the Organic Integrity Learning
Center and annual training for certifying
agents.
Mediation
(Comment) AMS received a comment
stating certifying agents should be
allowed to propose mediation and offer
settlement agreements.
(Response) The regulations do not
prohibit a certifying agent from
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informing an operation of its
willingness to engage in mediation prior
to an operation requesting mediation. In
addition, the regulations do not prohibit
a certifying agent from offering a
settlement agreement as part of
mediation to resolve an adverse action.
(Comment) AMS received a comment
to replace the terms ‘‘mediation
session’’ with ‘‘mediation’’ to allow
informal mediation at § 205.663(e).
(Response) AMS replaced ‘‘mediation
session’’ with ‘‘mediation’’ to account
for informal mediation which may not
use the same format as formal
mediation.
(Comment) AMS received a comment
to change the deadline to submit a
request for mediation from ‘‘30 days
from receipt’’ to ‘‘30 days from date of
issue.’’
(Response) AMS is declining to make
this change, in order to align with
USDA’s Office of Administrative
Hearings and Appeals, which uses date
of receipt and not date of issue. This
practice preserves due process rights of
operations being notified of adverse
actions. AMS believes that the use of
electronic communications and the
availability of electronic delivery
confirmation will make this requirement
less burdensome.
(Comment) Comments requested that
AMS align language for timeframes for
requesting mediation and requesting an
appeal.
(Response) AMS agrees that the
timeframes for requesting mediation and
requesting an appeal when mediation
fails should be consistent. We changed
§ 205.663(b)(3) to state that an operation
has 30 days from receipt of the rejection
of request for mediation to file an
appeal. We also changed § 205.663(e) to
state that an operation has 30 days from
Section
205.2 ...................................
205.680 ...............................
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205.68 .................................
receipt of a written notice of termination
of mediation to file an appeal. These
changes make the timeframes to file an
appeal consistent whether mediation is
rejected or terminated.
(Comment) AMS received a comment
that both parties agreeing on the person
conducting mediation should only
apply to formal mediation.
(Response) AMS disagrees that
consensus on the person conducting
mediation should only apply for formal
mediation. Informal mediation also
requires that parties agree on who will
facilitate the mediation, even when the
parties to the mediation facilitate the
process themselves.
M. Adverse Action Appeal Process
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definition for Adverse action.
Adverse Action Appeal Process—General.
Entire section.
Adverse Action Appeal Process—Appeals.
Paragraphs (a), (a)(2), (b), (c), and (d)(1) and (2).
General Appeals
AMS revised parts of the adverse
action appeals process in §§ 205.680
and 205.681. These changes clarify
which actions can be appealed,
recognize the use of alternative dispute
resolution in lieu of a formal
administrative proceeding to resolve an
appeal, and reinforce that appeal
submissions need to comply with the
basic requirements in the regulations.
The OFPA calls for an expedited
appeals procedure that gives persons
affected by a proposed adverse action
the opportunity to appeal that action (7
U.S.C. 6520). All appealed adverse
actions are expeditiously reviewed and
decided in an unbiased manner by
persons that are not involved in the
initial decision to issue an adverse
action. In December 2014, AMS issued
guidance to explain how it administers
the adverse action appeal process, the
status of an appellant during an appeal,
and the possible outcomes of an appeal
in NOP 4011, Adverse Action Appeal
Process.43
The original USDA organic
regulations described how certified
operations, accredited certifying agents,
and applicants for certification or
43 NOP
4011, Adverse Action Appeal Process.
December 23, 2011: https://www.ams.usda.gov/
sites/default/files/media/4011.pdf.
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accreditation may appeal a
noncompliance decision that would
affect their certification or accreditation
status or eligibility to become certified
or accredited (§ 205.680(a)). The
regulations explained when an appeal
may be submitted, how it must be
submitted, and what the appeal
submission must contain. Specifically,
appeals of noncompliance decisions of
a certifying agent or NOP are appealable
to the AMS Administrator, or to the
State organic program if the appellant is
in a State with an approved State
organic program. A decision to sustain
an appeal will result in a favorable
action with respect to the appellant’s
certification or accreditation. Following
a decision to deny an appeal, AMS will
initiate a formal administrative
proceeding (i.e., a hearing), unless the
parties resolve the issue through
settlement, or the appellant waives the
hearing. If an appeal is not timely filed,
the adverse action which led to the
appeal will be final and cannot be
appealed further.
Adverse Action Defined
The new term adverse action clarifies
which actions may be appealed under
the USDA organic regulations. Adverse
action replaces the use of
‘‘noncompliance decision’’ throughout
this section. Adverse action is defined
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as a noncompliance decision that
adversely affects certification,
accreditation, or a person subject to the
Act, including a proposed suspension or
revocation; a denial of certification,
accreditation, or reinstatement; a ceaseand-desist notice; or a civil penalty.
Option To Request Mediation or Appeal
of an Adverse Action Issued by a
Certifying Agent or State Organic
Program
When a certifying agent or State
organic program issues a proposed
suspension or revocation, operations
have the option to request mediation or
appeal the proposed adverse action.
Mediation is covered in more detail in
§ 205.663. The mediation process can be
a viable path to resolve noncompliances
that are correctable and are not willful
or recurrent. If mediation is rejected or
is not successful, the operation
maintains the right to appeal. The time
frame for filing an appeal is calculated
from receipt of the notice of rejection or
termination of mediation
(§ 205.663(b)(3) and (e)).
Administrative Requirements
Appeals must be properly filed as
described in paragraphs (c) and (d) of
§ 205.681. This means that an appeal
must be:
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• Filed in writing within the time
period provided in the letter of
notification or within 30 days from
receipt of the notification, whichever
occurs later.
• Sent to the correct physical or email
address:
Æ 1400 Independence Ave. SW, Room
2642, Stop 0268, Washington, DC
20250.
Æ NOPAppeals@usda.gov.
• Include a copy of the adverse action
and explain why the adverse action is
incorrect.
An adverse action will become final
and nonappealable unless an appeal is
timely filed. Appeals will be considered
‘‘filed’’ on the date received by the
Administrator or by the State organic
program.
Denied Appeals
AMS supports the use of alternative
means, such as mediation and
settlement agreements to expedite
resolution of an adverse action dispute
while preserving due process and
avoiding prolonged formal proceedings.
When an appeal is denied, AMS offers
the appellant the option to waive further
hearing. When an appellant waives a
hearing, the appeal decision is final and
takes effect. Failing to timely submit a
request for hearing is regarded as a
waiver of hearing. In some cases, when
an appeal is denied, AMS may pursue
a settlement agreement in lieu of
initiating a formal administrative
proceeding. AMS assesses the potential
for a settlement agreement on a case-bycase basis and will exercise this option
when a settlement may offer a viable
route for the operation to come back
into compliance or to exit the organic
sector. Even when an appellant requests
a hearing, AMS and the appellant may
enter into a settlement agreement prior
to the hearing. This provides flexibility
to resolve appeals outside of a lengthy
formal administrative process. The
appellant reserves the right to an
administrative hearing. Entering into a
settlement agreement is an optional, not
compulsory, alternative to a hearing.
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Changes From Proposed to Final Rule
AMS made several revisions to the
proposed regulatory text when writing
this final rule, including revising
§ 205.681(a)(2) and (b)(2) to state that
the Administrator will initiate a formal
proceeding and identify the conditions
when that would not occur, i.e., the
parties settle beforehand, or the
appellant waives its right to a hearing.
These sections explain that failing to
timely request a hearing constitutes a
waiver of hearing. AMS also deleted
‘‘policies and procedures’’ from
205.681(d)(3) to clarify that the USDA
organic regulations are the basis for
enforcement.
Summary of Public Comments
Comments were generally supportive
of the clarifications to the appeals
sections of the USDA organic
regulations. The main concern in
comments was the revision to state that
AMS ‘‘may’’ rather than ‘‘will’’ initiate
a formal administrative proceeding if
the Administrator denies an appeal. The
comments stated that this change
removes due process rights of an
appellant and should not be at the
discretion of AMS. Other comments
requested changes to appeal filing
timeframes and delivery confirmation.
Responses to Public Comment
(Comment) Comments opposed the
change to not require AMS to initiate
the hearing process following an appeal
denial.
(Response) AMS made changes to
§ 205.681(a)(2) and (b)(2) to state that
AMS will begin formal administrative
proceedings once an appeal is denied.
Those sections also explain that an
administrative proceeding would not
begin if the appellant waives or fails to
timely request a hearing or AMS and the
appellant reach a settlement agreement.
This revision does not change AMS’s
intent that appellants always have the
right to request a hearing following a
denial of an appeal; it only provides
options for a more expedient resolution
in lieu of a hearing if the appellant
consents to that outcome.
(Comment) AMS received comments
stating that the proposed revisions to
§ 205.681(b) do not clearly provide
appeal rights for certifying agents.
(Response) Person, as defined in the
regulations at § 205.2, includes
certifying agents and § 205.681(b) allows
persons to appeal an adverse action by
the NOP Program Manager. Further,
§ 205.681(b)(1) explains what happens
to accreditation when an appeal is
sustained.
(Comment) AMS received comments
suggesting that dated return receipts
should be replaced with documented
delivery confirmation.
(Response) AMS interprets dated
return receipts to include electronic
confirmation of electronic delivery,
such as registered email which shows
that a message has been delivered to
recipient’s email and the date of
delivery.
(Comment) AMS received comments
that appeals should be filed within 30
days of date of notice rather than date
of receipt of notice.
(Response) AMS is not making this
change because it could interfere with
due process rights of an appellant. We
believe that appellant should have the
full 30 days to appeal from the time that
they receive the notice and not lose time
due to possible delays in the mail or
delivery service. Therefore, we are
keeping this timeframe to 30 days from
the date of receipt of notice to ensure
that appellants have 30 days to review
the notice and to decide how to
respond.
(Comment) Comments requested that
NOP timely respond to appeals because
operations are allowed to remain
certified during the appeal process and
any subsequent hearing proceeding.
(Response) AMS has procedures to
thoroughly and efficiently evaluate NOP
appeals. AMS generally resolves appeals
within 6 months of receipt. AMS also
frequently uses settlement agreements to
resolve appeals which decreases the
number of appeals that may potentially
proceed to a hearing.
N. Producer Group Operations
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Section
Final regulatory text
205.2 ...................................
Terms defined.
Definitions for Producer group member, Producer group operation, Producer group production unit, and Internal
control system.
Organic production and handling system plan.
Paragraph (c).
General requirements for certification.
Paragraph (g).
On-site inspections.
Paragraph (a)(2).
205.201 ...............................
205.400 ...............................
205.403 ...............................
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Federal Register / Vol. 88, No. 12 / Thursday, January 19, 2023 / Rules and Regulations
The organic industry has a
longstanding practice of certifying
groups of producers. This practice helps
small farmers access the organic market
and enables handlers to source products
that are not produced in the United
States. Compared with traditional
producers and handlers, these groups of
producers have unique needs in quality
control and compliance. AMS is
establishing requirements for producer
group operations that promote
consistent certification practices and
ensure their continued viability and
integrity. This rule codifies key
provisions of the 2002 and 2008 NOSB
recommendations on producer group
certification, including:
• Establishing eligibility criteria for
operations to qualify as producer group
operations.
• Clarifying the function and
responsibilities of Internal Control
Systems (ICS).
• Clarifying inspection requirements
for producer group operations.
Additionally, this rule builds upon
the NOSB recommendations with
additional detail based on public
comment and NOP’s programmatic
experience auditing certifying agents
and witnessing producer group
inspections. These additions include
requirements for more specific ICS
requirements, more specific member
and group information in OSPs, and an
improved inspection sampling rate.
This rule strengthens the oversight of
organic supply chains by enabling
certifying agents to more readily assess
a producer group operation’s
compliance with the USDA organic
regulations. Certifying agents and
operations that are certified as part of a
producer group may be affected by these
requirements. Readers should carefully
review the regulatory text and policy
discussion to determine if the
requirements apply to them.
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Background
Producer group operations export
important organic agricultural products
to the United States, such as coffee,
cocoa, bananas, tea, and spices.44
Globally, there are about 2.6 million
organic producers organized across
5,900 producer group operations in 58
countries (mainly in Africa, Asia, and
Latin America), managing a total area of
44 Producer
groups may also be called ‘‘grower
groups.’’ The latter term is commonly used when
certification of group operations is limited to the
production or harvest of crops or wild crops.
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about 4.5 million hectares (11 million
acres) of certified organic land.45
Producer group operations present
unique certification challenges.
Producer groups may have thousands of
members spread across a large area. The
collection, handling, and processing of
crops may be centralized, and these
groups may also rely on centralized
input procurement, training, and
marketing to sell their product. These
centralized practices can introduce risks
to traceability and organic integrity due
to producer group operations’ unique
structure, size, and reliance upon
internal quality control systems (the
ICS) as the first layer of oversight.
Through certification audits and field
visits, USDA has witnessed many of the
common problems created by the lack of
a codified producer group standard.
The most common, and difficult to
address, challenge is lack of a wellfunctioning ICS. The ICS is the first line
of oversight and enforcement and is
responsible for critical functions such as
education and inspection of members,
and ensuring adherence to the organic
regulations. A poorly functioning ICS
often leads to poorly trained members
who do not understand basic organic
principles, and the ICS’s lack of
effective oversight means members’
mistakes go unreported, resulting in a
breakdown of the basic oversight
necessary to ensure that products meet
the USDA organic standard. As a result,
NOP audits have uncovered issues such
as application of prohibited synthetic
fertilizers and pesticides, mixing of
conventional and organic products,
decentralized storage that causes mixing
and contamination, and poor or
nonexistent recordkeeping that makes
traceability and verification of integrity
difficult. These issues sometimes persist
because the current regulations lack ICS
responsibilities and NOP therefore has
no mechanism or basis for citing
noncompliance.
Conflict of interest can also become a
challenge if not specifically addressed
by the ICS. Often, ICS personnel are
relatives or friends of the members and
may withhold or obscure evidence of
noncompliance or fraud. In other cases,
the influence of a buyer or exporter will
lead members to compromise organic
45 Florentine Meinshausen, Toralf Richter, Johan
Blockeel and Beate Huber Project: Consolidation of
the Local Organic Certification Bodies—ConsCert
(2014–2018)//March 2019 https://orgprints.org/id/
eprint/35159/7/fibl-2019-ics.pdf.
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3593
integrity in order to meet specific
quality or volume targets.
In addition to the ICS, the lack of
general criteria that producer groups
must meet creates challenges for
certifying agents. This is most often seen
as an absence of critical information
about the producer group and its
members. Producer groups often do not
provide certifying agents with basic
information, such as accurate maps,
location of plots, acreage, and
production practices and inputs. During
inspection, certifying agents commonly
cannot locate members, plots,
boundaries, or central distribution
points, making it difficult to complete
basic audit techniques such as yield
analysis or mass balance.
The unique conditions of producer
group production mentioned above,
when combined with poor oversight and
enforcement mechanisms at the ICS
level, create an environment where loss
of organic integrity and organic fraud
are more likely to occur. The organic
regulation currently does not have the
specificity to address these unique
challenges, making it challenging to
both discover and correct issues that are
prevalent in producer groups. The
provisions in this rule codify specific
eligibility criteria, ICS requirements,
and inspection techniques to address
these challenges, and the rule will give
certifying agents the ability to
successfully certify and oversee
producer group operations and the
products they produce.
The International Federation of
Organic Agriculture Movements
(IFOAM) 46 started developing criteria
for producer group certification in 1994,
and in 2003 published its position on
‘‘Small Holder Group Certification for
organic production and processing’’ to
support the concept.47 The criteria
formed the basis for acceptance of
producer group certification in the
European Union (EU) and the United
States. Producer group operation
certification is also used by other
standards organizations, such as the
International Accreditation Forum and
Global G.A.P., to provide small-holder
farming operations access to markets,
expand consumer choices, and ensure
the integrity of the supply chain.48
46 https://www.ifoam.bio/.
47 https://www.ifoam-eu.org/sites/default/files/
page/files/small_holder_group_certification_0.pdf.
48 https://www.iaf.nu/; https://
www.globalgap.org/uk_en/.
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Organic certification standards for
producer group operations support
strong and consistent oversight and
enforcement of producer group
operations. This final rule addresses
2002 and 2008 NOSB recommendations
on producer group certification and
adds detail about documentation
requirements and inspection methods in
response to public comments to the
proposed rule.49 While there are only a
few known producer groups in the U.S.
at this time, setting requirements for
producer groups may help U.S.
producer group members access the
organic cost-share program and crop
insurance. These regulations support
the legitimate status of U.S. producer
group members as part of an organic
operation.
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Qualifying as a Producer Group
Operation
Certifying agents must assess whether
operations that apply for or maintain
producer group certification meet the
characteristics in the definitions for
producer group member, producer
group operation, and producer group
production unit and the qualifications
for certification as producer group
operations in 205.400(g). Operations
that do not meet all criteria must not be
certified as a producer group operation.
The smallest unit of a producer group
operation is a producer group member.
A producer group member is an
individual engaged in the activity of
producing or harvesting agricultural
products as a member of a producer
group operation. The practices of each
producer group member must align with
the organic system plan (OSP) of the
producer group. Each member must use
practices that comply with the
requirements for producers and
handlers in the USDA organic
regulations. Some requirements may be
met collectively by the producer group
operation, such as submitting an organic
system plan.
Producer group members are
organized into production units. A
producer group production unit is a
defined subgroup of producer group
members in geographic proximity
within a single producer group
49 NOSB Recommendation: Criteria for
Certification of Grower Groups. October 20, 2002:
https://www.ams.usda.gov/sites/default/files/
media/Rec%20Criteria%20
for%20Certification%20of
%20Grower%20Groups.pdf.
NOSB Recomendation: Certifiying Operations
with Multiple Production Units, Sites, and
Facilities under the National Organic Program.
November 19, 2008: https://www.ams.usda.gov/
sites/default/files/media/NOP%20Final%20
Rec%20Certifying%20Operations
%20with%20Multiple%20Sites.pdf.
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operation that use shared practices and
resources to produce similar agricultural
products. Each producer group
operation determines the producer
group production units in its operation
and must identify these in the organic
system plan per § 205.201(c)(4).
A producer group operation is a
producer, organized as a person,
consisting of producer group members
and production units in geographic
proximity governed by an internal
control system under one organic
system plan and certification. A
producer group operation must define
its geographic proximity criteria for its
producer members and production units
§ 205.201(c)(4). The site-specific
conditions of an operation, such as
infrastructure, topography, common
soil, water source, and products
produced will affect ‘‘geographic
proximity.’’ Therefore, AMS is requiring
that certifying agents document and
adopt their own criteria or guidelines
for internal consistency when
establishing acceptable distances or
evaluating the geographic reach of a
producer group operation.
Producer group operations may be
certified for crops, wild crops, livestock,
and handling. The requirements for
production and handling operations in
the USDA organic regulations also apply
to producer group operations.
Structure and Organization of Producer
Group Operations
A producer group operation must be
organized as a person (§ 205.400(g)(1)).
Organization as a person provides a
path to certification because OFPA and
the USDA organic regulations apply to
a person as the basic regulatory unit.
The definition for person at 7 U.S.C.
6502(16) and § 205.2 includes groups
(e.g., ‘‘. . . association, cooperative, or
other entity’’). Therefore, certification
may be granted to the producer group
operation, rather than individual
producer group members.
A producer group operation must use
centralized processing, distribution, and
marketing facilities and systems
(§ 205.400(g)(2)). A group may have
several facilities for aggregating the
products of producer group members
and production units and moving into
commerce.
An internal control system (ICS) is a
defining component of producer group
operations and is critical for
management of the operation. The ICS
is an additional tier of oversight and
enforcement between the producer
group members and the certifying agent.
All producer group operations must
have an ICS that implements the
practices and procedures described in
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the organic system plan
(§ 205.400(g)(4)). Further ICS
requirements are discussed in the
following section.
All products sold, labeled, or
represented as organic by a producer
group operation must be produced or
harvested only by producer group
members on land and using facilities
that are included in the producer group
operation’s certification
(§ 205.400(g)(5)). This means that, for
example, a producer group member
from one operation (A) must not use a
handling facility owned by another
producer group operation (B) unless the
facility is included in the organic
system plan and the producer group
operation’s (A) certification. A producer
group operation must not buy products
from non-member producers and sell,
label, or represent them as organic using
the producer group certification.
Likewise, producer group members
must not sell, label, or represent their
products as organic outside of the
producer group operation unless they
are individually certified
(§ 205.400(g)(6)). This accommodates
producer group operations with
members of varying production levels
where some members have the capacity
and need for marketing channels in
addition to the producer group
operation. When this occurs, clear and
careful recordkeeping is essential for
successful mass-balance audits.
Producer group operations must
provide a comprehensive inventory of
the producer group operation and its
capacity to the certifying agent.
Specifically, the operation must provide
the name and location of each producer
group member and producer group
production unit(s), and identify all
products produced, estimated yield(s),
and the sizes of the production and
harvesting areas (§ 205.400(g)(7)).
Producer group operations must provide
this information to the certifying agent
at least annually and should inform the
certifying agent more frequently of
changes that may affect its compliance
with OFPA or the USDA organic
regulations, e.g., additional crops
produced, inclusion of new land area
and producer group members.
Producer group operations must also
show evidence of compliance with the
USDA organic regulations through
internal inspections and reporting
sanctions imposed on producer group
members. It is not feasible for certifying
agents to inspect each producer member
annually, due to the number of members
in any one producer group operation.
However, the producer member must
attend the internal inspection to provide
complete information about their
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production activities (§ 205.400(g)(8)).
Internal inspections must include massbalance audits and reconciliation of
each producer group member’s and each
producer group production unit’s yield
and group sales. Records are critical to
demonstrate compliance and producer
group operations must maintain a
recordkeeping system so that products
are traceable from producer group
members’ individual production parcel
to aggregation and handling at the
production unit and through sale or
transport when the products leave the
custody and ownership of the producer
group operation (§ 205.400(g)(9)).
Internal Control Systems
Pursuant to the 2002 NOSB
recommendation ‘‘Criteria for
Certification of Grower Groups’’ 50 and
an August 2020 IFOAM position
paper,51 all producer group operations
must have an internal control system
(ICS). The internal control system is an
internal quality management system
that establishes and governs the review,
monitoring, training, and inspection of
the producer group operation, and the
procurement and distribution of shared
production and handling inputs and
resources, to maintain compliance with
the USDA organic regulations. The ICS
consists of both the personnel and the
procedures that form a producer group’s
internal governance, verification, and
enforcement system. The ICS is
responsible for the overall governance
and compliance of the producer group
operation and verifies each member’s
adherence to the organic system plan
and USDA organic regulations.
ICS Functions
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A producer group operation must
have an OSP that meets the
requirements for all operations in
§ 205.201(a) and additionally must
describe its ICS procedures and
practices. Section 205.201(c) describes
the OSP requirements that are specific
to producer group operations. The OSP
for a producer group operation needs to
include a description of the ICS and
how it verifies the operation’s
compliance with the USDA organic
regulations. This includes defining the
organizational structure, roles,
qualifications, and responsibilities of all
ICS personnel (§ 205.201(c)(1)).
50 NOSB Formal Recommendation, Criteria for
Certification of Grower Groups, October 20, 2002:
https://www.ams.usda.gov/sites/default/files/
media/Rec%20Criteria%20for%20Certification
%20of%20Grower%20Groups.pdf.
51 ‘‘Internal Control Systems (ICS) for Group
Certification,’’ IFOAM Organics International,
August 2020, https://www.ifoam.bio/our-work/how/
standards-certification/internal-control.
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Personnel qualifications could include,
for example, knowledge of local
production practices, organic
production and handling practices, ICS
procedures, USDA organic regulations,
and fluency in the language(s) of the
producer group operation.
The ICS must also describe and
prevent conflicts of interest between ICS
personnel and the producer group
operation that it oversees
(§ 205.201(c)(3)). The USDA organic
regulations identify conflict of interest
scenarios for certifying agent and
operations (§ 205.501(a)(11)). The ICS
personnel-producer member
relationship is different than the
certifying agent-certified operation
relationship so these criteria are not
wholly applicable to producer group
operations. For example, certifying
agents are not permitted to consult with
operations to overcome obstacles to
certification. However, ICS personnel
are required to provide training,
education, and resources to assist
producer members with awareness of,
and compliance with, organic
requirements. A generally accepted
criteria for conflict of interest is whether
an oversight entity, e.g., the ICS, has a
financial interest in the regulated party
or likely bias based on familial relations.
For example, internal inspectors should
not inspect family members or
production units where the inspector is
a member.
The oversight function of the ICS
places its personnel at a higher risk for
retribution from producer group
operations. To support the integrity of
ICS oversight, the ICS must also
describe how it will protect ICS
personnel from retaliation for carrying
out their responsibilities, and, in
particular, finding and reporting
noncompliances (§ 205.201(c)(3)). This
could include obtaining a written
guarantee from the producer group
operation that ICS personnel will not be
subject to retribution and requiring ICS
personnel to disclose any conflicts of
interest prior to internal inspections or
review.
The ICS must document and apply
procedures for adding new members to
a producer group operation
(§ 205.201(c)(5)). These procedures must
cover how each new member will be
inspected by the ICS and evaluated to
determine whether they can fully
comply with the organic production and
handling requirements before they are
added as a producer member.
Producer group members use common
practices to produce, harvest, and
handle their collective products and
common inputs. Shared farming or
harvesting practices could include
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3595
fertility and pest management,
procurement of inputs (including seeds
or soil amendments), and shared
resources could include post-harvest
handling facilities. The ICS must
describe how shared resources,
including production practices and
inputs, are procured and provided to all
producer group members and personnel
(§ 205.201(c)(7)). Shared practices and
inputs are critical to fostering
compliance among many individual
farmers and documenting these
practices is an important indicator of
compliance for the entire operation.
Training, education, and technical
assistance are critical practices to
support consistent and compliant
practices among producer members and
the description of the ICS must explain
how these resources are provided
(§ 205.201(c)(8)).
Internal Oversight
The ICS is the first line of oversight
of a producer group operation and is
responsible for assessing the compliance
of producer group members. The USDA
organic regulations include several
requirements to ensure that the ICS
provides competent and thorough
oversight. More generally, the ICS must
have documented clear policies and
procedures to verify the producer group
operation’s and producer group
members’ compliance with the USDA
organic regulations (§ 205.201(c)).
The ICS must identify criteria for
high-risk producer group members and
production units (§ 205.201(c)(6)).
Certifying agents must also determine
which producer members are high risk.
Examples of risk factors that may be
used by both the ICS and the certifying
agent are listed below in the discussion
of on-site inspection by the certifying
agent.
Clear and comprehensive records are
a critical component of an ICS. They
help certifying agents understand how
the operation is implementing its
organic system plan and complying
with the USDA organic regulations. The
organic system plan must describe the
system of records maintained by the ICS
(§ 205.201(c)(9)). The system of records
must show how records will support
and be used for mass-balance
calculations and traceability throughout
the operation. For full traceability,
records would need to cover the
purchase, acquisition, or production of
products for each producer member
through sale or transport.
The description of the ICS must
explain internal monitoring,
surveillance, sanctions, inspection, and
auditing methods used to assess
compliance of all producer group
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members (§ 205.201(c)(10)). As a best
practice, internal monitoring and
surveillance should cover critical
organic control points may include, for
example, buffer areas, condition of
crops and/or wild crops and animals,
soil quality indicators, handling
practices, input and equipment use and
storage areas. A description of sanctions
may cover the review of internal
inspection results to determine member
compliance; and the processes to
address noncompliances, impose
sanctions, remove noncompliant
producer group members and reporting
noncompliances to the certifying agent.
A description of the auditing methods
could cover mass-balance audits to
reconcile the expected and actual yields
and sales of producer members,
producer group production units, and
producer group operations.
On-Site Inspections by the Certifying
Agent
Certifying agents are the second tier of
oversight for producer group operations.
Certifying agents, in addition to
verifying that producer group operations
are fully compliant with the eligibility,
certification and ICS requirements, must
follow specific requirements for on-site
inspections of producer group
operations. Initial and annual on-site
inspections of producer group
operations must comply with the
general requirements for inspections in
§ 205.403. During annual on-site
inspections of producer group
operations, certifying agents are
required to evaluate the ICS, review
internal inspections conducted by the
ICS of individual members, and observe
ICS personnel conducting internal
inspections (§ 205.403(a)(2)(i)–(ii)). At
least one producer group member from
each producer group production unit
must be inspected, and each handling
facility, including all collection sites,
must be inspected (§ 205.403(a)(2)(iii)–
(iv)). Collection sites, where the harvest
from multiple producer group members
is stored before transport, are handling
facilities, and are inspected by certifying
agents. USDA organic regulations do not
set a minimum number or percentage of
witness inspections that a certifying
agent must conduct at each producer
group operation inspection. Witness
inspections are a key component of
assessing the ICS and certifying agents
will need to ensure that the number of
witness inspections at a given operation
is sufficient to evaluate ICS rigor.
During on-site inspections, certifying
agents must inspect at least 1.4 times
the square root or 2% of the total
number of producer group members,
whichever is higher
(§ 205.403(a)(2)(iii)).52 The square root
sampling rate aligns with industry
practice. Two sampling rates are
provided because the power of the
square root sampling power begins to
decline when operations exceed 5,000
members so that a smaller proportion of
members are inspected relative to the
total number of members. The addition
of the 2% rate more evenly distributes
the number of external inspections
across producer groups regardless of the
number of members as shown in Table
1. For each producer group operation,
certifying agents need to calculate the
number of members to inspect using the
square root method and the 2% rate and
use the higher number.
TABLE 1—CERTIFYING AGENT ICS INSPECTION SAMPLING RATES
Producer group members
(N)
Square root
method
Flat 2%
Final rule
N
1.4 * √N
2%
Greater of 1.4 *
√N or 2%
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50 .............................................................................................................................................
100 ...........................................................................................................................................
250 ...........................................................................................................................................
500 ...........................................................................................................................................
1000 .........................................................................................................................................
5000 .........................................................................................................................................
7500 .........................................................................................................................................
10000 .......................................................................................................................................
10
14
23
32
45
99
122
140
1
2
5
10
20
100
150
200
10
14
23
32
45
100
150
200
The number of producer group
members inspected by the certifying
agent must include all high-risk
members (§ 205.403(a)(2)(iii)). Certifying
agents must inspect at least one
producer group member in each
production unit (as defined in § 205.2)
to ensure all producer group production
units are inspected, as well as each
handling facility. As a best practice,
AMS recommends that certifying agents
also select members from across the risk
spectrum—including lower-risk
members—so that the same producer
members are not inspected year after
year. This may require a sample size
larger than the minimum required (i.e.,
more than 1.4 times the square root or
more than 2% of the number of
producer group members). All numbers
must be rounded up to the next whole
number (e.g., using square root method,
50 members = 10 inspections, 100
members = 14 inspections, 500 members
= 31 inspections, and 1,000 members =
44 inspections). The certifying agent has
the discretion to inspect more producer
group members than the minimum
indicated by the calculation.
Risk-based inspections rely upon
certifying agents having policies and
procedures to determine the risk factors
associated with producer group
operations. While the ICS determines
which producer members and
production units are high-risk according
to their criteria, the certifying agent
needs to independently determine
which members are high-risk
(§ 205.403(a)(2)(iii)). The certifying
agent should apply the risk assessment
procedures to determine and instruct
the inspector on which producer group
members to inspect during the annual
inspection. After all risk-based and
other inspection selection criteria are
satisfied, certifying agents should
randomly select the remaining member
inspections so that different lower-risk
producer group members are inspected
each year.
Risk factors may include, but are not
limited to, producer group
administrative capacity, organization
complexity, and variations in members
and production units (such as product
quantity and value, member size,
52 The square root sampling scheme was
developed in the 1920s as a sampling scheme for
agricultural regulatory inspectors. The formula used
was the square root (Sqrt) of the lot size (N) + 1.
Blanck, F.C. (1927). ‘‘Report of the Committee on
Sampling,’’ J. Assoc. Official Agricultural Chemists,
10, 92–98.
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number of products), rate of growth, and
compliance and enforcement history.
For example, a producer group member
selling products outside of the producer
group or a producer group member that
is considerably larger than the other
producer group members in a
production unit represent compliance
risks to the overall producer group
operation. When assessing the risks of
the producer group operation to
determine which producer group
members to inspect, examples of risk
factors that the certifying agent may
consider include, but are not limited to:
• Noncompliance history of overall
producer group and of individual
members;
• The criteria used to designate a
collection of producer group members
as a single producer group production
unit;
• High-risk members identified in the
ICS and producer groups member with
noncompliances;
• Application of prohibited materials
adjacent to member fields;
• Split or parallel operations (i.e.,
operations that are also producing
nonorganic agricultural products);
• Producer group members with
incomes greater than $5,000 USD per
year;
• The procurement, availability, and
distribution of inputs and resources to
members;
• The prevalence of nonorganic
production of similar products and
crops in the region;
• Post-harvest handling practices
designed to prevent commingling and
contact with prohibited substances;
• New producer group members;
• Size of producer group member’s
production or gathering areas; and
• Significant expansion of a producer
group member’s production area.
As a best practice, the inspection of
the ICS should also include: document
review; auditing of production and
sales/distribution records; reconciliation
of product inventory; review of
procurement and distribution of inputs;
review of the inspections conducted by
the ICS; review of ICS personnel
qualifications and training; witness
audits to observe ICS inspectors; review
of noncompliance actions for producer
group members; examination of organic
control points and high-risk areas;
interviews with managers responsible
for the OSP, governance of the ICS, and
producer group members and
individuals overseen by the ICS; and
review of training provided to ICS staff
and producer group members.
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Summary of Changes to Final Rule
AMS made several changes to the
proposed regulatory text when writing
this final rule. Changes to the final rule
are discussed below and are followed by
responses to specific themes from
public comment.
• AMS revised the definitions of
producer group member, producer
group operation, producer group
production unit and internal control
system to allow livestock production
and to clarify that the operation is
regulated as a person. Use of the term
‘‘individual’’ in producer group member
and ‘‘person’’ in producer group
operation more clearly indicates that the
operation is the legal regulated entity,
which is consistent with current
regulation and ties to the existing
defined term person (see § 205.2).
• AMS replaced ‘‘crop/wild-crop’’
with ‘‘agricultural product’’ throughout
so that livestock and livestock products
are not excluded from producer group
operation production. Public
commenters argued that a prohibition
on livestock in producer group
certification may disproportionately
affect poor and small-scale farmers that
depend on producer groups to access
the organic market. Livestock
production in producer group
certification is consistent with EU
organic standards, IFOAM, the 2008
NOSB recommendation, and current
practice in the organic industry.
Allowing livestock production avoids
market disruption and negative impact
to operations that depend on producer
group certification for market access.
• AMS added more specificity to the
description of the ICS in the organic
system plan, including: describing
qualifications of ICS personnel;
procedures for approving new members;
policies to protect ICS personnel from
retribution; description of technical
assistance to members; and a system of
records that covers each member and
support mass-balance audits and
traceability. Public comments stressed
the importance of the ICS and suggested
modifications to strengthen the ICS’s
ability to enforce the organic regulations
and maintain organic integrity. AMS
agrees with public comments and has
revised ICS requirements to be more
specific because this is necessary to
bolster the oversight and enforcement of
producer groups.
• AMS clarified that producer group
operations must only sell products from
the land and facilities included in the
certification. The proposed text only
specified ‘‘from grower group
members.’’ Additionally, requiring that
producer groups only sell products
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3597
produced using land and facilities
within the certified operation improves
oversight because these facilities and
land are routinely inspected by the ICS
and the certifying agent.
• AMS added a requirement that
producer group operations must
maintain an ICS as described in the
organic system plan. Although it was
implied, proposed § 205.400(g) did not
include an explicit requirement to
maintain an ICS and did not reference
the ICS requirements (§ 205.201(c)).
Adding this explicit requirement makes
an ICS a clear condition of certification
that must be included as part of an
organic system plan.
• AMS clarified that producer group
members must be present during
internal inspections. Having producer
group members present during onsite
internal inspections is necessary so that
ICS personnel can interact with and ask
questions of the members to ensure a
full understanding of the activities on
the members’ production sites.
• AMS removed a redundant
requirement from § 205.400(g) that the
producer group operation must
document and report the use of
sanctions; the description and
implementation of a system of sanctions
is covered in §§ 205.201(c)(10) and
205.400(g)(4) and (10).
• AMS adjusted the sampling rates
certifying agents must use when
inspecting producer groups to 1.4 times
the square root or 2% of the total
number of producer group members,
whichever is higher. The proposed
inspection rate of 1.4 times the number
of members is a digressive rate, which
samples a smaller percentage of
members as a group grows larger.
Combining this with a linear 2%
sampling rate ensures that larger
producer groups (those with more than
5,000 members) are inspected at a
similar rate as smaller groups.
• AMS revised § 205.403(a)(2)(iii) to
clarify that a certifying agent must
inspect all producer group members
determined to be high-risk by the
certifying agent. The proposed rule had
stated that high-risk members should be
chosen based on the ICS’s risk criteria.
This change improves oversight by
ensuring that a certifying agent conducts
independent risk assessments based on
their own risk criteria, rather than
relying only on the ICS’s assessment.
Summary of Public Comments
The majority of public comments
received supported AMS’s codification
of producer group standards in the
USDA organic regulations. Many
comments provided suggestions and
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recommendations to the proposed
policy.
Many comments strongly opposed the
proposed prohibition of livestock
production within producer groups,
requesting that AMS revise the standard
to allow ‘‘scope neutrality’’ and the
production of livestock and livestock
products. Several commenters stated
that many certified producer groups
already produce livestock and livestock
products, and that prohibiting livestock
would negatively impact these
operations.
Several comments suggested AMS
add more specificity to the proposed
ICS requirements to ensure the ICS can
manage the unique challenges of
producer groups. Commenters requested
more detail about conflict of interest,
training, risk assessment, inspections,
recordkeeping, personnel qualifications,
protections for farmers, and evaluation
of the ICS by the certifying agent.
Commenters pointed to specific details
found in the preamble describing
organic system plans and the internal
control system and requested these be
added to the final rule to support clarity
and consistency.
The proposed rule asked if producer
group risk should be managed by
placing limits on scale (e.g., number of
members, size of individual members,
geographic distribution of members).
Most commenters agreed that the risks
of uncontrolled size or scale should be
addressed but felt prescriptive limits
may arbitrarily exclude members,
disrupt well-functioning groups, restrict
economic opportunity, or force
producers to revert to conventional
methods. The majority of commenters
advocated for ‘‘scale neutrality’’ and
requested NOP develop alternate
strategies to manage the risks of large
producer group operations.
Several comments requested that
AMS require the use of risk criteria and
assessment to control issues of scale.
Others recommended that AMS develop
a separate scope of accreditation
specifically for producer groups, arguing
that certification of these operations
requires specialized skill and oversight.
A few comments noted the difficultly of
identifying producer groups in the
Organic Integrity Database, and asked
for identification to be mandatory. Some
comments noted differences between
the proposed policy and other
international standards, and asked AMS
to align its producer group standards
with EU and IFOAM. Finally, a few
comments expressed concern that the
producer group standard may be used
by large livestock or poultry
cooperatives in the United States, which
they argue is against the intent of the
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standard to support opportunity and
growth for very small organic farmers.
Responses to Public Comments
(Comment) Some commenters
recommended specific limits on parcel
size and number of members in a
producer group operation because a lack
of controls on scale could lead to
inadequate and inconsistent
enforcement. Commenters mentioned
that an ICS could be reluctant to enforce
against a large producer member
without which the producer group
could fail.
(Response) AMS is not setting size
limitations, in terms of land area or
number of members, on producer group
operations. The ICS requirements
support effective oversight of producer
group operations regardless of their size.
(Comment) Comments opposed the
proposed prohibition of livestock
producer group operations. Commenters
argued that this may disproportionately
affect poor and small-scale farmers that
depend on producer groups to access
the organic market. Some comments
mentioned that livestock producer
group operations are already certified
for beef and honey production.
(Response) AMS revised the proposed
rule to allow the certification of
livestock production as producer group
operations. This allowance aligns with
the EU organic standards for producer
group operations and the 2008 NOSB
recommendation, which did not restrict
producer group certification to crop and
wild crop operations. Livestock
producer group operations may be more
complex and higher risk than crop and
wild crop producer group operations. In
practice, this will require careful
oversight of the ICS and qualifications
of ICS inspectors and personnel.
Further, some types of livestock
production may be unsuitable for group
certification (e.g., intensive livestock
farming, variability between producer
members) because it is more difficult for
them to meet the requirements for
certification as a producer group
operation.
(Comment) Comments requested a
separate scope of accreditation for
producer group certification to ensure
that certifying agents are sufficiently
qualified to certify producer groups.
(Response) Establishing a separate
scope of accreditation would require
more input and assessment of impacts,
as this was not included in the proposed
rule. This type of certification is
complex and presents higher risks for
organic integrity. AMS will assess
certifying agents’ oversight of and
qualifications for producer group
certification through rigorous audits.
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(Comment) Comments suggested that
the ICS should describe the
qualifications of all ICS personnel and
the procedure to ensure the availability
of a sufficient number of qualified
personnel. Comments specified that the
ICS should describe how ICS personnel
are familiar with the local production
practices, general organic production
and handling practices, the USDA
organic regulations, ICS procedures and
regulations, and be fluent in the
language(s) of the producer group
members and the ICS.
(Response) The description of the ICS
must describe the qualifications and
responsibilities of ICS personnel. AMS
has identified examples of the
knowledge qualifications for ICS
personnel, but is not adding these as
required to give flexibility to certifying
agents to determine the suitable
qualifications on specific operations.
(Comment) Comments asserted that
producer group operations must ensure
that all group members understand and
can comply with the USDA organic
regulations. Commenters urged that the
ICS should describe how the training,
education, and technical assistance that
is provided to producer group members
and ICS personnel ensures their
understanding of and compliance with
internal control system’s policies, the
organic system plan, and the USDA
organic regulations.
(Response) Producer group operation
compliance requires that each member
understand the required and prohibited
practices for organic production and
handling. AMS has added a requirement
for the ICS to include training,
education, and technical assistance to
producer members (205.201(c)(8)).
Given that producer group operations
are located in areas with varying
language and literacy proficiency, it is
the responsibility of the operation to
effectively communicate this
information to all members on an
ongoing basis.
(Comment) Comments stated that the
ICS should explain how it manages
conflicts of interest by addressing or
prohibiting internal inspectors from
inspecting or acting as buying officers
for their own relatives. Comments also
requested guidance around conflict-ofinterest scenarios and that internal
inspectors are not restricted from
providing training, education, or
technical assistance to producer group
members.
(Response) The description of the ICS
must explain how it will prevent
potential conflicts of interest. The
development of guidance on specific
examples of conflict of interest needs
further public input and discussion and
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that level of detail was not included in
the scope of this rule. Certifying agents
will review the ICS to determine if
known potential conflicts of interest are
identified and prevented. AMS agrees
that internal inspectors inspecting or
procuring products from their relatives
would be potential conflicts of interest
because the relationship may
compromise the inspector’s objectivity
in assessing compliance.
(Comment) Comments stressed that
group members need to be present
during their internal inspection and that
more guidance is needed to ensure the
ICS is addressing noncompliances and
reporting major noncompliances to the
certifying agent.
(Response) AMS has added the
requirement for producer members to be
present at the inspection of their
production site(s). Maintaining an
organized, transparent, and equitable
system of sanctions is critical for
producer group certification. The ICS
must have procedures for implementing
a system of sanctions, and the producer
group operation must report sanctions
for noncompliant members to the
certifying agent. The requirements for
recordkeeping that covers internal
inspection reports, sanctions, and
corrective actions plus the external
inspection requirements will help
certifying agents to assess whether the
ICS is reporting noncompliances and
sanctions to the certifying agent.
(Comment) Comments supported that
the ICS describe the recordkeeping
system that must cover signed member
agreements, internal inspection reports,
documents related to internal sanctions
and corrections, and formal agreements
for each producer group member that
commits them to complying with ICS,
OSP, and USDA organic regulations,
along with all training records for
members and personnel. The ICS
procedures should state how lists of
individual members, locations,
products, acreage, copies of inspection
reports, sanctions, and corrections are
stored and made available during
inspection by the certifying agent.
(Response) The USDA organic
regulations require a description and
implementation of the recordkeeping
system. The critical objective of
recordkeeping is to support traceability
of production, inputs, and transactions
throughout the producer group
operation. Information about sanctions
and internal inspection reports are
required by separate provisions.
(Comment) Comments requested
clarification about what types of
noncompliances (i.e., major vs minor)
must be reported to the certifying agent.
(Response) The requirement to report
noncompliances to the certifying agent
enables the certifying agent to assess ICS
oversight. It also leaves flexibility for
the ICS to describe different timing and
reporting methods for noncompliances
of varying scope and severity.
Noncompliances that may result in
removal of the member(s) from the
producer group, for example,
application of prohibited substances,
warrant timely notification to the
certifying agent. In contrast, maintaining
records of correctable noncompliances
for the certifying agent to review during
external inspections would be
acceptable.
(Comment) Comments stated that the
use of 1.4 times the square root of the
number of members is not adequate for
external inspections. They explained
that this inspection rate is either too low
for a producer group with more than
Section
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205.302 ...............................
5,000 members, resulting in potentially
inadequate oversight of very large
groups, or the inspection rate is too high
and burdensome for small producers,
resulting in pressure to grow larger to
reduce certification costs. Comments
suggested other rates including a flat
percentage rate of 2–3%, a combination
of square root and flat rate methods, or
a minimum of 10% of producer group
members.
(Response) The external inspection
sampling rate should be equally
stringent for producer member
operations regardless of size. The USDA
organic regulations specify that
certifying agents must use the higher
result of 2 sampling rates to set the
minimum number of producer members
that need to be inspected. Setting 2 rates
is necessary because the square root
sampling power begins to decline when
producer groups are larger than 5,000
members. The use of 1.4 times the
square root or 2% of the total number
of producer members is a minimum and
does not prevent certifying agents from
using sampling sizes that exceed the
results of those rates. Higher levels of
inspection rates may be warranted when
necessary if a producer group operation
has a history of inadequate internal
controls and poorly trained personnel
with ineffective policies, procedures, or
sanctions, and is failing to enforce
against noncompliant members, failing
to inspect all members, or is not
completing mass-balance audits.
O. Calculating the Percentage of
Organically Produced Ingredients
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Calculating the percentage of organically produced ingredients.
Paragraphs (a)(1), (2), and (3).
This rulemaking revises § 205.302(a)
to clarify that the percentage of organic
ingredients in multi-ingredient products
should be calculated by dividing the
weight or volume of the organic
ingredients at formulation by the total
weight or volume of the product at
formulation, with water and salt added
as ingredients at formulation excluded
from the calculation.
This policy may affect certified
operations, noncertified operations that
process products containing organic
ingredients, applicants for organic
certification, and certifying agents. The
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reader should carefully examine the
regulatory text and discussion below.
Background
Section 205.301 of the organic
regulations classify products containing
organic ingredients into several
categories based on percent
composition—e.g., ‘‘100 percent
organic,’’ ‘‘organic,’’ ‘‘made with organic
(specified ingredients or food
group(s)).’’ Clear and easily understood
instructions for calculating product
composition are needed to ensure
consistent classification by the organic
industry.
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Previous policy had sometimes
caused inconsistent implementation
because it required calculation based on
‘‘total weight of the finished product.’’
It was unclear if this meant products
before or after processing. Because
processing (e.g., cooking, baking,
dehydrating, freeze drying) often causes
water loss from ingredients, using the
total weight of the product after
processing sometimes resulted in
inflated percent organic content
calculations. This rulemaking clarifies
that organic content must be calculated
from the weight of ingredients at
formulation (i.e., before processing such
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as baking or cooking). This will ensure
correct calculation of organic content so
that labels on multi-ingredient organic
products are accurately listed. This
requirement also addresses an existing
point of confusion and will increase the
consistency of organic labeling claims in
processed organic products. This policy
is consistent with both an April 2013
NOSB recommendation 53 and NOP
5037 Draft Guidance published by AMS
in December 2016.54
Calculating Percentage of Organic
Ingredients
To calculate the percentage of organic
ingredients in a multi-ingredient
product, divide the weight or volume of
the organic ingredients at formulation
by the total weight or volume of the
product at formulation. If water and salt
are added as ingredients, these must be
excluded from the calculation. If a
multi-ingredient product contains only
liquids, volume must be used for
calculation. If a product contains both
solid and liquid ingredients, weight
must be used for calculation. Please see
Table 2, below, for an example of how
to calculate the percentage organic
content of a multi-ingredient product.
Liquid ingredients being reconstituted
from concentrates should be calculated
based on single-strength concentrations.
The term ‘‘single-strength’’ is defined by
the Food and Drug Administration (21
CFR 101) as equivalent to the Brix value
of 100 percent juice. Brix is a
measurement referring to the percent, by
mass, of soluble solids (generally sugar)
in a solution. Brix is a useful reference
in identifying single-strength identities
of juices (see 21 CFR 101.30(h)(1)) as the
mass of sugar and other soluble solids
is not affected by the concentration
process (i.e., the same mass of sugar will
be present in 1 liter of apple juice
measured at 11.5 Brix, as is present in
0.5 liters of concentrated apple juice
measured at 23 Brix). Reconstitution is
taking a concentrated juice product and
adding water to dilute the concentrated
juice back to single-strength values.
Using the previous example, if a
producer starts with 0.5 liters of
concentrated apple juice, they could
add water to increase the total volume
to 1 liter, bringing the juice back to the
original Brix value of 11.5. Allowing for
reconstituting concentrated juice gives
producers flexibility in shipping,
storage, and use of juice products in
organic production.
For products that have ingredients
composed of multiple ingredients (also
referred to as ‘‘multi-ingredient
ingredients’’), the exact organic content
should be obtained of that multiingredient ingredient when calculating
the total organic content of the final
organic product. In this case, the
calculation should identify the organic
and nonorganic parts of the multiingredient ingredient and supporting
documentation should be available for
the certifying agent to review.
Alternatively, these ingredients should
be calculated as contributing either 95%
organic content or 70% organic content
depending on how the product is
classified (i.e., either ‘‘organic’’ or
‘‘made with organic (specified
ingredients or food groups)’’
respectively).
TABLE 2—CALCULATING PERCENT ORGANIC OF A SOY BEVERAGE
Weight of
ingredient at
formulation
(lbs.)
Ingredient
Organic Soy Base ..................................................................................................
Organic Cane Sugar ..............................................................................................
Organic Vanilla Extract ..........................................................................................
Vitamins .................................................................................................................
Calcium Phosphate ................................................................................................
Carrageenan ..........................................................................................................
Added Water ..........................................................................................................
Added Salt .............................................................................................................
1,100
5,288
60
50
100
100
10,000
5
Total weight (excluding added salt and water) ..............................................
6,698
Total % Organic ..............................................................................................
..........................
Summary of Changes to the Final Rule
AMS replaced the parenthetical
statements ‘‘(excluding water and salt)’’
with the single statement ‘‘Water and
salt added as ingredients at formulation
are excluded from the calculation.’’ This
more clearly states NOP’s intent and
will result in more consistent
calculation of organic content across the
industry.
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Summary of Public Comment
In general, almost all public
comments supported AMS’s
clarification that percent organic
53 NOSB Recommendation, Calculating
Percentage Organic in Multi-Ingredient Products,
April 11, 2013: https://www.ams.usda.gov/sites/
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% Organic
content of
ingredient
% In
formulation
Actual
organic
%
100
100
95
0
0
0
16.42
78.94
0.89
0.74
1.49
1.49
16.4200
78.9400
0.8455
0.0000
0.0000
0.0000
....................
........................
96.2055
content must be calculated based on
weights/volumes at formulation.
However, many comments noted that
the proposed text could be interpreted
to mean that salt and water must be
excluded from each ingredient during
calculation. Commenters explained this
would be difficult and unnecessary to
calculate the amount of water and salt
in some ingredients and asked that AMS
revise § 205.302(a) to state that only
water and salt added as ingredients
should be excluded from calculation.
However, several comments also asked
AMS to clarify that water and salt added
to individual ingredients (e.g., broth or
tea) should be excluded from
calculation.
default/files/media/NOP%20CACC%20
Final%20Rec%20Calculating%20Percentage.pdf.
54 The draft guidance and comments can be
viewed at https://www.regulations.gov/
document?D=AMS-NOP-16-0085-0001 and in the
NOP Program Handbook: https://
www.ams.usda.gov/sites/default/files/media/
NOP5037DraftGuidancePercentCalculations.pdf.
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Responses to Public Comment
(Comment) Many comments noted
that the proposed text could be
interpreted to mean that salt and water
must be excluded from individual
ingredients during calculation.
Commenters explained this would be
difficult and unnecessary to calculate
the amount of water and salt in some
ingredients, and asked that AMS revise
§ 205.302(a) to state that only water and
salt added as ingredients should be
excluded from calculation.
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(Response) AMS has replaced the
parenthetical statements ‘‘(excluding
water and salt)’’ with the single
statement ‘‘Water and salt added as
ingredients at formulation are excluded
from the calculation.’’ This clearly states
that only water and salt added as
ingredients are excluded from
calculation.
(Comment) Several comments asked
NOP to clarify how to calculate
percentage organic content when
ingredients are composed of more than
one ingredient (a ‘‘multi-ingredient
ingredient’’).
(Response) The exact organic content
of a multi-ingredient ingredient should
be used when calculating the total
Section
205.2 ...................................
205.103 ...............................
205.201 ...............................
205.501 ...............................
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205.504 ...............................
organic content of the final organic
product.
P. Supply Chain Traceability and
Organic Fraud Prevention
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Final regulatory text
Terms defined.
Definitions for Organic fraud and Supply chain traceability.
Recordkeeping by certified operations.
Paragraphs (b)(2), and (3).
Organic production and handling system plan.
Paragraph (a)(3).
General requirements for accreditation.
Paragraphs (a)(10), (13), and (21).
Evidence of expertise and ability.
Paragraphs (b)(4) and (7).
Traceability and fraud prevention are
essential in complex organic supply
chains. Because protecting and verifying
organic integrity is a responsibility
shared by many participants in the
organic industry, this rulemaking
requires certified operations and
certifying agents to incorporate supply
chain traceability and organic fraud
prevention into their practices. These
actions will strengthen organic integrity
and reinforce trust in the USDA organic
label.
Certified organic operations must:
• Maintain records of their activities
that span the time of purchase or
acquisition, through production, to sale
or transport;
• Maintain records that trace back to
the last certified operations in their
supply chain;
• Maintain audit trail documentation
to facilitate supply chain traceability,
including identification of agricultural
products as organic on audit trail
documents; and
• Describe in their organic system
plan the monitoring practices and
procedures used to prevent organic
fraud and verify suppliers and organic
product status.
Certifying agents must:
• Conduct risk-based supply chain
traceability audits of products they
certify to verify compliance;
• Maintain procedures for identifying
high-risk operations and agricultural
products, conducting risk-based supply
chain audits, and reporting credible
evidence of organic fraud to the USDA;
and
• Share information with other
certifying agents to conduct
investigations, conduct supply chain
traceability audits, and verify
compliance of organic products.
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These requirements may affect
certified organic operations, certifying
agents, and operations applying for
organic certification. Organic
stakeholders should carefully examine
the regulatory text and policy
discussion below.
Background
Because organic products are
credence goods, the organic system
relies upon on trust between entities in
organic supply chains.55 Therefore,
traceability and verification of organic
products are essential to the function of
a healthy organic market. This is
especially true of modern organic
supply chains, which have grown longer
and more complex. Organic products
and ingredients are often handled by
dozens of operations, including
uncertified entities, on their way to the
consumer. A robust system of
traceability and fraud prevention can
help reduce the risks of complex supply
chains and minimize fraud.
The length and complexity of modern
supply chains present many risks to
organic integrity. Activities that can
compromise organic integrity and void
the use of the USDA organic label
include physical risks such as contact
with substances prohibited in organic
production (e.g., pesticides, fumigants,
or cleaning agents) and mixing or
commingling of organic and nonorganic
products. Integrity can also be
compromised if a nonorganic product is
mistakenly labeled or identified as
organic, or if poor recordkeeping cannot
demonstrate that a product was
produced on a certified farm and
55 A credence good is something with value or
qualities that cannot be easily determined by the
consumer before, or even after, purchase.
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handled according to the organic
regulations. Additionally, fraud can
occur through falsification of records
and labeling to claim that a nonorganic
product is certified organic. Breach of
integrity can occur at any point in a
supply chain, from production to final
sale. In addition, the prevalence in
organic supply chains of uncertified
operations, who do not have direct
USDA or certifying agent oversight,
increases the chance that loss of
integrity may occur and/or go
unreported.
Organic products therefore require
additional care to verify organic status
and ensure that products bought and
sold are genuinely organic and have not
been compromised. Because full
visibility across an entire supply chain
is difficult, this rule focuses on using
critical information at control points
where risk is highest to verify chain of
custody and confirm organic integrity.
This is primarily done by building a
record of product transaction and
movement that demonstrates proper
handling and maintenance of integrity.
Without a verified transaction record,
operations (and by extension,
consumers) don’t have a full picture of
a product’s history, and breaches of
integrity can go unnoticed, allowing
compromised product to continue along
a supply chain to the consumer.
The current USDA organic regulations
require general recordkeeping and
verification of organic integrity, but the
requirements are not specific and lack
key types of information and practices
that are necessary to prove the integrity
of products from long, complex supply
chains. This lack of recordkeeping
information often leads to incomplete
audit trails, and operations and
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certifying agents are often unable to
verify product origin or organic
integrity. The specific recordkeeping,
auditing, and fraud prevention
procedures in this rule will augment
existing practice to ensure more
complete visibility into organic supply
chains. This visibility will allow
operations and certifying agents to
complete more rigorous verification of
organic products and identify and stop
loss of organic integrity before it moves
further into organic supply chains.
All successful systems of traceability
include three common elements: (1)
traceability within a single operation;
(2) traceability one step forward and one
step back from an operation in a supply
chain; and (3) bidirectional traceability
along a supply chain by a third party.
This rulemaking supports traceability by
clarifying who is responsible for each
element: certified organic operations are
responsible for traceability within their
operation, back to their suppliers, and
forward to their customers; certifying
agents are responsible for verifying and
tracing products along a supply chain
and assessing a certified operation’s
system of traceability.
Fraud is also a significant risk to
organic integrity; this rulemaking
therefore focuses effort on its
prevention. To clarify what this means,
§ 205.2 of the organic regulations
includes a definition of organic fraud:
deceptive representation, sale, or
labeling of nonorganic products as ‘‘100
percent organic,’’ ‘‘organic,’’ or ‘‘made
with organic (specified ingredients or
food group(s)).’’ This broad definition
helps clarify portions of this
rulemaking’s policy (e.g.,
§§ 205.201(a)(3) and 205.504(b)(7)), but
is not intended to be used as a
mechanism or criterion for enforcement.
Certified Operations
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Recordkeeping
Section 205.103 of the organic
regulations describes the recordkeeping
responsibilities of certified operations.
Records are used by operations,
certifying agents, the USDA, and others
to verify the compliance of organic
operations and products. Clear and
auditable records also support
traceability. This rulemaking clarifies
recordkeeping requirements to support
the traceability of organic products both
within and between operations.
General Recordkeeping Requirements
Section 205.103(b)(2) specifies that a
certified operation’s records must
describe all activities and transactions
of the operation. This includes physical
and financial possession, production,
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handling, title, and contractual
oversight responsibilities of the organic
products and ingredients the operation
produces or handles. Such records must
span the time of purchase or
acquisition, through production, to sale
or transport. This requirement supports
‘‘internal’’ traceability, or the ability to
track the movement, handling, and
organic status of products within a
single operation. These records are
needed to verify the compliance of an
organic operation and its products, and
supports on-site inspections by
providing information for mass-balance
audits and traceability verification by
certifying agents (see § 205.403(d)(4)–
(5)).
Section 205.103(b)(2) also requires
that an operation’s records must be
sufficient to trace products back through
a supply chain to the last certified
operation. Keeping ‘‘external’’ records
back to the last certified operation is
needed to verify the source of organic
products. Note that records must reach
back to the last certified operation.
Operations receiving organic products
from uncertified suppliers (e.g., an
exempt wholesaler) must keep records
demonstrating how the uncertified
operation maintained organic product
integrity. This may require keeping
records from several uncertified
operations in sequence; in all cases the
records must show an audit trail back to
the last certified operation. Operations
can demonstrate an audit trail by using
various types of documentation that are
typically used during sale, purchase,
and transfer, such as receipts, invoices,
shipping or receiving manifests,
shipping logs, bills of lading, or
transaction certificates. The organic
industry creates and transfers this
documentation (almost always
electronically) in the usual course of
business, and sales contracts often list
this documentation as a condition of the
sale. Typically, handling entities along
a supply chain (such as a transporter,
broker, or storage facility) will send
electronic documentation directly to the
buyer either before or at receipt of a
product. A buyer may also obtain
additional documents or records
directly from the certified operation that
sold the product.
Maintaining records back to the last
certified operation will support supplier
verification and fraud prevention plans
(§ 205.201(a)(3)). Such records will also
ensure certifying agents have the
information they need to verify the
compliance of products during on-site
inspections (§ 205.403(d)(5)) and during
supply chain traceability audits
(§ 205.501(a)(21)).
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Section 205.103(b)(2) describes a
certified operation’s minimum
recordkeeping requirements. Certified
operations may need to keep additional
records beyond the scope of
§ 205.103(b)(2) to comply with other
portions of the organic regulations and
the Act. For example, to comply with
§ 205.236, Origin of livestock, livestock
operations must maintain records
demonstrating that animals were
organically managed from the last third
of gestation, which may include place
and date of birth. This may require
records that trace purchased animals
back to the operation where the animal
was born to prove origin and organic
management (i.e., the records must trace
beyond the last certified operation to
prove compliance).
Audit Trail Documentation
Certified operations must keep audit
trail documentation for all organic
products they produce or handle. Audit
trail documents are records used to
determine the source, transfer of
ownership, and transportation of
organic products (see definition of audit
trail in § 205.2). For the purpose of audit
trail documentation, the ‘‘source’’ of
organic products is the certified
operation that supplied the product to
the operation. Examples of audit trail
documentation may include but are not
limited to receipts, invoices, shipping or
receiving manifests, shipping logs, bills
of lading, and transaction certificates.
Audit trails must document the history
of organic products back to the last
certified operation (per § 205.103(b)(2)).
Audit trail documentation must
identify organic products as ‘‘100%
organic,’’ ‘‘organic,’’ or ‘‘made with
organic (specified ingredients or food
group(s)),’’ as appropriate. Operations
may use abbreviations or acronyms to
identify products, provided that the
abbreviations or acronyms are easily
understood. Certified operations should
consider describing use of any
abbreviations or acronyms in their OSP;
this will facilitate on-site inspections
and record audits by certifying agents,
and help ensure that records are
‘‘readily understood and audited’’
(§ 205.103(b)(2)).
Explicit identification of products as
organic is required for audit trail records
(i.e., ‘‘transaction’’ or ‘‘external’’
records). ‘‘Internal’’ records do not need
to provide explicit organic identification
(e.g., ‘‘100 percent organic’’). However,
all systems of records must be ‘‘in
sufficient detail as to be readily
understood and audited’’ to meet the
requirements of § 205.103(b)(2). This
means that operations must be able to
identify products they produce or
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handle as organic, even if records do not
explicitly state ‘‘organic.’’ For example,
an operation may use an inventory
management system that uses lot codes,
batch numbers, or other designation
system that indicates organic status.
Such designation systems must be clear
and auditable to facilitate on-site
inspection and verification of
compliance.
Audit trail documentation that clearly
identifies organic products will support
an operation’s verification of suppliers
and implementation of fraud prevention
plans. They will also allow certifying
agents to verify compliance of suppliers
and products during on-site inspections
(§ 205.403(d)(5)) and supply chain
traceability audits (§ 205.501(a)(21)).
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Fraud Prevention Plans
Section 205.201(a)(3) requires all
certified operations to maintain and
implement practices to verify the
organic status of suppliers and products
in their supply chain and to prevent
organic fraud. Often called ‘‘fraud
prevention plans,’’ these procedures and
practices support early detection,
prevention, and mitigation of fraud, and
strengthen integrity across organic
supply chains.
A fraud prevention plan must be
included in an operation’s OSP. This
allows certifying agents to assess the
effectiveness of certified operations’
anti-fraud practices and compliance
with the organic regulations. A fraud
prevention plan must be appropriate to
the activities, scope, and complexity of
the operation, and should be sufficient
to address the verification and antifraud needs of the particular operation.
This means not all fraud prevention
plans will be alike. For example, a
producer who does not handle another
operation’s organic products may
develop a simple fraud prevention that
verifies purchased inputs comply with
organic regulation. In contrast, a
processor that receives many organic
ingredients from numerous suppliers
should develop a fraud prevention plan
that describes practices to detect,
prevent, minimize, and mitigate organic
fraud risks in lengthy supply chains.
Because fraud prevention plans must
verify the organic status of suppliers
and organic products, they should
include a description of how an
operation verifies organic status back to
the last certified operation in the supply
chain. This supports recordkeeping and
audit trail requirements at
§ 205.103(b)(2) and (3) and allows
certifying agents to verify compliance
during on-site inspections and supply
chain traceability audits.
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As a best practice, a robust plan for
supply chain oversight and organic
fraud prevention may include:
• A map or inventory of the
operation’s supply chain that identifies
suppliers;
• Identification of critical control
points in the supply chain where
organic fraud or loss of organic status
are most likely to occur;
• A vulnerability assessment to
identify weaknesses in the operation’s
practices and supply chain;
• Practices for verifying the organic
status of any product they acquire and/
or use;
• A process to verify suppliers and
minimize supplier risk to organic
integrity;
• Mitigation measures to correct
vulnerabilities and minimize risks;
• Monitoring practices and
verification tools to assess the
effectiveness of mitigation measures;
and
• A process for reporting suspected
organic fraud to certifying agents and
the NOP.
conduct SCT audits. SCT audits
conducted by the certifying agent must
be based on these criteria and
procedures. To ensure that AMS is
made aware of organic fraud when it is
discovered, certifying agents must also
maintain procedures to report credible
evidence of fraud to the USDA. Copies
of these procedures and criteria should
be kept by the certifying agent to
demonstrate its expertise and ability
(§ 205.504(b)(7)); this allows AMS to
review and evaluate use of SCT audits
during regular accreditation audits.
SCT audits should be initiated by
events or criteria chosen and described
by the certifying agent. For example,
SCT audits may be initiated to
investigate evidence or suspicion of
fraud, verify compliance of an organic
product, investigate patterns of activity,
trace the source of positive residue
testing, surveil high-risk supply chains
or products, or to address any other
compliance-related risk, activity, or
need identified by the certifying agent.
Certifying Agents
The length, extent, and frequency of
an SCT audit may vary and should be
determined by the objective of the audit
(i.e., an SCT audit ends when its
objective is achieved). SCT audits may
trace back to the origin (production site)
of a product, or until a noncompliance
is verified or cleared. For example, if a
certifying agent’s objective is to verify
the production origin of an ingredient,
the SCT audit should trace the
ingredient through the entire supply
chain to the farm or ranch where the
ingredient was produced. In contrast, if
an SCT audit is initiated to determine
the source of a positive residue test, the
SCT audit may conclude when the
source of the contamination is identified
(which may only be several ‘‘steps’’
back in the supply chain).
The number, frequency, type, and
extent of SCT audits should be
appropriate to the number, scope, and
complexity of operations the certifying
agent certifies.
Supply Chain Traceability Audits
Traceability of organic products
across multiple operations in a supply
chain is an effective strategy to detect
fraud, conduct investigations, and verify
compliance of products and operations.
Therefore, § 205.501(a)(21) of the
organic regulations requires certifying
agents to conduct risk-based supply
chain traceability audits of products and
operations they certify.
What is a supply chain traceability
audit?
A supply chain traceability audit
(SCT audit) is the process of identifying
and tracking the movement, sale,
custody, handling, and organic status of
a product along a supply chain. The
objective of a supply chain audit is to
verify a product’s compliance with the
organic regulations. SCT audits can be
used to investigate evidence or
suspicion of fraud, verify compliance of
high-risk products, investigate patterns
of activity, trace the source of products
contaminated with prohibited
substances, surveil high-risk supply
chains, or for other compliance-related
reasons.
Criteria and Procedures for Supply
Chain Traceability Audits
Certifying agents must maintain
criteria and procedures that describe the
use of risk-based SCT audits. This must
include (1) criteria used to identify
high-risk operations and products for
SCT audits, and (2) procedures used to
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Use of Supply Chain Traceability Audits
Information Sharing
To facilitate supply chain traceability
audits, investigations, and verification
of organic status, AMS requires
certifying agents share compliance- and
enforcement-related information with
each other. Per § 205.501(a)(10),
certifying agents must maintain strict
confidentiality with respect to its clients
and not disclose business-related
information to third parties that are not
involved in the regulation or
certification of operations, as required
by the OFPA (7 U.S.C. 6515(f)).
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Certifying agents must exchange
information that is credibly needed to
determine an operation’s compliance
with the USDA organic regulations,
including assessment of applications for
certification, noncompliance
investigations, suspension/revocation of
certification, supply chain traceability
audits, verification of audit trail
documentation, and verification of the
organic status of products represented
as organic (see § 205.501(a)(10)(ii) and
(a)(13)).
Section 205.501(a)(10)(iii) requires
that compliance-related proprietary
business information exchanged
between certifying agents must remain
proprietary, and that all certifying
agents involved in the exchange must
preserve the confidentiality of the
information during and after the
exchange. Certifying agents must
maintain copies of the procedures used
to exchange information and maintain
confidentiality of information
(§ 205.504(b)(4)). These requirements
will ensure confidentiality of
information during compliance
activities that span multiple certified
operations and certifying agents, such as
supply chain traceability audits and
investigations.
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Conclusion
The traceability and fraud prevention
requirements discussed above are part
of a holistic organic control system that
enhances the oversight, enforcement,
and integrity of organic products. Many
other sections of this rule support and
facilitate traceability and fraud
prevention; stakeholders should read
the following sections to better
understand how to implement this
rule’s traceability and fraud prevention
requirements:
• Section III. A: Applicability and
Exemptions from Certification;
• Section III. B: Imports to the United
States;
• Section III. C: Labeling of Nonretail
Containers;
• Section III. D: On-Site Inspections;
• Section III. G: Paperwork
Submissions to the Administrator; and
• Section III. H: Personnel Training
and Qualifications.
Summary of Changes to the Final Rule
AMS made several changes to the
proposed regulatory text when writing
this final rule. Changes to the proposed
rule are discussed below and are
followed by responses to specific
themes from public comment:
• AMS revised the definition of
organic fraud to remove ‘‘intentional’’
and ‘‘for illicit economic gain.’’
‘‘Intentional’’ is not needed because this
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defined term is not used for
enforcement; it is used to help explain
the objective of this rulemaking and
many of its provisions. AMS removed
the phrase ‘‘for illicit economic gain’’
because not all fraud results in or is
motivated by economic gain. The final
defined term is more flexible than
proposed and encompasses a broader
range of potential fraud types.
• AMS added the new term supply
chain traceability audit. A similar
definition was used in the preamble of
the proposed rule to help stakeholders
understand the rule and its objectives.
AMS added this new term to more
formally clarify its purpose and
objective, and to more clearly define the
expectations of traceability audits by
certifying agents (see § 205.501(a)(21)).
• AMS removed the requirement in
§ 205.103(b)(2) to identify specific
labeling categories (e.g., ‘‘100%
organic’’) in records. Removing this
requirement avoids the potential for
additional recordkeeping burden that
some comments noted the proposed rule
could unintentionally create, and gives
operations more flexibility in how they
keep records.
• AMS specified the scope of
recordkeeping in § 205.103(b)(2) to more
clearly indicate the types of records that
operations should keep, and what
timeframe they should span. This
presents clear expectations that support
traceability and verification of organic
products, but also puts clear boundaries
on the scope of records to control
burden and cost to operations.
• AMS added a requirement to
identify organic status (e.g., ‘‘100
organic’’) in audit trail documentation at
§ 205.103(b)(3) and added ‘‘or similar
terms, as applicable.’’ The proposed rule
had included this at (b)(2) as a general
requirement for all records; the
rulemaking only requires such
identification on audit trail
documentation (see audit trail at
§ 205.2). This change will avoid the
potential for additional recordkeeping
burden that some comments noted the
proposed rule could unintentionally
create, but still ensures that this critical
information is available to trace organic
products between operations and to
verify integrity.
• AMS revised § 205.201(a)(3) to
clarify that fraud prevention plans must
be appropriate to an operation’s
activities, scope, and complexity. This
change responds to public comments
that were concerned about
disproportionate burden (i.e., greater
cost) on small operations, especially
small producers. This change may allow
operations with less complex activities
and/or a more limited scope to write
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and implement simpler fraud
prevention plans.
• AMS removed ‘‘back to the source’’
in § 205.501(a)(21) because public
comments indicated this phrase was
unclear and that the length of supply
chain traceability audits varies. The new
term supply chain traceability audit
states the objective of such an audit—to
verify an organic product’s
compliance—and therefore serves to
clarify that the length and extent of
supply chain traceability audits will
vary depending on the objective and
findings of the process.
• In § 205.501(a)(15), AMS added
references to § 205.504(b)(7) and
§ 205.501(a)(13). This more clearly
specifies that certifying agents are to use
their own criteria for identifying highrisk operations and conducting supply
chain traceability audits, and that they
are to share information with other
certifying agents to conduct audits and
verify compliance.
• AMS added the term supply chain
traceability audit to § 205.504(b)(7) to
more clearly state the need for and
objectives of the risk criteria and
procedures in this paragraph.
• AMS did not change
§ 205.501(a)(10), § 205.501(a)(13), or
§ 205.504(b)(4).
Summary of Public Comment
The majority of public comments
supported AMS’s proposed revisions to
recordkeeping requirements for certified
operations. Many comments noted that
including a description of full organic
status (e.g., ‘‘100 percent organic . . .’’)
on all records may be burdensome and
suggested that AMS allow the use of
abbreviations, acronyms, or shorthand
when identifying organic ingredients.
Other comments asked for additional
clarity about the definition of audit trail
and what types of documentation are
needed to meet the requirements of
§ 205.103(b)(3). Finally, a few comments
claimed that keeping full organic
identification on all records may be
burdensome and asked that AMS not
finalize this requirement in cases where
inventory management systems can
indicate organic status via lot codes or
batch numbers.
Comments largely supported AMS’s
proposed use of fraud prevention plans
by certified operations. However, many
comments requested additional
specificity about what should be
included in fraud prevention plans.
Other comments noted that fraud
prevention plans may be difficult for
very small businesses to write and
implement and recommended AMS
develop templates, examples, and
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generic forms for small operations to
use.
AMS received many comments about
the proposed definition of organic
fraud. Some comments requested that
AMS remove ‘‘illicit’’ and from the
definition, arguing that fraud may not
always constitute illegal activity. Others
suggested removing ‘‘intentional,’’ citing
the difficulty of proving intent. Several
comments also suggested AMS
harmonize the proposed definition with
existing definitions from other
organizations such as GFSI, the EU, ISO,
and FDA.
Public comment generally supported
the proposed use of supply chain
traceability audits. Many comments
asked AMS to clarify the requirements
of and extent of supply chain
traceability audits, particularly how far
back an audit should trace a product.
Others suggested adding a definition of
supply chain audit or traceability.
Opinions varied widely on the number
of supply chain traceability audits to be
conducted, with many comments
suggesting a minimum percentage of
operations or a risk-based selection.
Many comments also discussed the
administrative impacts of supply chain
traceability audits: a few comments
claimed some certifying agents may not
have the capacity of expertise to
conduct audits; others highlighted
challenges with information sharing and
coordination among certifying agents. A
few comments expressed a desire for
AMS to coordinate supply chain
traceability audits.
Finally, some comments suggested
alternatives to AMS’s proposed
traceability and fraud prevention
strategy, including trusted trader
programs, increased surveillance by
AMS, and exemptions for businesses
that already participate in other
traceability programs.
Responses to Public Comment
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Definition of Organic Fraud
(Comment) Comments asked AMS to
use ‘‘willful’’ instead of ‘‘intentional’’ in
the definition of organic fraud.
(Response) The rulemaking does not
use ‘‘willful’’ or ‘‘intentional’’ in the
final definition. This allows for a more
flexible definition that encompasses a
broader range of potential fraud types.
‘‘Willful’’ and ‘‘intentional’’ are not
needed because organic fraud is not
used for enforcement; it is used to help
explain the objective of this final rule
and many of its provisions.
(Comment) Comments asked AMS to
remove ‘‘for illicit economic gain,’’
claiming that not all fraud is illicit or
economic in nature. Comments also
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asked AMS to harmonize the definition
of organic fraud with terms used by
other standards organizations such as
ISO, GFSI, FDA, and the EU.
(Response) Many of the organizations
mentioned in public comment focus on
‘‘economic gain’’ as a key factor in
defining fraud. The final rule does not
include the phrase ‘‘for illicit economic
gain’’ because not all fraud results in or
is motivated by economic gain. This
definition is more flexible and
encompasses a broader range of
potential fraud types than terms used by
other standards organizations.
Recordkeeping
(Comment) Comments requested that
the regulatory text explicitly allow use
of abbreviations for indicating organic
status on records.
(Response) AMS amended
§ 205.103(b)(3) to allow use of similar
terms such as acronyms or abbreviations
for identifying organic status on audit
trail documentation. Abbreviations or
acronyms should be easily understood
to meet the requirement that all records
‘‘be readily understood and audited’’
(§ 205.103(b)(2).
(Comment) Comments are concerned
that the requirement to identify organic
products as such on all records will add
an unnecessary recordkeeping burden
that duplicates existing recordkeeping
or inventory management systems.
(Response) The requirement to
identify products as ‘‘100% organic,’’
‘‘organic,’’ or ‘‘made with organic
(specified ingredients or food
group(s)),’’ has been revised to apply
only to audit trail documentation. Other
records should also indicate organic
status to meet the requirement that all
records ‘‘be readily understood and
audited’’ (§ 205.103(b)(2)). However,
operations may use a system of
recordkeeping or inventory management
system that uses lot codes, batch
numbers, or other designation system
that indicates organic status, as long as
such designations are clear and
auditable.
(Comment) Commenters requested
clarity on the use of ‘‘internal’’ vs.
‘‘external’’ records for purposes of
supply chain traceability.
(Response) The requirements of
§ 205.103(b)(2) applies to broadly all
records maintained by an operation,
including both ‘‘external’’ and
‘‘internal’’ records. Section
205.103(b)(3) applies only to audit trail
documentation, i.e., ‘‘external’’ or
‘‘transaction’’ records.
Fraud Prevention Plans
(Comment) Comments asked AMS for
more detail about the scope of fraud
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3605
prevention plans and what elements
should be included in them.
(Response) The preamble of this
rulemaking describes best practices that
operations may use to develop and
implement fraud prevention plans. The
final regulatory text does not include
specific practices or requirements; this
provides maximum flexibility for
operations and certifying agents to
determine what is appropriate for
individual operations. A fraud
prevention plan must describe the
operation’s monitoring practices and
procedures they use to verify suppliers,
verify products received, and prevent
organic fraud. The plan must be
appropriately tailored to the activities,
scope, and complexity of the operation.
(Comment) Comments stated that the
fraud prevention plan requirement
would cause a disproportionate burden
(i.e., greater cost) on small operations,
especially small producers.
(Response) The final rule regulatory
text and the preamble explain that an
operation’s fraud prevention plan must
be appropriate to the operation’s
complexity, scope, and activities. This
may allow operations with less complex
activities and/or a more limited scope to
write and implement simpler fraud
prevention plans.
Supply Chain Traceability Audits
(Comment) Comments requested
greater clarity about the proposed rule’s
use of the terms traceback, massbalance, and supply chain audits.
(Response) Verification of traceability
back to the last certified operation and
mass-balance audits are routine practice
during on-site inspection of certified
operations. Section 205.403(d)(4)–(5)
describe the use of these mechanisms.
In contrast, supply chain traceability
audits are triggered by criteria defined
by the certifying agent. A supply chain
traceability audit generally encompasses
at least a portion of a supply chain and
is conducted to verify the compliance of
a product with the organic regulations
and the Act.
‘‘Traceback’’ is a term commonly used
in the organic industry. However, this
term was used inconsistently in public
comment and there was no clear
preference for how to define it.
Therefore, AMS has avoided using this
term in the final rule. AMS defines and
uses the term supply chain traceability
audit to describe certain activities, and
the regulatory text clarifies the extent of
other traceability requirements (e.g.,
§ 205.103(b)(2)) requires that an
operation’s records must be traceable
back to the last certified operation).
(Comment) Comments asked AMS for
clarification about the phrase ‘‘back to
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the source’’ in the proposed rule’s
revision to § 205.501(a)(21).
(Response) This phrase is not used in
the SOE final rule. The length and
extent of supply chain traceability
audits will vary depending on the
objective and findings of the process.
Some supply chain traceability audits
may extend back to the site of
production, while others may only go a
few steps back in a supply chain; the
audit ends when its objective (e.g.,
verification of compliance) is achieved.
(Comment) Many comments
discussed the administrative impacts of
supply chain traceability audits: a few
comments claimed some certifying
agents may not have the capacity or
expertise to conduct audits; others
highlighted challenges with information
sharing and coordination among
certifying agents.
(Response) Supply chain audits are an
important tool for oversight in the
organic market. AMS has added
flexibility for certifying agents to define
the conditions for when supply chain
audits are necessary. Further, there are
other requirements in this rule that will
Section
205.301 ...............................
205.400 ...............................
205.401 ...............................
The table below includes the
regulatory text related to this section of
the rule. A discussion of the policy
follows.
Product composition.
Paragraphs (f)(2) and (3).
General requirements for certification.
Paragraph (b).
Application for certification.
Paragraph (a).
R. Additional Amendments Considered
But Not Included in This Rule
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Q. Technical Corrections
Final regulatory text
AMS has revised § 205.301 to correct
a technical error in the description of
the prohibition of ionizing radiation and
sewage sludge. A previous technical
correction (80 FR 6429) contained an
error in the language used to describe
the prohibition on ionizing radiation
and sewage sludge. The terms
‘‘produced’’ and ‘‘processed’’ were
erroneously used to describe the use of
ionizing radiation and sewage sludge,
respectively, in the current regulatory
text. This action corrects the language at
paragraphs (f)(2) and (f)(3) to clarify that
all products labeled as ‘‘100% organic’’
or ‘‘organic’’ and all ingredients
identified as organic in the ingredient
statement of any product must not be
processed using ionizing radiation or
produced using sewage sludge.
AMS also revised §§ 205.400(b) and
205.401(a) to correct the references to
organic system plans (§ 205.201), which
was incorrectly cited in the previous
organic regulation.
The Strengthening Organic
Enforcement proposed rule asked the
public for feedback on two additional
subjects: packaged product labeling and
expiration of certification. AMS did not
propose amending the portions of the
USDA organic regulations that relate to
these subjects. The specific questions
asked in the proposed rule were meant
to elicit feedback from stakeholders
about the two topics for possible future
consideration. AMS has summarized the
public comment received below.
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support supply chain audits:
certification of additional handlers in
supply chains, mandatory NOP Import
Certificates, identifying organic
products on audit trail documentation,
and information sharing among
certifying agents.
18:59 Jan 18, 2023
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Summary of Public Comments:
Packaged Product Labeling
Processed and/or packaged food
products are often manufactured or
packaged by one business and labeled
for sale/distribution by another
business. This type of relationship,
sometimes called contract
manufacturing and private labeling, is
common in both the organic and
nonorganic markets. This rulemaking
does not change how such products are
labeled for retail sale. However, in the
proposed rule AMS asked for public
comment on private-labeled product
labeling, prompting feedback about
preferred terminology and which
businesses should be listed on labels.
Overall, there was no consensus
among comments about issues of
organic private-labeled products,
including who should be certified, what
terminology to use, and which
operations and certifying agents should
be listed on labels. Because private label
and brand/contract relationships are on
a contract-by-contract basis to protect
proprietary information, some
comments argued that creating a single
set of rules to govern these relationships
may change how private labels operate
in the future. The comments received
reflect this, and include a variety of
opinions based on a commenter’s
position in the organic supply chain.
Responses from public comments are
summarized below along with
background information to provide
context and help explain comments.
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Preferred Terminology To Describe
Private Label Products and Parties
Throughout the supply chain there
are many steps where brand companies
can leverage contracted companies to
produce items for sale under the brand.
After raw material sourcing, there are
opportunities for a company to contract
out steps such as manufacturing,
packaging, and distribution.
Because of the variable use and
function of contracted organizations in
organic production, it is important to
use common terminology to refer to
organic operations and their certifying
agents. Many comments requested
consistent regulatory terminology to
categorize these operations in relation to
the organic supply chain, but there was
no clear preference for certain
terminology. Terms and relationships
between contract food producers and
brand owners are highly variable in the
organic industry, but comments
highlighted opportunities to align with
commonly used and understood
terminology. Comments suggested terms
that could be consistently used to
prevent confusion about which
companies should appear on product
labels, including contract manufacturer
or ‘‘co-man,’’ contract packer or ‘‘copacker,’’ external distributors, Private
label entities/owners, and brand
owners.’’
Listing Contract Manufacturers on
Labels
The SOE proposed rule asked the
public if private label products or
brands that use contract manufacturers
should list those manufacturers on the
product label. The majority of
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comments supported optionally listing
contract manufacturers. Those who did
not agree with this opinion requested
that products should list the brand
name and the contract manufacturer.
Currently, it is mandatory for some
product categories such as meat,
poultry, and dairy to have an
Establishment Number that can trace
back to the facility where it was
processed. For other products that are
not currently mandated to provide this
information, identity of the contract
manufacturer is often considered
proprietary information, and in some
instances, there could be multiple
contract manufacturers operating at the
direction of one brand owner.
Commenters were concerned that
listing contract manufacturers would
result in a loss of competitiveness;
mandatory listings would expose
proprietary information and undercut
the success of these relationships. For
brand owners that use several
contracted companies, their products
would need multiple versions of labels
and traceability would become more
complex. Comments also questioned the
purpose of listing contract
manufacturers on labels, some arguing
that it would not improve organic
integrity or traceability, especially
because certifying agents are already
listed on products. Some comments
discussed that certifying agent
information is enough to trace the
product back to the manufacturer,
making the listing of contract
manufacturers unnecessary.
Listing Certified Operations on PrivateLabel Packaged Products
The organic regulations currently
require listing a certified operation on
branded products. The proposed rule
asked commenters which certified
operations should be added to the
packaging of private label products, in
the interest of furthering traceability.
Many comments recommend the brand
owner/distributor and their certifying
agent be listed on retail labels, with
some comments stating no preference.
Some commenters stated listing the
brand owner would require companies
to impose traceability standards on the
contract companies they use.
Some individuals recommend listing
the last certified operation in the supply
chain, to improve clarity and
traceability, while others contradict this
point by discussing the confidentiality
concerns of listing the contract
manufacturer. Commenters noted that
distributors may be the best certified
operation to list because they are often
the last step in the organic handling
process and can trace a product back
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through manufacturing and sourcing.
Conversely, others noted that not all
companies handle distribution
internally (choosing instead to use a
contracted company).
Other comments claim that listing copackers on labels is not necessary if
brand owners are certified; however,
some comments indicated it is unclear
if brand owners need to be certified.
Finally, a few comments recommended
AMS assess the labeling requirements’
alignment with the FDA.
Listing Certifying Agents on PrivateLabel Packaged Products
Multiple certifying agents are
typically involved in the production
and processing of organic products
(from raw materials to material refining,
manufacturing, and distribution); each
assures that an individual process or
step meets the organic standard. In the
case of brand companies with contract
manufacturers, comments did not
clearly agree on which certifying agent
(that of the brand company or that of the
contract manufacturer) to list on the
product label. Many individuals
supported listing the certifying agent of
the brand owner/distributor, but the
brand owner may not be certified. For
example, some comments pointed out
that retailers are often the brand
owners/distributors of organic products,
but they are often exempt from organic
certification. In this case, some
commenters recommended listing the
contract manufacturer’s certifying agent.
Others recommended listing the
certifying agent that certified that last
handling operation in the supply chain,
arguing that this would aid traceability.
However, due to the variety of different
manufacturing/branding relationships,
this could be either the certifying agent
of the brand owner or the manufacturer.
Matching the Certifying Agent to the
Listed Operation
Organic product labels currently must
include both a certifying agent and an
operation. Commenters generally agreed
that if a specific operation is listed (i.e.,
contract manufacturer), that the
certifying agent on the label should
match. Comments explained that
matching the two organizations would
make it easier to contact a responsible
party or file a complaint. Commenters
on the proposed rule also agree that a
label that lists the brand name next to
the contract manufacturer’s certifying
agent would be confusing. However,
given that some brand owners may not
be certified, commenters noted this
mismatch may already be happening in
the marketplace.
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Summary of Public Comments:
Expiration of Certification
Under current USDA regulation,
organic certification continues until
surrendered, revoked, or suspended
(§ 205.404(c)). Certified operations must
undergo an annual recertification
process (§ 205.406), but certification
does not expire after one year. While
developing the SOE proposed rule, AMS
considered, but did not propose, adding
a mechanism where certification would
expire if an operation did not complete
the annual recertification process
timely.
The proposed rule included specific
questions about expiration of
certification and asked the public to
comment on the subject. At this time,
AMS has chosen not to pursue a policy
of expiration of certification. The
following is a summary of public
comments received in response to the
questions AMS asked the public in the
SOE proposed rule.
Potential Improvements to Organic
Integrity
The SOE proposed rule asked the
public how annual expiration of
certification could improve organic
integrity. Some comments suggested
that expiration could be an incentive for
operations to punctually renew. Some
comments adverted that it may help
address the common incident of adverse
action circumstances by encouraging
operations to update their (organic
system plan) OSP and pay fees on time.
Commenters expressed if operations
understood the annual expiration date,
operations with unresolved
noncompliances would risk losing
certification via expiration. Those who
did not agree indicated that current
regulation specifies that operations are
certified unless suspended or revoked.
The annual expiration would disrupt
this current system of recertification.
Limitations of Expiration of
Certification
The proposed rule requested the
public to comment on what the
limitations of requiring expiration of
certification may be. Commenters
forecast potential negative effects such
as marketplace disruption,
communication burdens and
administrative burdens. Commentators
mentioned that expiration may
negatively impact the status of
inventory of operations who allowed
their certification to expire. One remark
stated that the requirement could place
additional administrative burden on the
certifying agent: expiration of
certification would result in the
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certifying agent having to update
systems, train staff, educate operations
on the policy change, and frequently
remind operations of the upcoming
expiration date.
Minimum Requirement for Renewing
Certification
The SOE proposed rule asked for
comments on what the minimum
requirement for renewing certification
should be. Many commenters
recommended the following process:
submit required paperwork, pay annual
fee, and confirm interest in renewing. It
was also recommended that on-site
inspection should not be a requirement
for recertification.
Operations With Adverse Actions
The proposed rule asked the public if
an operation with adverse actions that
are in the appeals process could renew
certification. Comments expressed
contrasting views on this matter, some
finding that operations should be able to
renew, and some communicating that
those operations should not have the
flexibility to renew their certification.
Some comments pointed out that the
appeal process for a proposed
suspension is lengthy, and that not
allowing an operation with pending
adverse actions to renew certification
would promptly remove them from the
system and prevent potentially
noncompliant product from entering the
market. Some individuals stated that
depending on the severity of the
pending adverse action, AMS should
administer a system that would not
block an operation from renewing its
certification due to minor noncompliances. Others asked that if an
operation has a record of failing to
address certain adverse actions, then the
system should prevent them from
renewing their certification.
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Grace Period for Renewing Certification
The SOE proposed rule asked
commenters if a grace period would be
appropriate for operations that failed to
renew by the expiration date.
Commenters were also asked what the
length of the grace period should be.
Overall, comments proffered a 30- or 90day grace period or mentioned that the
current system already has a grace
period built into the timeline. Some
individuals suggested that a grace
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18:59 Jan 18, 2023
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period would improve assurance among
farmers.
Process of Regaining Certification
The SOE proposed rule asked the
public to express their opinion on what
process should exist for an operation to
regain organic certification should they
allow it to expire. Many individuals
communicated that the process of
regaining an expired certification
should be different than regaining a
suspended/revoked certification. They
stated the process should also be
dependent on the presence and severity
of adverse actions and there should be
leniency within the duration. Some
commentators proposed that operations
with expired certification should apply
as a new applicant, unless applying
within the grace period. However, a
commenter identified a potential
loophole in tracking pending adverse
actions of operations with expired
certification; they recommended a
system that would keep a record of
operations with any pending adverse
actions.
Notification of Upcoming Expiration of
Certification
The SOE proposed rule asked the
public if certified agents should notify
certified operations of their upcoming
expiration of certification. Commenters
clarified that notifying certified
operations is currently a widespread
practice. Moreover, a commenter
suggested that notification should be
sent from the Organic Integrity
Database, which may normalize the
process.
IV. Regulatory Analyses
A. Summary of Economic Analyses
Executive Orders 12866 and 13563
control regulatory review.56 Executive
Orders 12866 and 13563 direct agencies
to assess all costs and benefits of
available regulatory alternatives, and, if
regulation is necessary, to select
regulatory approaches that maximize
net benefits (including potential
56 Executive Order 12866, Regulatory Planning
and Review, September 30, 1993: https://
www.archives.gov/files/federal-register/executiveorders/pdf/12866.pdf.
Executive Order 13563, Improving Regulation
and Regulatory Review: https://
www.federalregister.gov/documents/2011/01/21/
2011-1385/improving-regulation-and-regulatoryreview.
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economic, environmental, public health
and safety effects, distributive impacts,
and equity). Executive Order 13563
emphasizes the importance of
quantifying both costs and benefits,
reducing costs, harmonizing rules, and
promoting flexibility.
The Regulatory Flexibility Act (5
U.S.C. 601–612) requires agencies to
consider the economic impact of each
rule on small entities and evaluate
alternatives that would accomplish the
objectives of the rule without unduly
burdening small entities or erecting
barriers that would restrict their ability
to compete in the market.
This rulemaking amends amending
several portions of the USDA organic
regulations (7 CFR part 205) to
strengthen oversight and enforcement of
the production, handling, sale, and
marketing of organic agricultural
products in the United States. The
amendments address gaps in the organic
standards to deter organic fraud and
create a level playing field for farms and
businesses. This reinforces the value of
the organic label by assuring consumers
and stakeholders that organic products
meet a robust and consistent standard.
The revised organic standards in this
rule affect: certifying agents; certified
operations (farms, processers, and
handlers); and certain operations that
are currently excluded or exempt from
organic certification (e.g., certain
brokers, traders, importers, exporters).
The following discussion summarizes
the economic analysis AMS performed
to estimate the impacts of this rule. A
complete economic analysis of this
rulemaking is available at https://
www.regulations.gov/. You can access
the economic analysis by searching for
document number AMS–NOP–17–0065.
B. Regulatory Impact Analysis
The costs of this rule are primarily
due to new or additional reporting and
recordkeeping (paperwork) activities. In
addition, there is cost for some currently
excluded and exempt operations to
become certified to handle organic
products. AMS estimated the benefits of
this rule by quantifying the organic
fraud that will be prevented by
implementation of the rule. The
estimated benefits are expected to
outweigh the estimated costs. Total
estimated costs and benefits of the rule
are summarized below.
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COSTS AND BENEFITS OF RULEMAKING DISCOUNTED AT 3% AND 7%
Average annual cost a
Amendments
3% Discount
rate
I
7% Discount
rate
Total cost b
3% Discount
rate
I
7% Discount
rate
Domestic Certifying Agents
Imports to the United States ............................................................................
Certificates of Org. Operation & Cont. of Certification ....................................
Personnel Training & Qualifications ................................................................
On-Site Inspections .........................................................................................
Supply Chain Traceability & Organic Fraud Prevention ..................................
Mediation .........................................................................................................
$50,247
22,742
144,661
96,402
4,089
139
$37,534
21,892
108,061
72,012
3,054
134
$753,710
341,130
2,169,922
1,446,031
61,333
2,091
$563,016
328,377
1,620,918
1,080,176
45,815
2,013
6,236,939
276,243
125,240,844
5,547,100
93,554,079
4,143,647
673,763
454,968
13,529,496
9,135,993
10,106,444
6,824,526
7,884,601
6,550,892
14,435,494
24,272,099
158,227,651
131,545,210
289,772,861
494,172,179
118,269,011
98,263,398
216,532,409
364,081,491
Domestic Excluded Handlers
Applicability and Exemptions ...........................................................................
Imports to the United States ............................................................................
8,349,390
369,807
Domestic Certified Operations
Labeling of Nonretail Containers .....................................................................
Supply Chain Traceability & Organic Fraud Prevention ..................................
901,966
609,066
Total Costs and Benefits, Discounted Over 15 Years
Total
Total
Total
Total
a These
b These
Expected
Expected
Expected
Expected
Domestic Costs ...............................................................
Foreign c Costs ................................................................
Domestic & Foreign Costs ..............................................
Benefit of Rulemaking .....................................................
10,548,510
8,769,681
19,318,191
32,944,811
are the estimated annual averages of the 15-year Net Present Value domestic costs discounted at 3 and 7 percent.
are the estimated total domestic costs for affected industry in Net Present Value of the stream of future costs, discounted at 3 and 7
percent.
c AMS assumes all foreign costs will pass through to U.S. consumers and therefore includes these costs in the final rule. See the full Regulatory Impact Analysis for more detail.
khammond on DSKJM1Z7X2PROD with RULES2
Estimation of Benefits
AMS expects that this rule will
reduce organic fraud in the U.S. market.
Therefore, AMS quantified the
estimated benefits of the rulemaking as
the value of the projected reduction in
organic fraud in the U.S. organic
marketplace following implementation.
AMS reviewed economic studies that
identify and quantify fraudulent activity
in retail food markets. AMS then used
these estimates of fraud as a benchmark
to quantify the benefits of the
rulemaking.
Based on analysis of these food fraud
studies, AMS estimated that 2 percent of
organic products sold in the United
States are currently subject to some form
of fraud. This estimate aligns with rates
of food fraud reported in multiple
studies. Therefore, AMS estimated the
total value of organic fraud in the
United States as 2 percent of the total
annual organic premiums for domestic
organic production and organic imports,
or approximately $109 million annually.
AMS chose to use organic premiums
(the cost difference between organic and
nonorganic products) to estimate fraud
because this more accurately measures
the value lost to fraud than total sales
value (i.e., a fraudulent organic product
only loses the value of its organic
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attributes, not its entire value as a food
product).
AMS expects the changes from this
rule will reduce the amount of organic
fraud (estimated at $109 million
annually) by half (an estimated $54
million). However, it is unclear what
proportion of this $54-million fraud
reduction translates directly into social
welfare loss. For example, some
certified operations and other compliant
entities in organic supply chains may
unknowingly experience some
economic gain from fraud elsewhere in
the supply chain. Additionally, AMS
cannot accurately predict how fraud
reduction efforts would impact organic
prices, and hence premiums. Given this
uncertainty about the true value of
social welfare loss, AMS reduced the
estimated $54 million fraud reduction
by half for an estimated social welfare
gain (benefit) of $27 million in the first
year following implementation of the
rule. Estimated over a 15-year period,
and accounting for projected future
annual growth rates of the U.S. organic
market, annual benefits from fraud
reduction are estimated to reach $57
million in year 2036. When discounted
over the 15-year period, total economic
benefits of the rulemaking range from
$364 to $494 million. When averaged,
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the economic benefits range from $24.3
to $32.9 million annually.
Estimation of Costs
The costs of this rule are driven
primarily by new or additional reporting
and recordkeeping (paperwork)
activities. AMS estimated additional
paperwork cost for each provision of the
rule by identifying the affected
population (e.g., number of producers
affected by a change), estimating the
time for each affected entity to comply
with a new change, and assigning an
appropriate labor category and wage
rate. This accounting of new reporting
and recordkeeping costs is discussed in
more detail in the Paperwork Reduction
Act section of this rulemaking.
This rule would also require some
currently excluded and exempt
operations to become certified to handle
organic products. AMS predicts that
these businesses fall within NAICS
categories 425 (Wholesale Electronic
Markets and Agents and Brokers) and
4244 (Grocery and Related Product
Merchant Wholesalers). These categories
are very broad and include mostly
businesses that do not handle organic
products. Therefore, AMS used
participation rates in the organic sector
to estimate that 1,985 domestic
businesses would need to become
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certified organic. Using historic
knowledge of certification costs, AMS
estimated that each of the affected 1,985
domestic businesses would spend
$2,000 to become certified organic.
AMS also estimated the cost of this
rule to foreign entities, including both
paperwork and recordkeeping burden
and costs for certain businesses to
obtain certification. AMS assumes that
all foreign costs will be passed along to
U.S. consumers. This may create some
tendency to overstate U.S.-borne costs,
as competitive pressures will lead some
compliance costs to be absorbed by
businesses and other entities as the cost
of doing business.
Alternatives
AMS also considered three
alternatives when developing this
rulemaking.
1. Make no change to the organic
regulations. This option would not
implement this rulemaking and leave
the organic regulation as-is. AMS did
not select this option because it does not
address organic fraud or other issues
affecting organic integrity. AMS
considers this a costly alternative
because it forgoes the fraud reduction
benefits of the rulemaking. Regulatory
inaction would create social costs that
increase over time. AMS believes the
rulemaking will mitigate social welfare
losses by approximately half through
the use of practical, risk-based oversight
and enforcement.
2. Require NOP Import Certificates for
individual imported shipments of
organic product. The rulemaking will
allow NOP Import Certificates to be
issued for multiple shipments over a
time span to be determined at the
discretion of each certifying agent. In
contrast, this alternative would require
the use of NOP Import Certificates for
each physical shipment of organic
products imported into the United
States. AMS found this alternative to be
inferior to the rulemaking because it
would create greater cost with limited
additional benefit. AMS believes that
the rulemaking’s option to issue NOP
Import Certificates on a periodic basis is
the most practical, effective, and costsensitive means to address fraudulent
imported organic products.
3. Require less-stringent data
reporting and training requirements for
certifying agents. AMS also considered
a less-stringent alternative to the
rulemaking to assesses if this could
lower costs while maintaining the
effectiveness of the rulemaking. Relative
to the rulemaking, this alternative
would (1) omit the requirement for
certifying agents to issue standardized
certificates of organic operation
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generated in the USDA Organic Integrity
Database; and (2) reduce the annual
training hours that must be completed
by organic inspectors and certification
review personnel. AMS chose not to
pursue this alternative because it would
weaken other critical, interdependent
amendments in the rulemaking. AMS
predicts any cost reduction of this
alternative would be accompanied by a
significant reduction in effectiveness of
the rulemaking.
Regulatory Flexibility Act
AMS also performed additional
analysis to determine the rule’s impact
to domestic small businesses. This
analysis revealed that small businesses
producing, selling, handling, and
marketing organic products would not
be adversely affected by the
amendments in this rule. AMS expects
that most of the entities affected by this
rule are small businesses as defined by
Small Business Administration criteria.
For each category of affected entity
(certifying agents, certified operations,
and exempt or excluded operations that
need to become certified), AMS
estimates that the costs of the rule for
each business type will be less than one
percent of the annual revenue.
A full economic analysis of this
rulemaking is available at https://
www.regulations.gov/. You can access
this rule and the economic analysis by
searching for document number AMS–
NOP–17–0065.
C. Executive Order 12988
Executive Order 12988 instructs each
executive agency to adhere to certain
requirements in the development of new
and revised regulations in order to avoid
unduly burdening the court system.
This rule cannot be applied
retroactively. States and local
jurisdictions are preempted under the
OFPA from creating programs of
accreditation for private persons or state
officials who want to become certifying
agents of organic farms or handling
operations. A governing state official
would have to apply to USDA to be
accredited as a certifying agent, as
described in section 6514(b) of the
OFPA. States are also preempted under
sections 6503 through 6507 of the OFPA
from creating certification programs to
certify organic farms or handling
operations unless the state programs
have been submitted to, and approved
by, the Secretary as meeting the
requirements of the OFPA.
Pursuant to section 6507(b)(2) of the
OFPA, a state organic certification
program that has been approved by the
Secretary may contain additional
requirements for the production and
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handling of agricultural products
organically produced in the state and for
the certification of organic farm and
handling operations located within the
state under certain circumstances. Such
additional requirements must (a) further
the purposes of the OFPA, (b) not be
inconsistent with the OFPA, (c) not be
discriminatory toward agricultural
commodities organically produced in
other States, and (d) not be effective
until approved by the Secretary.
In addition, pursuant to section
6519(c)(6) of the OFPA, this rulemaking
does not supersede or alter the authority
of the Secretary under the Federal Meat
Inspection Act (21 U.S.C. 601–624), the
Poultry Products Inspection Act (21
U.S.C. 451–471), or the Egg Products
Inspection Act (21 U.S.C. 1031–1056),
concerning meat, poultry, and egg
products, respectively, nor any of the
authorities of the Secretary of Health
and Human Services under the Federal
Food, Drug and Cosmetic Act (21 U.S.C.
301–399), nor the authority of the
Administrator of the Environmental
Protection Agency under the Federal
Insecticide, Fungicide and Rodenticide
Act (7 U.S.C. 136–136(y)).
OFPA at 7 U.S.C. 6520 provides for
the Secretary to establish an expedited
administrative appeals procedure under
which persons may appeal an action of
the Secretary, the applicable governing
State official, or a certifying agent under
this title that adversely affects such
person or is inconsistent with the
organic certification program
established under this title. The OFPA
also provides that the U.S. District Court
for the district in which a person is
located has jurisdiction to review the
Secretary’s decision.
D. Paperwork Reduction Act
In accordance with the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520) (PRA), AMS is requesting OMB
approval for a new information
collection totaling 368,321 hours for the
reporting and recordkeeping
requirements contained in this
rulemaking. OMB previously approved
information collection requirements
associated with NOP and assigned OMB
control number 0581–0191. AMS
intends to merge this new information
collection (0581–0321), upon OMB
approval, into the approved 0581–0191
collection. Below, AMS has described
and estimated the annual burden (i.e.,
the amount of time and cost of labor),
for entities to prepare and maintain
information to participate in this
voluntary labeling program. The
Organic Foods Production Act of 1990
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(OFPA) provides authority for this
action.57
Title: National Organic Program.
OMB Control Number: 0581–0321.
Expiration Date of Approval: 3 years
from OMB date of approval.
Type of Request: New collection.
Abstract: Information collection and
recordkeeping are necessary to
implement reporting and recordkeeping
necessitated by amendments to §§ 205.2,
205.100, 205.101, 205.103, 205.201,
205.273, 205.300–205.302, 205.310,
205.307, 205.310, 205.400, 205.403–
205.404, 205.406, 205.500–501, 205.504,
205.511, 205.660–205.663, 205.665,
205.680, and 205.681 of the USDA
organic regulations. The rulemaking
will protect organic product integrity
and build consumer and industry trust
in the USDA organic label by
strengthening organic control systems,
improving organic import oversight,
clarifying organic certification
standards, and enhancing farm to
market traceability.
This rulemaking amends several
sections of the USDA organic
regulations, 7 CFR part 205, to
strengthen the NOP’s ability to oversee
and enforce the production, handling,
marketing, and sale of organic
agricultural products as established by
the OFPA. The rule will improve
organic integrity throughout the organic
supply chain and benefit stakeholders at
all levels of the organic industry. The
amendments will close gaps in the
current regulations to build consistent
certification practices, deter organic
fraud, and improve transparency and
product traceability. NOP identified the
need for many of the amendments as
part of its direct experience in
administering this program, particularly
via complaint investigation and audits
of certifying agents. Other amendments
are based on changes to the OFPA
included in the Agriculture
Improvement Act of 2018; 58 the
recommendations of a 2017 Office of
Inspector General audit; 59 the
57 The Organic Foods Production Act of 1990, 7
U.S.C. 6501–6524, is the statute from which the
Agricultural Marketing Service derives authority to
administer the NOP, and authority to amend the
regulations as described in this rulemaking. This
document is available at: https://uscode.house.gov/
view.xhtml?path=/prelim@title7/
chapter94&edition=prelim.
58 The Agriculture Improvement Act of 2018
(Public Law No: 115–334), commonly known as the
‘‘2018 Farm Bill,’’ is available at https://
www.congress.gov/115/plaws/publ334/PLAW115publ334.pdf. Organic certification is discussed
in Title X, Section 10104.
59 The National Organic Program International
Trade Arrangements and Agreements Audit Report
01601–0001–21, September 2017: https://
www.usda.gov/sites/default/files/01601-000121.pdf.
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recommendations of the National
Organic Standards Board (a federal
advisory committee to NOP); and
industry stakeholder feedback.
This rulemaking strengthens
enforcement with amendments to the
USDA organic regulations and modifies
the reporting and recordkeeping
burdens as summarized below.
1. Reduces the types of uncertified
handling operations in the organic
supply chain that operate without
USDA oversight.60 The amendments
require certification of operations that
facilitate the sale or trade of organic
products, including but not limited to
certain brokers, importers, and traders.
These handlers must obtain organic
certification and develop an organic
system plan (OSP) to describe the
practices and procedures used in their
operations. Certifying agents customize
the format of the OSP to cover standards
applicable to operations seeking
certification. Because traders and
brokers do not farm or manufacture
organic products, the OSPs for traders
and brokers will address fewer sections
of the organic regulations than OSPs for
operations that farm or manufacture
organic products. Therefore, uncertified
traders and brokers will take 40 hours
in the first year after the rule going into
effect to prepare an initial OSP. In
subsequent years, AMS estimates each
of these entities will incur a
recordkeeping burden of 10 hours
annually, and a reporting burden of 20
hours annually, to update their OSP
(§§ 205.2, 205.100, 205.101, and
205.103).
Burden is increased in the rulemaking
due to refinements in NAICS code 425
and the addition of operations from
NAICS code 4244 in response to public
comment. The 2018 Farm Bill mandates
that NOP reduce the number of
operations excluded from certification
at § 205.101. AMS’s revised estimate
indicates 1,985 formerly excluded
domestic operations now require
organic certification. This includes 855
operations in NAICS code 425
(Wholesale Electronic Markets and
Agents and Brokers) and 1,130
operations in NAICS code 4244 (Grocery
and Related Product Merchant
Wholesalers). See the accompanying
Regulatory Impact Analysis (RIA) for
more information. AMS assumes the
1,985 domestic excluded operations
represent 59 percent of the global total
of excluded handlers (using a
benchmark 59 percent to 41 percent
ratio of domestic to foreign operations).
Therefore, AMS estimates there are an
60 Mandated by the Agriculture Improvement Act
of 2018. See section 10104(a).
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3611
additional 1,379 foreign formerly
excluded operations, for a total of 3,364
new handlers that will need organic
certification.
2. Requires all currently certified
organic operations and new applicants
to describe their procedures for
monitoring, verifying, and
demonstrating the organic status of their
suppliers and products received to
prevent organic fraud. Operations will
include this information as a
supplemental part of the OSP; therefore,
AMS allocates the time to develop these
procedures separately from the initial 40
hours to develop an OSP. AMS
estimates that each currently certified
operation and applicant seeking
certification will need 30 minutes to
describe the supply chain verification
procedures and monitoring practices
required by this regulation (§§ 205.103
and 205.201). Burden is increased in the
rulemaking due to industry growth.
3. Mandates the use of NOP Import
Certificates. Each shipment of organic
products imported into the United
States must be declared as organic to
U.S. Customs and Border Protection
(CBP) and associated with a valid NOP
Import Certificate (currently form NOP
2110–1).61 The NOP Import Certificate
contains specific information about the
quantity and source of a shipment of
imported organic products. NOP Import
Certificates are currently used for
organic products imported from
countries with which NOP has trade
arrangements. This rulemaking will
expand and make compulsory the use of
NOP Import Certificates, regardless of
an imported product’s country of origin.
In response to public comments, the
final rule allows NOP Import
Certificates to be issued for a given time
period (e.g., quarterly) rather than with
every shipment as proposed. AMS
estimates that NOP Import Certificates
will be issued quarterly, as this will
reduce costs and limit disruption to the
speed of imports. Additionally, the
estimated number of annual shipments
has increased from 67,023 in 2017 to
80,109 in 2020 due to industry
growth.62 Therefore, AMS estimates
3,856 exporters will request from their
certifying agents an annual total of
15,424 NOP Import Certificates,
61 Office of Management and Budget (OMB)
approved form NOP 2110–1 NOP Import Certificate.
https://www.ams.usda.gov/resources/nop-2110-1.
62 Data source: USDA Foreign Agricultural
Service (FAS) Global Agricultural Trade System
(GATS). Select: Partners, World Total, Product
Type, Imports—General, Products: All Aggregates;
Product Groups: Organic—Selected: https://
apps.fas.usda.gov/gats/default.aspx.
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covering 80,109 annual shipments.63
AMS estimates each exporter and
certifying agent will spend an average of
30 minutes to request and approve each
NOP Import Certificate. This estimate
accounts for some learning within the
first year, as well as the option to issue
a single NOP Import Certificate for
multiple shipments over a specific
timeframe and amount or volume.
Additionally, AMS estimates that
importers and their certifying agents
will need an average of one tenth (0.1)
of an hour, or 6 minutes, to compare the
shipping manifest of each shipment
with its respective NOP Import
Certificate to verify the accuracy and
organic compliance of each shipment.
Further, certifying agents must have
and implement a documented organic
control system for intaking and
approving or rejecting the validity of an
NOP Import Certificate request, and
importers must have and implement a
documented organic control system to
verify that shipments of organic
products are accompanied by accurate
NOP Import Certificate data and have
not had contact with prohibited
substances or ionizing radiation
(§§ 205.273 and 205.300).
4. Clarifies nonretail containers used
to ship or store organic products must
display organic identification and
information that links the container to
audit trail documentation. This will
help maintain the integrity of organic
products by reducing misidentification
and mishandling, facilitating
traceability through the supply chain,
reducing organic fraud, and allowing
accurate identification of organic
product by customs officials and
transportation agents.
The rulemaking reduces burden
because the revised regulation requires
less information on nonretail container
labels and provides exceptions for
certain types of containers in response
to public comment. AMS estimates that
35,698 producers and/or processers will
need one tenth (0.1) of an hour, or 6
minutes, to add the required
information to the labels that are
displayed on the nonretail containers of
an estimated 275,596 annual shipments
(§ 205.307).64
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63 NOP
International Division reports that 3,303
organic exporters are certified by foreign (nonUSDA) certifiers. Plus, the Organic Integrity
Database shows that 553 foreign-based handlers are
certified by USDA-accredited certifying agents. The
total number of NOP Import Certificates assumes
each exporter is issued NOP Import Certificates
quarterly (four annually).
64 29,929 (existing and new domestic operations
and traders) certified operations will be modifying
how they label 195,387 nonretail shipments and
5,769 (existing, new, and domestic operations and
traders) certified operations will be modifying how
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5. Codifies current practices for the
certification of producer group
operations (groups of producers
organized and certified as a single
operation).65 The rulemaking describes
the criteria to qualify as a producer
group, how producer group operations
must comply with the USDA organic
regulations, and how certifying agents
should inspect these operations. It also
sets a risk-based benchmark to
determine how many producer group
members in an operation need to be
inspected by certifying agents annually.
In response to public comment, AMS
expects that these requirements will add
11,800 hours of one-time paperwork
burden for 5,900 producer group
operations 66 to prepare a detailed
Internal Control System for their OSP,
including procedures to address
conflicts of interest and manage the
unique challenges of producer group
oversight. In addition, AMS estimates 5
hours to prepare and deliver training,
outreach and technical assistance to ICS
personnel and producer group members,
leading to a total annual burden of
29,500 hours of burden annually
(§§ 205.201, 205.400(g) and 205.403).
6. Clarifies how certified operations
may submit annual updates to their
OSP. This includes the option to only
submit practices or procedures that have
changed since their last approved OSP,
rather than submitting an OSP in its
entirety. This will reduce unnecessary
paperwork without compromising
oversight because operations will
continue to maintain an OSP that
accurately reflects current practices and
procedures of the operation. This
codifies current policy and does not
modify the paperwork burden
(§ 205.406).
7. Requires certifying agents to issue
standardized certificates of organic
operation generated from the USDA’s
publicly available Organic Integrity
Database (OID).67 This will require an
initial upload of mandatory data for
each operation and maintenance to
ensure that data in OID are current and
accurate. Currently, all certifying agents
have voluntarily uploaded data and
maintain an estimated 50% or more data
they label 80,109 nonretail shipments exported to
the US.
65 NOP Policy Memo 11–10. Grower Group
Certification, October 31, 2011: https://
www.ams.usda.gov/sites/default/files/media/NOP11-10-GroupGrowerCert.pdf.
66 Meinshausen F., Richter, T., Blockeel, J., and
Huber, B., Group Certification: Internal Control
Systems in Organic Agriculture: Significance,
Opportunities and Challenges, Research Institute of
Organic Agriculture FiBL, March 2019.
67 Organic Integrity Database: https://
organic.ams.usda.gov/integrity. Accessed
September 2021.
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on all certified operations per the
recommendations found in the NOP’s
Data Quality Best Practices.68
These amendments will require a
new, one-time burden of reporting hours
for certifying agents to upload existing
data pertaining to currently certified
operations into OID for the first time. It
is estimated that uploading these data
into OID will require 30 minutes for
each operation and will be performed by
administrative support personnel who
have a lower wage rate than review and
compliance staff. The rulemaking’s
burden increases slightly due to
industry growth.
These amendments will
simultaneously eliminate the
requirement to physically mail the
Administrator or State organic program
paper copies of: (1) the list of operations
certified annually; (2) notifications of
proposed adverse actions, approvals, or
denials of corrective actions; and (3)
notifications of executions of adverse
actions regarding certified operations or
operations applying for certification
(§§ 205.405 and 205.501). AMS is not
modifying the estimate of paperwork
burden associated with these changes in
requirements because any change will
be very small, and these activities and
tasks are still occurring electronically as
a part of maintaining the data on all
operations over time.
8. Requires certifying agents to
develop procedures to: (1) identify highrisk operations and agricultural
products; (2) conduct supply chain
traceability audits, (3) share information
with other certifying agents to verify
supply chains and conduct
investigations, and (4) report credible
evidence of organic fraud to the USDA.
Due to the complexity of these
procedures, AMS estimates each
certifying agent will spend two hours
documenting these procedures
(§§ 205.501 and 205.504) rather than
one hour as proposed. The rulemaking’s
burden increases due to an increase in
time for preparing procedures despite a
net loss of certifying agents since 2017
(the net value reflects that while some
certifiers have been suspended or have
surrendered, others have been newly
accredited).
9. Requires certifying agents to submit
their decision criteria for acceptance of
mediation, and a process for identifying
personnel to conduct mediation and set
up mediation sessions with its
administrative policies and procedures
required by § 205.504(b). AMS estimates
each certifying agent will spend one
68 Data Quality Best Practices: https://
www.ams.usda.gov/sites/default/files/media/
INTEGRITY%20Data%20Quality.pdf.
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hour documenting these procedures,
which they are already implementing.
The rulemaking’s burden changes due to
the net loss of 3 certifying agents since
2017.
10. Requires certifying agents to
establish procedures to conduct
inspector field evaluations (‘‘witness
inspections’’), demonstrate that they are
sufficiently staffed with qualified
personnel, and demonstrate that all
inspectors, certification reviewers, and
in-field evaluators meet knowledge,
skills, and experience qualifications.
AMS estimates that each certifying
agent will spend 60 minutes to draft
policies and procedures for conducting
inspector field evaluations. Further,
certifying agents must observe an
inspector performing an on-site
inspection at least once every three
years (or annually for inspectors with
fewer than three years of experience).
The rulemaking’s burden is reduced
due to narrowed training requirements
and the net loss of 3 certifying agents
since 2017. AMS estimates each
certifying agent will conduct an average
of two field evaluations of an inspector
and certification review personnel per
year, rather than four as proposed, and
that this activity will require 7.5 hours
per evaluation (§§ 205.2 and 205.501).
11. Requires some additional training
of new inspectors and certification
review personnel. Inspectors and
certification review personnel play a
crucial role in determining whether an
operation is granted organic certification
initially and whether certified
operations comply with the USDA
organic regulations. Certification review
personnel may also serve as inspectors.
Through insight gained during regular
audits of certifying agents, AMS
estimates that inspectors and
certification review staff currently
receive at least 10 hours of training per
year from certifying agents on topics
related to the USDA organic regulations.
In response to public comment, 40
hours of additional training is required
for inspectors and certification review
personnel with less than one year of
experience.69 Based on an estimated
separation rate of 14 percent, 70 AMS
69 Ten hours of training are accounted for in the
2020 Information Collections Renewal for NOP
(AMS–NOP–19–0090; OMB Control Number: 0581–
0191). Our internal on-site accreditation audit
checklist used by our accreditation audit team
includes a question on training. With the
implementation of this rule, the specific hours of
training offered by the 75 certifying agents will be
documented.
70 The US Bureau of Labor and Statistics reports
that the average separation rate (which captures
both labor force exits and transfers in occupation)
for agricultural inspectors is 14 percent. https://
www.bls.gov/news.release/jolts.t16.htm.
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estimates that certifying agents will
annually hire 35 new certification
review staff and hire or contract with 35
inspectors with less than one year of
experience to replace the certification
review staff and inspectors that exit the
labor pool. Training offered by NOP
through its online Organic Integrity
Learning Center (OILC) and training
provided by the certifying agents or
other providers may qualify towards the
minimum annual training requirements
(§§ 205.2 and 205.501).
12. Requires that certifying agents
conduct unannounced inspections of at
least 5 percent of the operations they
certify, which is the current
recommended practice in NOP
Instruction 2609.71 For the purposes of
estimating paperwork impacts, AMS
expects that half of the unannounced
inspections (2.5% of total inspections)
will meet the requirement for a full
annual inspection and will not impact
current paperwork burden. The
remaining half of the unannounced
inspections (2.5% of total inspections)
will be limited in scope and target highrisk operations and will not count as a
full annual inspection. Examples of
targeted, limited-scope unannounced
inspections include but are not limited
to verifying livestock on pasture or
performing targeted mass-balance or
traceability audits. AMS estimates that
the paperwork impacts associated with
these unannounced inspections will
average inspectors 5 hours per
inspection; half of the estimated 10
hours for a full annual inspection
(§ 205.403).
13. Clarifies the process for accepting
foreign conformity assessment systems
that oversee organic certification in
foreign countries.72 The OFPA (7 U.S.C.
6505(b)) and the USDA organic
regulations provide the authority to
establish organic equivalency. The
revised regulations describe the criteria,
scope, and other parameters for ongoing
peer review audits of foreign organic
conformity systems to determine
whether the United States should
continue, revise, or terminate such
equivalence determinations. These peer
review audits of equivalence
determinations occur as needed and
will result in new periodic paperwork
impacts for foreign governments. The
71 NOP 2609, Instruction, Unannounced
Inspections. September 12, 2012. Available in the
NOP Program Handbook: https://
www.ams.usda.gov/sites/default/files/media/
2609.pdf.
72 Currently, the United States has established
organic trade arrangements with Canada, the
European Union, the United Kingdom, Israel, Japan,
New Zealand, South Korea, Taiwan, and
Switzerland.
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3613
rulemaking’s burden is reduced because
AMS estimates it will review one
foreign government conformity
assessment system per year. AMS
estimates the reporting impacts for
foreign governments when USDA
reviews the applicable trade
arrangement or agreement to be 60
hours. Since recordkeeping is ongoing
requirement, recordkeeping is
calculated as 10 hours per year per
foreign government. These impacts are
comparable to the estimated paperwork
impacts for AMS audits of certifying
agents (§ 205.511).
Respondents
AMS has identified four primary
types of entities (respondents) that will
need to submit and maintain
information as a result of this
rulemaking: certified organic operations;
accredited certifying agents; organic
inspectors; and foreign governments.
Three respondent types—certified
operations (producers and handlers),
certifying agents, and inspectors—have
been identified in a currently approved
information collection (0581–0191). To
implement a 2018 Farm Bill mandate,
AMS is requiring certification of
additional types of operations in the
organic supply chain and regular audits
of trade arrangements or agreements
with foreign governments.73 This adds
new types of handlers as a subcategory
of certified operations and foreign
governments as a new type of
respondent.
To more precisely understand the
paperwork impacts of this rulemaking,
AMS has divided the categories of
respondents into domestic and foreign,
as appropriate, to show the potential
impacts on domestic-based versus
foreign-based USDA-accredited
certifying agents, inspectors, and
certified operations, along with foreignaccredited certifying agents, and foreign
governments serving as accrediting
bodies. For each type of respondent, we
describe the general paperwork
submission and recordkeeping activities
and estimate: (1) the number of
respondents; (2) the hours they spend,
annually, creating and storing records to
meet the paperwork requirements of the
organic labeling program; and (3) the
costs of those activities based on
prevailing domestic and foreign wages
and benefits.
Certifying Agents
Certifying agents are State, private, or
foreign entities accredited by the USDA,
73 See Section 10104(a) of the Agriculture
Improvement Act of 2018, Public Law No: 115–334,
available at: https://www.congress.gov/115/plaws/
publ334/PLAW-115publ334.pdf.
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or by accreditation bodies of foreign
governments with which USDA has a
trade arrangement or agreement.
Certifying agents certify domestic and
foreign producers and handlers as
organic in accordance with the OFPA
and the USDA organic regulations.
Certifying agents determine whether a
producer or handler meets the organic
requirements, using detailed
information from the operation about its
specific practices and on-site inspection
reports from organic inspectors.
Currently, there are 75 USDAaccredited certifying agents (down from
78 in 2017) 45 are based in the United
States and 30 are headquartered in
foreign countries. Both domestic- and
foreign-based USDA-accredited
certifying agents certify operations
based in the United States and abroad.
AMS assumes all currently accredited
certifying agents evaluate all types of
production and handling operations for
compliance with the USDA organic
regulations and will be subject to the
reporting and recordkeeping burdens of
this rulemaking. In addition, AMS
assumes there are 30 foreign
government-accredited foreign-based
certifying agents that certify handlers in
accordance with the USDA organic
regulations and that will issue NOP
Import Certificates for organic product
shipments to the United States.74
Certifying agents of operations that
export to the United States must issue
NOP Import Certificates for all
shipments of organic products being
exported. The USDA Foreign
Agricultural Service (FAS) Global
Agricultural Trade System (GATS)
showed 80,109 shipments of organic
product coming into the United States
in 2020 (up from 67,023 in 2017 due to
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74 An estimate based on the number of foreignbased USDA-accredited certifying agents.
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industry growth).75 In response to
public comments, AMS estimates that
NOP Import certificates will be issued
seasonally (e.g., quarterly) rather than
with every shipment as proposed. AMS
estimates that 3,856 foreign exporters
will request from their certifying agents
an annual total of 15,424 NOP Import
Certificates, covering 80,109 annual
shipments.76 AMS estimates each
exporter and certifying agent will spend
30 minutes to request and approve each
NOP Import Certificate.
Thirty (30) USDA-accredited
certifying agents based in foreign
countries certify 92% of the foreign
operations certified under USDA
organic standards. Of the 45 domesticbased USDA accredited certifying
agents, 15 certifying agents certify 8% of
the foreign operations certified under
USDA.77 This means that 30 domesticbased USDA-accredited certify agents
only certify domestic-based operations
that do not import foreign organic
products or ingredients. AMS estimates
there are 30 foreign-accredited certifying
agents that certify foreign operations
under trade arrangements.78
AMS will review documents
regarding imports during the
75 Data source: USDA Foreign Agricultural
Service (FAS) Global Agricultural Trade System
(GATS). Select: Partners, World Total, Product
Type, Imports—General, Products: All Aggregates;
Product Groups: Organic—Selected: https://
apps.fas.usda.gov/gats/default.aspx.
76 NOP International Division reports that 3,303
organic exporters are certified by foreign (nonUSDA) certifiers. Plus, the Organic Integrity
Database shows that 553 foreign-based handlers are
certified by USDA-accredited certifying agents. The
total number of NOP Import Certificates assumes
each exporter is issued NOP Import Certificates
quarterly (four annually).
77 Organic Integrity Database: https://
organic.ams.usda.gov/integrity/.
78 An estimate based on the number of foreignbased USDA-accredited certifying agents.
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accreditation audits of USDA-accredited
certifying agents. AMS estimates 30
minutes for the 3,856 exporters and
their certifying agents to prepare and
approve each of the 15,424 NOP Import
Certificates and one tenth of an hour, or
6 minutes, for importers to verify and
reconcile all 80,109 subsequent
associated shipments exported to the
United States.76 USDA-accredited
domestic-based certifying agents must
work with their foreign-based
operations to verify their associated
shipments for 8%, or 6,409, of 80,109
annual shipments. USDA-accredited
foreign-based certifying agents must
work with their foreign-based
operations to verify their associated
shipments for 46%, or 36,850, of 80,109
annual shipments. Foreign-accredited
certifying agents must work with their
foreign-based operations to verify 46%
of 80,109 annual shipments.
In addition, this rulemaking reduces
the current paperwork burden of
accredited certifying agents by
eliminating the need to provide notices
of approval or denial of certification to
the Administrator following the
issuance of a notice of noncompliance
or adverse action to an applicant for
certification. Also, the rulemaking
removes the annual requirement for
certifying agents to submit by January 2
an annual list of operations certified.
Certifying agents will instead be
required to update data in OID for each
operation they certify. AMS is not
modifying the estimate of paperwork
burden with these changes in
requirements because any change will
be very small. These activities and tasks
are still occurring electronically as a
part of maintaining the data on all
operations over time. Certifying agents
must issue organic certificates generated
in OID.
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In addition, all USDA-accredited
certifying agents must write detailed
procedures to identify high-risk
operations and products they certify and
procedures to conduct supply-chain
traceability audits. Certifying agents
must write fraud prevention and
reporting procedures, and mediation
procedures per § 205.504(b). Certifying
agents must write procedures to
demonstrate how they are sufficiently
staffed and that all persons who perform
certification review activities and onsite inspections (inspectors) are
qualified and complying with training
requirements for their new certification
review personnel. AMS estimates that
14 percent, or 35, new certification
review staff with less than one year of
experience must complete 40 hours of
training in their first year in addition to
the baseline training requirement of 10
hours annually already accounted for in
the overall program ICR (0191).79 80
This rulemaking increases the overall
reporting and recordkeeping burden for
certifying agents (See Summary Table 1:
Certifying Agents). AMS estimates the
annual collection cost per domesticbased USDA-accredited certifying
agents will be $13,511.81 This cost is
based on an estimated 109.23 labor
hours per certifying agent per year for
staff with certification review
responsibilities at $47.97 per labor hour,
including 31.7% benefits, for a total
salary component of $5,229 per year.82
The estimated cost for domestic
certifying agents also includes 332.55
labor hours per certifying agent per year
for administrative support staff to
upload data about certified operations to
OID at $24.90 per labor hour, including
3615
31.7% benefits, for a total salary
component of $8,282 per year.83
In addition, AMS estimates the
annual collection cost for all domesticbased USDA-accredited certifying
agents will be $608,001. This cost is
based on a total of 4,915 hours for all
staff with certification review
responsibilities at $47.87 per labor hour,
including 31.7% benefits, for a total
salary component of $235,313 for all
staff with certification review and
procedure writing responsibilities of all
domestic-based USDA-accredited
certifying agents. The estimated cost for
all domestic-based certifying agents also
includes 14,965 hours total hours for
administrative support staff uploading
data about certified operations to OID at
$24.90 per labor hour, including 31.7%
benefits for a total salary component of
$372,688.
SUMMARY TABLE 1—CERTIFYING AGENTS
Number of
respondents
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Respondent categories
Wages +
benefits
Cost per
respondent
type
Hours per
respondent
Total all
hours
Total all
costs
US Based USDA Certifying Agents ................................................
US Based USDA Certifying Agents—data entry ............................
45
45
$47.87
24.90
109.23
332.55
$5,229.17
8,281.95
4,915.36
14,964.69
$235,312.78
372,687.76
Subtotal U.S.-Based USDA Certifying Agents ........................
45
....................
441.78
13,511.12
19,880.05
608,000.54
Foreign-Based USDA Certifying Agents .........................................
Foreign-Based USDA Certifying Agents—data entry .....................
30
30
34.40
17.90
653.80
346.64
22,493.03
6,203.93
19,614.07
10,399.19
674,791.04
186,118.00
Subtotal Foreign-Based USDA Certifying Agents ...................
30
....................
1,000.44
28,696.97
30,013.26
860,909.04
Total USDA Accredited Certifying Agents ......................................
75
....................
........................
42,208.09
49,893.31
1,468,909.58
Foreign (Non-USDA) Accredited Certifying Agents ........................
All Certifying Agents ........................................................................
30
105
34.40
....................
614.17
........................
21,129.51
........................
18,425.07
68,318.38
633,885.38
2,102,794.96
For foreign-based USDA-accredited
certifying agents, AMS estimates the
annual cost per certifying agent will be
$28,697 per year. This cost is based on
an estimated 653.80 labor hours for staff
with certification review and procedure
writing responsibilities at $34.40 per
labor hour, including 34.63% benefits,
for a total salary component of $22,493
per foreign-based USDA-accredited
certifying agent per year. These
estimated costs primarily pertain to the
issuance and review of NOP Import
Certificates. The estimated cost for
foreign-based USDA-accredited
certifying agents also includes 346.64
labor hours per certifying agent per year
for administrative support staff to
upload data about certified operations to
OID at $17.90 per labor hour, including
34.63% benefits, for a total salary
component of $6,204 per year.84 85
AMS estimates the annual collection
cost for all foreign-based USDA
accredited certifying agents will total
$860,909. This cost is based on a total
of 19,614.07 hours for all staff with
certification review responsibilities at
$24.90 per labor hour, including 34.63%
benefits, for a total salary component of
$674,791 for staff with certification
review and procedure writing
responsibilities of all foreign-based
USDA-accredited certifying agents. The
estimated cost for all foreign-based
USDA-accredited certifying agents also
includes 10,399.19 hours total hours for
administrative support staff uploading
data about certified operations to OID at
$17.90 per labor hour, including 34.63%
79 Ten hours of training are accounted for in the
2020 Information Collections Renewal for the NOP
(AMS–NOP–19–0090; OMB Control Number: 0581–
0191). Our internal onsite accreditation audit
checklist used by our accreditation audit team
includes a question on training. With the
implementation of this rule, the specific hours of
training offered by our 75 certifying agents will be
documented.
80 The US Bureau of Labor and Statistics reports
that the average separation rate (which captures
both labor force exits and transfers in occupation)
for agricultural inspectors is 14 percent. https://
www.bls.gov/news.release/jolts.t16.htm.
81 In this assessment, all domestic labor rates are
sourced from the U.S. Bureau of Labor Statistics
National Compensation Survey, Occupational
Employment and Wages, May 2020: https://
www.bls.gov/oes/current/oes_nat.htm. Domestic
benefits are based on a Bureau of Labor Statistics
News Release on Employer Costs for Employee
Compensation, which states that benefits account
for 31.7% of total average employer compensation
costs, December 17, 2020.
82 The labor rate for certification review staff is
based on Occupational Employment Statistics
group 13–1041, Compliance Officers. Compliance
officers examine, evaluate, and investigate
eligibility for or conformity with laws and
regulations governing contract compliance of
licenses and permits, and perform other compliance
and enforcement inspection and analysis activities
not classified elsewhere. Compliance Officers
(bls.gov).
83 The labor rate for administrative support staff
is based on Occupational Employment Statistics
group 43–9199, Office and Administrative Support
Workers, who support general office work and data
entry functions. Office and Administrative Support
Workers, All Other (bls.gov).
84 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents, which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD. Agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
85 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
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benefits, for a total salary component of
$186,118.86 87
For foreign-accredited certifying
agents (non-USDA accredited), AMS
estimates the annual cost will be
$21,130 per certifying agent. This cost is
based on an estimated 614.17 labor
hours per year for staff to issue and
review NOP Import Certificates, at
$34.40 per labor hour plus 34.63%
benefits. The total for all foreignaccredited certifying agents is estimated
to be $633,885. The cost is based on an
estimated 18,425 total hours for all staff
involved in the issuance and review of
NOP Import Certificates, at $34.40 per
labor hour plus 34.63% benefits. 88 89
The total cost for all certifying
agents—including the 75 USDAaccredited certifying agents, domesticand foreign-based, and the estimated 30
foreign-accredited (non-USDA)
certifying agents who certify operations
that export products to the U.S.—is
$2,102,795. This cost is based on
68,318.38 total hours at their respective
wage rates and benefits to comply with
the rulemaking’s requirements.
Organic Inspectors
Inspectors conduct on-site inspections
of certified operations and operations
applying for certification and report the
findings to the certifying agent.
Inspectors may be independent
contractors or employees of certifying
agents. Certified operations must be
inspected annually, and a certifying
agent may call for additional
inspections or unannounced inspections
on an as-needed basis (§ 205.403(a)).
Any individuals who apply to conduct
inspections of operations will need to
submit information documenting their
qualifications to the certifying agent
(§ 205.504(a)(3)).
Inspectors provide an inspection
report to the certifying agent for each
operation inspected (§ 205.403(e)) but
are not expected to store the record.
Currently, AMS estimates that
inspectors spend 10 hours on average to
complete an inspection report for a full
annual inspection of an organic
operation. The additional unannounced
inspections required by this rulemaking
are likely to be more limited in scope
(such as pasture or dairy surveillance, or
mass-balance and supply chain
traceability audits). AMS projects, on
average, that inspectors will spend 5
hours to complete an inspection report
for an unannounced targeted-scope
inspection. Organic inspectors do not
have recordkeeping obligations;
certifying agents maintain the records of
inspection reports (see Summary Table
2: Inspectors).
SUMMARY TABLE 2—INSPECTORS
Number of
respondents
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Respondent categories
Wages +
benefits
Cost per
respondent
type
Hours per
respondent
Total all
hours
Total all
costs
USDA US based Inspectors ...........................................................
USDA Foreign based inspectors ....................................................
148
102
$30.79
22.13
30.86
31.12
$950.20
688.53
4,567.17
3,173.80
$140,629.94
70,229.73
All USDA Inspectors ................................................................
250
....................
........................
........................
7,740.97
210,859.67
According to the International
Organic Inspectors Association (IOIA),
there are approximately 250 inspectors
currently inspecting crop, livestock,
handling, and/or wild crop operations
that are certified or have applied for
certification. To comply with this
rulemaking, AMS estimates that 14
percent, or 35, new inspectors with less
than one year of experience must
complete 40 hours of training in their
first year in addition to the baseline
training requirement of 10 hours
annually already accounted for in the
overall program ICR (0191).90 91
AMS estimates that 148 inspectors are
working for USDA-accredited certifying
agents in the United States. For the
additional training of new inspectors,
and for conducting unannounced
targeted-scope inspections, AMS
estimates the annual paperwork impact
cost per domestic-based inspector is
$950.20. This is based on an estimated
30.86 labor hours per year at $30.79 per
labor hour, including 31.7% benefits.
The total annual cost for all domesticbased inspectors is $140,630. This cost
is based on 4,567 total hours for all
domestic based inspectors at $30.79 per
labor hour, including 31.7% benefits.92
AMS estimates that 102 inspectors are
working for USDA-accredited certifying
agents in foreign countries. AMS
estimates the annual paperwork impact
cost per foreign-based inspector is
$688.53. This estimate is based on an
estimated 31.12 labor hours per year at
$22.13 per labor hour, including 34.63%
benefits for the additional training of
new inspectors and for conducting
unannounced targeted-scope
inspections. This rule does not impose
additional recordkeeping costs for
inspectors. The total annual cost for all
foreign-based inspectors is $70,230 at
$31.12 per labor hour, including 34.63%
benefits. The total annual cost for all
inspectors working for USDA-accredited
certifying agents is $210,860, at their
respective wage rates and benefits.93 94
86 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD. Agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
87 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
88 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD.agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
89 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
90 Ten hours of training are accounted for in the
2020 Information Collections Renewal for the NOP
(AMS–NOP–19–0090; OMB Control Number: 0581–
0191). Our internal onsite accreditation audit
checklist used by our accreditation audit team
includes a question on training. With the
implementation of this rule, the specific hours of
training offered by our 75 certifying agents will be
documented.
91 The US Bureau of Labor and Statistics reports
that the average separation rate (which captures
both labor force exits and transfers in occupation)
for agricultural inspectors is 14 percent. https://
www.bls.gov/news.release/jolts.t16.htm.
92 The labor rate for inspectors is based on
Occupational Employment Statistics group 45–
2011, Agricultural Inspectors. Agricultural
inspectors inspect agricultural commodities,
processing equipment, facilities, and fish and
logging operations to ensure compliance with
regulations and laws governing health, quality, and
safety.
93 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD. Agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
94 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
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Producers and Handlers
Domestic and foreign producers and
handlers seeking organic certification
must submit an OSP that details the
practices and activities specific to their
operation. Once certified, operations are
required to update any changes in their
operation or practices to their certifying
agent at least annually.
Uncertified Handlers. This
rulemaking requires that operations that
facilitate the sale or trade of organic
products—including, but not limited to,
certain brokers, importers, and traders—
obtain organic certification and submit
and maintain an OSP. AMS estimates
that 1,985 domestic 95 and 1,379 foreign-
based 96 operations will need to become
certified as a result of the rule. Traders
and brokers do not farm or manufacture
organic products, so the OSPs for
traders and brokers will address fewer
sections of USDA organic regulations
than OSPs for operations that produce
or manufacture organic products.
Certifying agents customize the format
of the OSP to cover standards applicable
to the operations seeking certification.
Therefore, AMS estimates that
preparation of an initial OSP will
require 40 reporting hours, plus 10
hours of annual recordkeeping. The
estimated annual reporting burden for
each entity to update its OSP in future
3617
years is 20 hours (See Summary Table
3a: Uncertified Handlers).
All operations that export organic
products to the United States must
request an NOP Import Certificate from
their certifying agent. Further,
operations that import organic products
must verify and reconcile each
shipment with its associated NOP
Import Certificate and verify that
organic integrity was maintained
throughout the import process. In
addition, domestic and foreign handlers
that must obtain organic certification as
a result of this rulemaking will also
need to comply with the labeling
requirements for nonretail containers.
SUMMARY TABLE 3a—UNCERTIFIED HANDLERS
Number of
respondents
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Respondent categories
Wages +
benefits
Total
hours per
respondent
Total
cost per
respondent
type
Total all
hours
Total all
costs
Formerly Excluded Handlers—Domestic .......
Formerly Excluded Handlers—Foreign ..........
1,985
1,379
$48.64
34.95
50.97
53.42
$2,478.80
1,867.02
101,166.47
73,660.94
$4,920,414.48
2,574,623.40
All Uncertified Handlers ..........................
3,364
....................
........................
........................
174,827.41
7,495,037.88
AMS estimates the annual paperwork
impact for each domestic handler to
prepare their initial organic system
plan, verify and reconcile imported
shipments with their respective NOP
Import Certificates, and verify that the
organic integrity of the product was
maintained through shipping is
2,478.80. This is based on an estimated
50.97 labor hours at $48.64 per labor
hour, including 31.7% benefits. The
total cost to all previously uncertified
domestic handlers is $4,920,415. This
cost is based on 101,166.47 total labor
hours at $48.64 per labor hour,
including 31.7% benefits.97
AMS estimates the annual paperwork
impact for each foreign-based handler to
prepare their initial organic system plan
and to work with their certifying agent
to prepare NOP Import Certificates for
the products they export is $1,867.02.
This is based on an estimated 53.42
labor hours per year at $34.95 per labor
hour, which includes 34.63% for
benefits. The total cost to all previously
uncertified foreign handlers is
$2,574,623.40. This cost is based on
73,660.94 total labor hours at $34.95 per
labor hour, which includes 34.63% for
benefits. Total costs to the 3,364
previously uncertified handlers,
domestic and foreign, is $7,495,038,
based on 174,827 total labor hours at
their respective domestic and foreign
wage rates and benefits. This cost is to
prepare and keep initial OSPs and
related records, and to prepare, verify,
and reconcile NOP Import Certificates
for compliance.98 99
Certified Operations and New
Applicants under Current Rules. There
currently are 44,725 organic operations
worldwide that are certified to the
USDA organic standards. Over the next
12 months, AMS expects 2,639
operations will seek organic
certification, based on the 5.9% rate of
95 Please refer to the ‘‘Applicability and
Exemptions from Certification (§§ 205.100–101)’’
chapter in the Regulatory Impact Analysis (RIA) for
an explanation of how previously excluded
domestic handlers were estimated.
96 AMS assumes the 1,985 domestic excluded
operations represent 59% of the global total
benchmarked 59%/41% ratio of domestic to foreign
operations and certifying agents. Therefore, AMS
estimate there are an additional 1,379 foreign
formerly excluded operations, for a total of 3,364
new handlers that will need organic certification.
97 For uncertified handlers, AMS chose to use the
same labor rate as certified producers and handlers:
Occupational Employment Statistics group 11–
9013, Farmers, Ranchers, and Other Agricultural
Managers.
98 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents which were 70.3% of
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growth in number of operations
observed in the last 12 months under
current rules. Therefore, AMS estimates
that 27,945 operations based in the
United States, and 19,419 operations
based in foreign countries, including the
respective applicants for certification,
will be impacted by this rulemaking.100
All currently certified organic
operations and projected new applicants
must describe in their OSP their
procedures for monitoring, verifying,
and demonstrating the organic status of
their suppliers and products received to
prevent organic fraud. All certified
organic operations must also comply
with revised nonretail container
labeling requirements and must
maintain all records about their organic
production and/or handling for five
years (§ 205.103(b)(3)).
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD.agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
99 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
100 Organic Integrity Database: https://
organic.ams.usda.gov/integrity/.
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In addition, AMS estimates a one-time
paperwork burden of 11,800 hours for
5,900 producer group operations to
prepare a detailed Internal Control
System (ICS) for their OSP, including
procedures to address conflicts of
interest and manage the unique
challenges of producer group oversight.
In addition, training requirements for
ICS personnel and producer group
members are expanded to 29,500 hours
annually (§§ 205.201, 205.400(g) and
205.403).101
SUMMARY TABLE 3b—CERTIFIED ORGANIC OPERATIONS AND NEW APPLICANTS
Number of
respondents
Respondent categories
Total cost/
respondent
type
Total hours/
respondent
Total
all hours
Total
all costs
Certified Producers & Handlers—New and Existing Domestic ......
Certified Producers & Handlers—New and Existing Foreign .........
27,945
19,419
$48.64
34.95
1.67
3.44
$81.07
120.39
46,579.60
66,888.32
$2,265,483.08
2,337,904.67
All New and Existing Producers & Handlers ..................................
47,364
....................
........................
........................
113,467.92
4,603,388.08
The U.S. government, including the
USDA and the U.S. Trade
Representative, work closely together to
implement processes that determine the
equivalence of foreign organic
certification programs and then
negotiate an arrangement or agreement
as appropriate.105 Formerly, the organic
regulations only addressed this
authority in general terms under
§ 205.500(c) but did not describe the
criteria, scope, and other parameters to
establish, oversee, or terminate such
arrangements or agreements. The
rulemaking describes equivalence
determinations in more detail; this
creates a new type of PRA respondent
category. The rulemaking allows an
equivalence determination if the U.S.
government determines that the
technical requirements and conformity
assessment system under which foreign
products labeled as organic are
produced and handled are at least
equivalent to the requirements of the
OFPA and the USDA organic
regulations. The rulemaking requires
periodic assessment.
AMS expects these periodic peer
review assessments will be similar in
depth and frequency to the audits of
USDA-accredited certifying agents and
estimates a comparable level of
reporting and recordkeeping burden by
foreign governments with which USDA
has negotiated trade arrangements or
agreements. AMS estimates the
collection cost for the periodic review of
a single foreign government is $602.
This cost is based on 7.5 reporting labor
hours averaged as needed and an
estimated 10 hours of annual
recordkeeping per foreign government
per year at $24.59 per labor hour,
including 34.63% benefits, for a total
salary component of $602.06 per year
reviewed. The total cost for foreign
governments to be assessed for a trade
arrangement or agreement is $4,816.
This cost is averaged as 140 total labor
hours for all foreign governments at
$24.59 per labor hour, including 34.63%
benefits. 106 107
Total (Domestic and Foreign)
Information Collection Cost (Reporting
and Recordkeeping) of Rulemaking:
$14,416,897 (Also, see Summary Table
4: All Reporting and Recordkeeping
Hours and Costs, and All Domestic
Reporting and Recordkeeping Hours
and Costs).
Total All Reporting Burden Cost:
$12,454,097.
Estimate of Burden: Public reporting
burden for the collection of information
is estimated to average 0.56 hours per
year per response.
Respondents: Certifying agents,
certified operations, inspectors, and
foreign governments.
Estimated Number of Reporting
Respondents: 51,091.
Estimated Number of Reporting
Responses: 566,387.
Estimated Total Annual Burden on
Reporting Respondents: 318,859 hours.
Estimated Total Annual Reporting
Responses per Reporting Respondents:
11.09 reporting responses per reporting
respondents.
Total All Recordkeeping Burden Cost:
$1,962,800.
Estimate of Burden: Public
recordkeeping burden is estimated to be
101 Meinshausen F., Richter, T., Blockeel, J., and
Huber, B., Group Certification: Internal Control
Systems in Organic Agriculture: Significance,
Opportunities and Challenges, Research Institute of
Organic Agriculture FiBL, March 2019.
102 The labor rate for producers and handlers is
based on Occupational Employment Statistics
group 11–9013, Farmers, Ranchers, and Other
Agricultural Managers, who plan, direct, or
coordinate the management or operation of farms,
ranches, or other agricultural establishments.
103 The source of the data is based on average
World Bank wage rates for countries with USDA-
accredited certifying agents which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD. Agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
104 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
105 The United States currently has organic trade
arrangements with Canada, the European Union,
the United Kingdom, Israel, Japan, New Zealand,
South Korea, Taiwan, and Switzerland.
106 The source of the data is based on average
World Bank wage rates for countries with USDAaccredited certifying agents which were 70.3% of
U.S. labor rates in 2020. https://data.worldbank.org/
indicator/NY.GDP.PCAP.PP.CD. Agents: https://
stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
107 Benefits are based on a review of data from the
Organisation for Economic Co-Operation and
Development (OECD), which indicates that benefits
account for 34.63% of total compensation in foreign
countries with USDA-accredited certifying agents.
AMS estimates that the average
annual paperwork impact for domestic
USDA-certified organic producers and
handlers to develop fraud prevention
procedures and to comply with
nonretail container labeling
requirements is $81.07. This is based on
an estimated 1.67 labor hours at $48.64
per labor hour, including 31.7%
benefits. The total cost for all domestic
certified organic producers and handlers
to comply with these new requirements
is $2,265,483.08. This cost is based on
46,579.60 labor hours at $48.64 per
labor hour, including 31.7% benefits.102
AMS estimates the average annual
paperwork impact for foreign-based
USDA-certified organic producers and
handers to create fraud prevention
procedures and to comply with
nonretail container labeling
requirements is $120.39. This is based
on an estimated 3.44 labor hours per
year at $34.95 per labor hour, including
34.63% benefits. The total cost for all
foreign producers and handlers certified
to the USDA organic standards is
$2,337,904.67. This cost is based on
66,888.32 labor hours year at $34.95 per
labor hour, including 34.63% benefits.
The total cost for the 47,364 current and
projected certified organic producers
and handlers, domestic and foreign, is
$4,603,388. This cost is based on
113,4677.92 labor hours at their
respective domestic and foreign wages
and benefits.103 104
Foreign Governments
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benefits
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an annual total of 0.90 hours per year
per respondent.
Respondents: Certifying agents,
certified operations, and foreign
governments.
Estimated Number of Recordkeeping
Respondents: 50,811.
Estimated Total Recordkeeping
Burden on Respondents: 45,636 hours.
Estimated Total Recordkeeping
Responses per Recordkeeping
Respondents: 1 recordkeeping response
per recordkeeping respondents.
Total Domestic Only Information
Collection Cost (Reporting and
Recordkeeping) of Rulemaking:
$7,934,528.
Total Domestic Only Reporting
Burden Cost: $6,627,301.
Estimate of Burden: Public domestic
only reporting burden is estimated to be
an annual total 0.43 hours per year per
domestic respondent.
Respondents: Certifying agents,
certified operations, and inspectors.
Estimated Number of Domestic
Reporting Respondents: 30,123.
Estimated Number of Domestic
Reporting Responses: 334,168.
Estimated Total Annual Reporting
Burden on Domestic Respondents:
145,315 hours.
Estimated Total Domestic Reporting
Responses per Reporting Respondents:
11.09 reporting response per reporting
respondents.
Total Domestic Only Recordkeeping
Burden Cost: $1,307,227.
3619
Estimate of Burden: Public domestic
only recordkeeping burden is estimated
to be an annual total of 1 hours per year
per respondent.
Respondents: Certifying agents and
certified operations.
Estimated Number of Domestic
Recordkeeping Respondents: 29,975.
Estimated Total Annual
Recordkeeping Burden on Domestic
Respondents: 26,878 hours.
Estimated Number of Domestic
Recordkeeping Responses: 29,929.
Estimated Total Domestic
Recordkeeping Responses per
Recordkeeping Respondents: 1
recordkeeping response per
recordkeeping respondents.
SUMMARY TABLE 4—ALL HOURS AND COSTS, ALL DOMESTIC HOURS AND COSTS, AND ALL FOREIGN HOURS AND COSTS
Hours
Number of
respondents
Respondent types
Total for All (Reporting & Recordkeeping) ....
364,495
$14,416,897
51,091
All Reporting ...........................................
318,859
12,454,097
51,091
All Recordkeeping ...................................
45,636
1,962,800
50,811
Certifying agents, certified operations, inspectors, and foreign governments.
Certifying agents, certified operations, inspectors, and foreign governments.
Certifying agents, certified operations, and foreign governments.
Just Domestic—All (Reporting & Recordkeeping).
Just Domestic Reporting ........................
Just Domestic Recordkeeping ................
172,193
7,934,528
30,123
Certifying agents, certified operations, and inspectors.
145,315
26,878
6,627,301
1,307,227
30,123
29,975
Certifying agents, certified operations, and inspectors.
Certifying agents and certified operations.
Certifying agents, certified operations, inspectors, and foreign governments.
Certifying agents, certified operations, inspectors, and foreign governments.
Certifying agents, certified operations, and foreign governments.
Just Foreign—All (Reporting & Recordkeeping).
Just Foreign Reporting ...........................
192,301
6,482,369
20,968
173,543
5,826,795
20,968
Just Foreign Recordkeeping ...................
18,758
655,573
20,836
E. Executive Order 13175
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Costs
Executive Order 13175 requires
Federal agencies to consult and
coordinate with Tribes on a
government-to-government basis on
policies that have Tribal implications,
including regulations, legislative
comments, or proposed legislation.
Additionally, other policy statements or
actions that have substantial direct
effects on one or more Indian Tribes, the
relationship between the Federal
Government and Indian Tribes, or on
the distribution of power and
responsibilities between the Federal
Government and Indian Tribes also
require consultation.
AMS hosted a virtual tribal listening
session on April 9, 2020, to discuss the
Strengthening Organic Enforcement
proposed rule and upcoming public
comment opportunity. AMS has not
received comments from Tribes during
the rulemaking process. AMS conducted
an analysis of possible Tribal impacts
and determined that any impact is most
likely to be positive. AMS finds
oversight protections and fraud
deterrence actions that will have
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positive benefits for organic producers
extend to any Tribal organic producers.
Further, the specific provisions related
to grower groups may benefit small
producers in a Tribe who wish to join
together under a shared certification for
market development purposes.
If a tribe requests consultation in the
future, AMS will work with the Office
of Tribal Relations to ensure meaningful
consultation is provided. AMS also
stands ready to provide technical
assistance to Tribes and operators
wishing to participate in the organic
certification process.
E.O. 13132. The rule does not impose
substantial direct costs or effects on
States, does not alter the relationship
between States and the federal
government, and does not alter the
distribution of powers and
responsibilities among the various
levels of government. States had the
opportunity to comment on the
proposed rule. No States provided
public comment on the federalism
implications of this rule. Therefore,
AMS has concluded that this
rulemaking does not have federalism
implications.
F. Executive Order 13132
Executive Order 13132 mandates that
federal agencies consider how their
policymaking and regulatory activities
impact the policymaking discretion of
States and local officials and how well
such efforts conform to the principles of
federalism defined in said order. This
executive order only pertains to
regulations with clear federalism
implications.
AMS has determined that this
rulemaking conforms with the
principles of federalism described in
G. Civil Rights Impact Analysis
AMS has reviewed this rulemaking in
accordance with the Department
Regulation 4300–4, Civil Rights Impact
Analysis, to address any major civil
rights impacts the rule might have on
minorities, women, and persons with
disabilities. After a careful review of the
rule’s intent and provisions, AMS
determined that this rule will affect
certifying agents and organic inspectors,
handlers of organic products, and
organic producers. AMS also
determined that this rule has no
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potential for affecting producers,
handlers, certifying agents, or inspectors
in protected groups differently than the
general population of producers,
handlers, certifying agents, or
inspectors.
Protected individuals have the same
opportunity to participate in NOP as
non-protected individuals. The USDA
organic regulations prohibit
discrimination by certifying agents.
Specifically, § 205.501(d) of the current
regulations for accreditation of
certifying agents provides that ‘‘No
private or governmental entity
accredited as a certifying agent under
this subpart shall exclude from
participation in or deny the benefits of
NOP to any person due to
discrimination because of race, color,
national origin, gender, religion, age,
disability, political beliefs, sexual
orientation, or marital or family status.’’
Section 205.501(a)(2) requires
‘‘certifying agents to demonstrate the
ability to fully comply with the
requirements for accreditation set forth
in this subpart’’ including the
prohibition on discrimination. The
granting of accreditation to certifying
agents under § 205.506 requires the
review of information submitted by the
certifying agent and an on-site review of
the certifying agent’s client operation.
Further, if certification is denied,
§ 205.405(d) requires that the certifying
agent notify the applicant of their right
to file an appeal to the AMS
Administrator in accordance with
§ 205.681.
These regulations provide protections
against discrimination, thereby
permitting all producers, regardless of
race, color, national origin, gender,
religion, age, disability, political beliefs,
sexual orientation, or marital or family
status, who voluntarily choose to adhere
to the rule and qualify, to be certified as
meeting NOP requirements by an
accredited certifying agent. This action
in no way changes any of these
protections against discrimination.
H. Related Documents
Documents related to this rule include
the Organic Foods Production Act of
1990, as amended, (7 U.S.C. 6501–6524)
and its implementing regulations (7 CFR
part 205). On August 5, 2020, AMS
published the proposed rule (85 FR
47536) to notify the public of and
request comments on the potential
changes to the organic regulations
discussed in this rulemaking.
List of Subjects in 7 CFR Part 205
Administrative practice and
procedure, Agricultrual Commodities,
Agriculture, Animals, Archives and
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records, Fees, Imports, Labeling,
Livestock, Organically produced
products, Plants, Reporting and
recordkeeping requirements, Seals and
insignia, Soil conservation.
For the reasons set forth in the
preamble, the Agricultural Marketing
Service amends 7 CFR part 205 as
follows:
PART 205—NATIONAL ORGANIC
PROGRAM
1. The authority citation for part 205
continues to read as follows:
■
Authority: 7 U.S.C. 6501–6524.
2. Section 205.2 is amended by:
a. Adding in alphabetical order the
terms ‘‘Adverse action’’, ‘‘Certification
activity’’, ‘‘Certification office’’,
‘‘Certification review’’, and ‘‘Conformity
assessment system’’;
■ b. Revising the terms ‘‘Handle’’,
‘‘Handler’’, and ‘‘Handling operation’’;
■ c. Adding in alphabetical order the
terms ‘‘Internal control system’’,
‘‘Organic exporter’’, ‘‘Organic fraud’’,
‘‘Organic importer’’, ‘‘Organic Integrity
Database’’, ‘‘Producer group member’’,
‘‘Producer group operation’’, ‘‘Producer
group production unit’’, and ‘‘Retail
establishment’’;
■ d. Removing the terms ‘‘Retail food
establishment’’; and
■ e. Adding in alphabetical order the
terms ‘‘Supply chain traceability audit’’,
‘‘Technical requirements’’, and
‘‘Unannounced inspection’’.
The revisions and additions read as
follows:
■
■
§ 205.2
Terms defined.
*
*
*
*
*
Adverse action. A noncompliance
decision that adversely affects
certification, accreditation, or a person
subject to the Act, including a proposed
suspension or revocation; a denial of
certification, accreditation, or
reinstatement; a cease and desist notice;
or a civil penalty.
*
*
*
*
*
Certification activity. Any business
conducted by a certifying agent, or by a
person acting on behalf of a certifying
agent, including but not limited to:
certification management;
administration; application review;
inspection planning; inspections;
sampling; inspection report review;
material review; label review; records
retention; compliance review;
investigating complaints and taking
adverse actions; certification decisions;
and issuing transaction certificates.
Certification office. Any site or facility
where certification activities are
conducted, except for certification
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activities that occur at certified
operations or applicants for
certification, such as inspections and
sampling.
*
*
*
*
*
Certification review. The act of
reviewing and evaluating a certified
operation or applicant for certification
and determining compliance or ability
to comply with the USDA organic
regulations. This does not include
performing an inspection.
*
*
*
*
*
Conformity assessment system. All
activities, including oversight,
accreditation, compliance review, and
enforcement, undertaken by a
government to ensure that the
applicable technical requirements for
the production and handling of organic
agricultural products are fully and
consistently applied.
*
*
*
*
*
Handle. To sell, process, or package
agricultural products, including but not
limited to trading, facilitating sale or
trade on behalf of a seller or oneself,
importing to the United States,
exporting for sale in the United States,
combining, aggregating, culling,
conditioning, treating, packing,
containerizing, repackaging, labeling,
storing, receiving, or loading.
Handler. Any person that handles
agricultural products, except final
retailers of agricultural products that do
not process agricultural products.
Handling operation. Any operation
that handles agricultural products,
except final retailers of agricultural
products that do not process agricultural
products.
*
*
*
*
*
Internal control system. An internal
quality management system that
establishes and governs the review,
monitoring, training, and inspection of
the producer group operation, and the
procurement and distribution of shared
production and handling inputs and
resources, to maintain compliance with
the USDA organic regulations.
*
*
*
*
*
Organic exporter. The final certified
exporter of the organic agricultural
product, who facilitates the trade of,
consigns, or arranges for the transport/
shipping of the organic agricultural
product from a foreign country to the
United States.
Organic fraud. Deceptive
representation, sale, or labeling of
nonorganic agricultural products or
ingredients as ‘‘100 percent organic,’’
‘‘organic,’’ or ‘‘made with organic
(specified ingredients or food
group(s)).’’
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Organic importer. The operation
responsible for accepting imported
organic agricultural products within the
United States and ensuring NOP Import
Certificate data are entered into the U.S.
Customs and Border Protection import
system of record.
Organic Integrity Database. The
National Organic Program’s electronic,
web-based reporting tool for the
submission of data, completion of
certificates of organic operation, and
other information, or the tool’s
successors.
*
*
*
*
*
Producer group member. An
individual engaged in the activity of
producing or harvesting agricultural
products as a member of a producer
group operation.
Producer group operation. A
producer, organized as a person,
consisting of producer group members
and production units in geographic
proximity governed by an internal
control system under one organic
system plan and certification.
Producer group production unit. A
defined subgroup of producer group
members in geographic proximity
within a single producer group
operation that use shared practices and
resources to produce similar agricultural
products.
*
*
*
*
*
Retail establishment. Restaurants,
delicatessens, bakeries, grocery stores,
or any retail business with a restaurant,
delicatessen, bakery, salad bar, bulk
food self-service station, or other eat-in,
carry-out, mail-order, or delivery service
of raw or processed agricultural
products.
*
*
*
*
*
Supply chain traceability audit. The
process of identifying and tracking the
movement, sale, custody, handling, and
organic status of an agricultural product
along a supply chain to verify the
agricultural product’s compliance with
this part.
*
*
*
*
*
Technical requirements. A system of
relevant laws, regulations, regulatory
practices, standards, policies, and
procedures that address the
certification, production, and handling
of organic agricultural products.
*
*
*
*
*
Unannounced inspection. The act of
examining and evaluating all or a
portion of the production or handling
activities of a certified operation
without advance notice to determine
compliance with the Act and the
regulations in this part.
*
*
*
*
*
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3. Section 205.100 is amended by
revising paragraph (a) and paragraph (c)
introductory text to read as follows:
■
§ 205.100
What has to be certified.
(a) Except for the exempt operations
described in § 205.101, each operation
or portion of an operation that produces
or handles agricultural products
intended to be sold, labeled, or
represented as ‘‘100 percent organic,’’
‘‘organic,’’ or ‘‘made with organic
(specified ingredients or food group(s))’’
must be certified according to the
provisions of subpart E of this part and
must meet all other applicable
requirements of this part.
*
*
*
*
*
(c) Any person or responsibly
connected person that:
*
*
*
*
*
■ 4. Revise § 205.101 to read as follows:
§ 205.101
Exemptions from certification.
The following operations in
paragraphs (a) through (h) of this section
are exempt from certification under
subpart E of this part and from
submitting an organic system plan for
acceptance or approval under § 205.201
but must comply with the applicable
organic production and handling
requirements of subpart C of this part,
the applicable labeling requirements of
subpart D of this part, and any
requirements described in paragraphs
(a) through (i) of this section.
(a) A production or handling
operation that sells agricultural
products as ‘‘organic’’ but whose gross
agricultural income from organic sales
totals $5,000 or less annually.
(b) A retail establishment that does
not process organically produced
agricultural products.
(c) A retail establishment that
processes, at the point of final sale,
agricultural products certified under
this part as ‘‘100 percent organic,’’
‘‘organic,’’ or ‘‘made with organic
(specified ingredients or food
group(s)).’’
(d) A handling operation that only
handles agricultural products that
contain less than 70 percent organic
ingredients (as described in
§ 205.301(d)) or that only identifies
organic ingredients on the information
panel.
(e) An operation that only receives,
stores, and/or prepares for shipment,
but does not otherwise handle, organic
agricultural products that:
(1) Are enclosed in sealed, tamperevident packages or containers prior to
being received or acquired by the
operation; and
(2) Remain in the same sealed,
tamper-evident packages or containers
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3621
and are not otherwise handled while in
the control of the operation.
(f) An operation that only buys, sells,
receives, stores, and/or prepares for
shipment, but does not otherwise
handle, organic agricultural products
already labeled for retail sale that:
(1) Are enclosed in sealed, tamperevident packages or containers that are
labeled for retail sale prior to being
received or acquired by the operation;
and
(2) Remain in the same sealed,
tamper-evident packages or containers
that are labeled for retail sale and are
not otherwise handled while in the
control of the operation.
(g) A Customs broker (per 19 CFR
111.1) that only conducts customs
business but does not otherwise handle
organic agricultural products.
(h) An operation that only arranges for
the shipping, storing, transport, or
movement of organic agricultural
products but does not otherwise handle
organic products.
(i) Recordkeeping by exempt
operations.
(1) Exempt operations described in
paragraphs (a) and (c) through (f) of this
section must make available to
representatives of the Secretary, upon
request, records that:
(i) Demonstrate that agricultural
products identified as organic were
organically produced and handled; and
(ii) Verify quantities of organic
agricultural products received and
shipped or sold
(2) All records described in this
section must be maintained for no less
than 3 years beyond their creation, and
the operations must allow
representatives of the Secretary and the
applicable State organic programs’
governing State official access to these
records for inspection and copying
during normal business hours to
determine compliance with the
applicable regulations set forth in this
part.
■ 5. Section 205.103 is amended by:
■ a. Revising paragraph (b)(2);
■ b. Redesignating paragraphs (b)(3) and
(4) as paragraphs (b)(4) and (5); and
■ c. Adding new paragraph (b)(3).
The revision and addition read as
follows:
§ 205.103 Recordkeeping by certified
operations.
*
*
*
*
*
(b) * * *
(2) Fully disclose all activities and
transactions of the certified operation,
in sufficient detail as to be readily
understood and audited; records must
span the time of purchase or
acquisition, through production, to sale
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or transport and be traceable back to the
last certified operation;
(3) Include audit trail documentation
for agricultural products handled or
produced by the certified operation and
identify agricultural products on these
records as ‘‘100% organic,’’ ‘‘organic,’’
or ‘‘made with organic (specified
ingredients or food group(s)),’’ or similar
terms, as applicable;
*
*
*
*
*
■ 6. Section 205.201 is amended by:
■ a. Removing the words ‘‘or excluded’’
in paragraph (a) introductory text;
■ b. Revising paragraph (a)(3); and
■ c. Adding paragraph (c).
The revision and addition to read as
follows:
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§ 205.201 Organic production and
handling system plan.
(a) * * *
(3) A description of the monitoring
practices and procedures to be
performed and maintained, including
the frequency with which they will be
performed, to verify that the plan is
effectively implemented. This must
include a description of the monitoring
practices and procedures to verify
suppliers in the supply chain and
organic status of agricultural products
received, and to prevent organic fraud,
as appropriate to the certified
operation’s activities, scope, and
complexity;
*
*
*
*
*
(c) In addition to paragraph (a) of this
section, a producer group operation’s
organic system plan must describe its
internal control system. The description
of the internal control system must:
(1) Define the organizational
structure, roles, and responsibilities of
all personnel;
(2) Identify producer group
production units and locations;
(3) Describe measures to protect
against potential conflicts of interest
and protect internal control system
personnel from retribution;
(4) Define geographic proximity
criteria for producer group members and
producer group production units;
(5) Describe procedures for accepting
new members into the producer group
operation, including initial inspection
and compliance determination;
(6) Describe characteristics of highrisk producer group members and
producer group production units;
(7) Describe how shared resources,
including production practices and
inputs, are procured and provided to all
producer group members and personnel;
(8) Describe how training, education,
and technical assistance is provided to
producer group members and internal
control system personnel;
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(9) Describe the system of records
used to demonstrate compliance with
this part, including traceability and
mass-balance audits; and
(10) Describe how internal
monitoring, surveillance, inspection,
sanctions, and auditing are used to
assess the compliance of all producer
group members.
■ 7. Add § 205.273 to subpart C to read
as follows:
§ 205.273
Imports to the United States.
Each shipment of organic agricultural
products imported into the United
States must be certified pursuant to
subpart E of this part, labeled pursuant
to subpart D of this part, be declared as
organic to U.S. Customs and Border
Protection, and be associated with valid
NOP Import Certificate data.
(a) Persons exporting organic
agricultural products to the United
States must request an NOP Import
Certificate from a certifying agent prior
to their export. Only certifying agents
accredited by the USDA or foreign
certifying agents authorized under an
organic trade arrangement or agreement
may issue an NOP Import Certificate.
(b) The certifying agent must review
an NOP Import Certificate request and
determine whether the export complies
with the USDA organic regulations. The
certifying agent must have and
implement a documented organic
control system for intaking and
approving or rejecting the validity of an
NOP Import Certificate request. The
certifying agent shall issue the NOP
Import Certificate through the Organic
Integrity Database only if the export
complies with the USDA organic
regulations.
(c) Each compliant organic import
must be declared as organic to U.S.
Customs and Border Protection by
entering NOP Import Certificate data
into the U.S. Customs and Border
Protection’s Automated Commercial
Environment system. Organic imports
must be clearly identified and marked
as organic on all import documents
including but not limited to invoices,
packing lists, bills of lading, and U.S.
Customs and Border Protection entry
data. Only NOP Import Certificate data
generated by the Organic Integrity
Database are valid.
(d) Upon receiving a shipment with
organic agricultural products, the
organic importer must ensure the import
is accompanied by accurate NOP Import
Certificate data and must verify that the
shipment has had no contact with
prohibited substances pursuant to
§ 205.272 or exposure to ionizing
radiation pursuant to § 205.105, since
export. The organic importer must have
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a documented organic control system to
conduct this verification.
■ 8. Amend § 205.300 by revising
paragraph (c) to read as follows:
§ 205.300
Use of the term, ‘‘organic.’’
*
*
*
*
*
(c) Products produced in a foreign
country and exported for sale in the
United States must be certified pursuant
to subpart E of this part, labeled
pursuant to this subpart D, and must
comply with the requirements in
§ 205.273.
*
*
*
*
*
■ 9. Amend § 205.301 by revising
paragraphs (f)(2) and (3) to read as
follows:
§ 205.301
Product composition.
*
*
*
*
*
(f) * * *
(2) Be processed using ionizing
radiation, pursuant to § 205.105(f);
(3) Be produced using sewage sludge,
pursuant to § 205.105(g);
*
*
*
*
*
■ 10. Amend § 205.302 by revising
paragraphs (a)(1) through (3) to read as
follows:
§ 205.302 Calculating the percentage of
organically produced ingredients.
(a) * * *
(1) Dividing the total net weight of the
combined organic ingredients at
formulation by the total weight of all
ingredients of the product at
formulation. Water and salt added as
ingredients at formulation are excluded
from the calculation.
(2) Dividing the total fluid volume of
the combined organic ingredients at
formulation by the total fluid volume of
all ingredients of the product at
formulation if the product and
ingredients are liquid. Water and salt
added as ingredients at formulation are
excluded from the calculation. If the
liquid product is identified on the
principal display panel or information
panel as being reconstituted from
concentrates, the calculation should be
made based on single-strength
concentrations of all ingredients.
(3) For products containing
organically produced ingredients in
both solid and liquid form, dividing the
combined net weight of the solid
organic ingredients and the net weight
of the liquid organic ingredients at
formulation by the total weight of all
ingredients of the product at
formulation. Water and salt added as
ingredients at formulation are excluded
from the calculation.
*
*
*
*
*
■ 11. Revise § 205.307 to read as
follows:
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§ 205.307
Labeling of nonretail containers.
(a) Nonretail containers used to ship
or store certified organic agricultural
products must display:
(1) Identification of the product as
organic; and
(2) The production lot number,
shipping identification, or other unique
information that links the container to
audit trail documentation.
(b) Audit trail documentation for
nonretail containers must identify the
last certified operation that handled the
agricultural product.
(c) Paragraph (a)(1) of this section
does not apply to nonretail containers
used to ship or store agricultural
products packaged for retail sale with
organic identification visible on the
retail label.
(d) Shipping containers of
domestically produced product labeled
as organic intended for export to
international markets may be labeled in
accordance with any shipping container
labeling requirements of the foreign
country of destination or the container
labeling specifications of a foreign
contract buyer: Provided, that, the
shipping containers and shipping
documents accompanying such organic
products are clearly marked ‘‘For Export
Only’’ and: Provided further, that proof
of such container marking and export
must be maintained by the handler in
accordance with recordkeeping
requirements for exempt operations
under § 205.101.
■ 12. Section 205.310 is amended by
revising the section heading and
paragraphs (a) and (b) to read as follows:
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§ 205.310 Agricultural products produced
or processed by an exempt operation.
(a) An agricultural product
organically produced or processed by an
exempt operation must not:
(1) Display the USDA seal or any
certifying agent’s seal or other
identifying mark which represents the
exempt operation as a certified organic
operation; or
(2) Be represented as a certified
organic product or certified organic
ingredient to any buyer.
(b) An agricultural product
organically produced or processed by an
exempt operation may be identified as
an organic product or organic ingredient
in a multi-ingredient product produced
by the exempt operation. Such product
or ingredient must not be identified or
represented as ‘‘organic’’ in a product
processed by others.
*
*
*
*
*
■ 13. Section 205.400 is amended by:
■ a. Removing ‘‘§ 205.200’’ and adding
in its place ‘‘§ 205.201’’ in paragraph
(b); and
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■
b. Adding paragraph (g).
The addition reads as follows:
§ 205.400 General requirements for
certification.
*
*
*
*
*
(g) In addition to paragraphs (a)
through (f) of this section, a producer
group operation must:
(1) Be organized as a person;
(2) Use centralized processing,
distribution, and marketing facilities
and systems;
(3) Be organized into producer group
production units;
(4) Maintain an internal control
system to implement the practices
described in § 205.201(c) and ensure
compliance with this part;
(5) Ensure that all agricultural
products sold, labeled, or represented as
organic are produced only by producer
group members using land and facilities
within the certified operation;
(6) Ensure that producer group
members do not sell, label, or represent
their agricultural products as organic
outside of the producer group operation
unless they are individually certified;
(7) Report to the certifying agent, at
least annually, the name and location of
all producer group members and
producer group production units, the
agricultural products produced,
estimated yields, and size of production
areas;
(8) Conduct internal inspections of
each producer group member, at least
annually, by internal inspectors with
the member present, which must
include mass-balance audits and
reconciliation of each producer group
member’s and each producer group
production unit’s yield and group sales;
(9) Implement recordkeeping
requirements to ensure traceability from
production at each producer group
member and production unit through
handling to sale and transport;
(10) Implement procedures to ensure
all production and handling by the
producer group operation is compliant
with the USDA organic regulations and
the Act; and
(11) Address any other terms or
conditions determined by the
Administrator to be necessary to enforce
compliance with the USDA organic
regulations and the Act.
§ 205.401
[Amended]
14. Amend § 205.401 in paragraph (a)
by removing ‘‘§ 205.200’’ and adding in
its place ‘‘§ 205.201’’.
■ 15. Section 205.403 is amended by:
■ a. Redesignating paragraph (a)(2) as
paragraph (a)(3);
■ b. Adding new paragraph (a)(2);
■ c. Redesignating paragraphs (b)
through (e) as paragraphs (c) through (f);
■
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3623
d. Adding new paragraph (b);
e. In newly redesignated paragraph
(d)(2), removing ‘‘§ 205.200’’ and
adding in its place ‘‘§ 205.201’’; and
■ f. Adding paragraphs (d)(4) and (5).
The additions read as follows:
■
■
§ 205.403
On-site inspections.
(a) * * *
(2) Inspections of a producer group
operation must:
(i) Assess the internal control system’s
compliance, or ability to comply, with
the requirements of § 205.400(g)(8). This
must include review of the internal
inspections conducted by the internal
control system.
(ii) Conduct witness audits of internal
control system inspectors performing
inspections of the producer group
operation.
(iii) Individually inspect at least 1.4
times the square root or 2% of the total
number of producer group members,
whichever is higher. All producer group
members determined to be high risk by
the certifying agent must be inspected.
At least one producer group member in
each producer group production unit
must be inspected.
(iv) Inspect each handling facility.
*
*
*
*
*
(b) Unannounced inspections. (1) A
certifying agent must, on an annual
basis, conduct unannounced
inspections of a minimum of five
percent of the operations it certifies,
rounded up to the nearest whole
number.
(2) Certifying agents must be able to
conduct unannounced inspections of
any operation they certify and must not
accept applications or continue
certification with operations located in
areas where they are unable to conduct
unannounced inspections.
*
*
*
*
*
(d) * * *
(4) Mass-balances, in that quantities of
organic product and ingredients
produced or purchased account for
organic product and ingredients used,
stored, sold, or transported (that is,
inputs account for outputs); and
(5) That organic products and
ingredients are traceable by the
operation from the time of purchase or
acquisition through production to sale
or transport; and that the certifying
agent can verify compliance back to the
last certified operation.
*
*
*
*
*
■ 16. Section § 205.404 is amended by
revising paragraph (b), redesignating
paragraph (c) as paragraph (d), and
adding a new paragraph (c).
The revision and addition read as
follows:
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Certificates of organic operation.
*
*
*
*
*
(b) The certifying agent must issue a
certificate of organic operation. The
certificate of organic operation must be
generated from the Organic Integrity
Database and may be provided to
certified operations electronically.
(c) In addition to the certificate of
organic operation provided for in
paragraph (b) of this section, a certifying
agent may issue its own addenda to the
certificate of organic operation. If
issued, any addenda must include:
(1) Name, address, and contact
information for the certified operation;
(2) The certified operation’s unique ID
number/code that corresponds to the
certified operation’s ID number/code in
the Organic Integrity Database;
(3) A link to the Organic Integrity
Database or a link to the certified
operation’s profile in the Organic
Integrity Database, along with a
statement, ‘‘You may verify the
certification of this operation at the
Organic Integrity Database,’’ or a similar
statement;
(4) Name, address, and contact
information of the certifying agent; and
(5) ‘‘Addendum issue date.’’
*
*
*
*
*
§ 205.405
[Amended]
17. Amend § 205.405 by removing
paragraph (c)(3).
■ 18. Amend 205.406 by revising
paragraphs (a) and (b) to read as follows:
■
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§ 205.406
Continuation of certification.
(a) To continue certification, a
certified operation must annually pay
the certification fees and submit the
following information to the certifying
agent:
(1) A summary statement, supported
by documentation, detailing any
deviations from, changes to,
modifications to, or other amendments
made to the organic system plan
submitted during the previous year;
(2) Any additions or deletions to the
previous year’s organic system plan,
intended to be undertaken in the
coming year, detailed pursuant to
§ 205.201;
(3) Any additions to or deletions from
the information required pursuant to
§ 205.401(b); and
(4) Other information as deemed
necessary by the certifying agent to
determine compliance with the Act and
the regulations in this part.
(b) The certifying agent must arrange
and conduct an on-site inspection,
pursuant to § 205.403, of the certified
operation at least once per calendar
year.
*
*
*
*
*
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§ 205.500
[Amended]
19. Amend § 205.500 by removing
paragraph (c).
■ 20. Section 205.501 is amended by:
■ a. Revising paragraphs (a)(4), (5), (6),
(10), (13), and (15);
■ b. Redesignating paragraph (a)(21) as
paragraph (a)(23); and
■ c. Adding new paragraph (a)(21) and
paragraph (a)(22).
The revisions and additions read as
follows:
■
§ 205.501 General requirements for
accreditation.
(a) * * *
(4) Continuously use a sufficient
number of qualified and adequately
trained personnel, including inspectors
and certification review personnel, to
comply with and implement the USDA
organic standards.
(i) Certifying agents must demonstrate
that all inspectors, including staff,
volunteers, and contractors, have the
relevant knowledge, skills, and
experience required to inspect
operations of the scope and complexity
assigned and to evaluate compliance
with the applicable regulations of this
part.
(A) Certifying agents must
demonstrate that inspectors
continuously maintain adequate
knowledge and skills about the current
USDA organic standards, production
and handling practices, certification and
inspection, import and/or export
requirements, traceability audits, massbalance audits, written and oral
communication skills, sample
collection, investigation techniques, and
preparation of technically accurate
inspection documents.
(B) All inspectors must demonstrate
successful completion of training that is
relevant to inspection. Inspectors with
less than one year of inspection
experience must complete at least 50
hours of training within their first year
and prior to performing inspections
independently. Inspectors with one or
more years of inspection experience
must annually complete at least 10
hours of training if inspecting one area
of operation (as defined at § 205.2) and
an additional 5 hours of training for
each additional area of operation
inspected.
(C) Certifying agents must
demonstrate that inspectors have a
minimum of 2,000 hours of experience
relevant to the scope and complexity of
operations they will inspect before
assigning initial inspection
responsibilities.
(ii) Certifying agents must
demonstrate that all certification review
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personnel, including staff, volunteers, or
contractors, have the knowledge, skills,
and experience required to perform
certification review of operations of the
scope and complexity assigned and to
evaluate compliance with the applicable
regulations of this part.
(A) Certifying agents must
demonstrate that all certification review
personnel continuously maintain
adequate knowledge and skills in the
current USDA organic standards,
certification and compliance processes,
traceability audits, mass-balance audits,
and practices applicable to the type,
volume, and range of review activities
assigned.
(B) All certification review personnel
must demonstrate successful
completion of training that is relevant to
certification review. Certification review
personnel with less than one year of
certification review experience must
complete at least 50 hours of training
within their first year performing
certification review. Certification review
personnel with one or more years of
certification review experience must
annually complete at least 10 hours of
training if conducting certification
review related to one area of operation
and an additional 5 hours of training for
each additional area of operation.
(iii) Certifying agents must maintain
current training requirements, training
procedures, and training records for all
inspectors and certification review
personnel.
(5) Demonstrate that all persons with
inspection or certification review
responsibilities have sufficient expertise
in organic production or handling
techniques to successfully perform the
duties assigned. Sufficient expertise
must include knowledge of certification
to USDA organic standards and
evidence of education, training, or
professional experience in the fields of
agriculture, science, or organic
production and handling that relates to
assigned duties.
(6) Conduct an annual performance
evaluation of all persons who conduct
inspections, certification review, or
implement measures to correct any
deficiencies in certification services.
(i) Witness inspections—certifying
agents must ensure that each inspector
is evaluated while performing an
inspection at least once every three
years, or more frequently if warranted.
Inspectors with less than three years of
inspection experience must undergo a
witness inspection annually. Witness
inspections must be performed by
certifying agent personnel who are
qualified to evaluate inspectors.
(ii) Certifying agents must maintain
documented policies, procedures, and
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records for annual performance
evaluations and witness inspections.
*
*
*
*
*
(10) Maintain strict confidentiality
with respect to its clients under the
applicable organic certification program
and not disclose to third parties (except
for the Secretary or the applicable State
organic program’s governing State
official or their authorized
representatives) any business-related
information concerning any client
obtained while implementing the
regulations in this part, except:
(i) For information that must be made
available to any member of the public,
as provided for in § 205.504(b)(5);
(ii) For enforcement purposes,
certifying agents must exchange any
compliance-related information that is
credibly needed to certify, decertify, or
investigate an operation, including for
the purpose of verifying supply chain
traceability and audit trail
documentation; and
(iii) If a certified operation’s
proprietary business information is
compliance-related and thus credibly
needed to certify, decertify, or
investigate that operation, certifying
agents may exchange that information
for the purposes of enforcing the Act,
but the information in question still
retains its proprietary character even
after it is exchanged and all of the
certifying agents that are involved in the
exchange still have a duty to preserve
the confidentiality of that information
after the exchange.
*
*
*
*
*
(13) Accept the certification decisions
made by another certifying agent
accredited or accepted by USDA
pursuant to § 205.500. Certifying agents
must provide information to other
certifying agents to ensure organic
integrity or to enforce organic
regulations, including to verify supply
chain integrity, authenticate the organic
status of certified products, and conduct
investigations;
*
*
*
*
*
(15) Maintain current and accurate
data in the Organic Integrity Database
for each operation which it certifies;
*
*
*
*
*
(21) Conduct risk-based supply chain
traceability audits as described in the
criteria and procedures for supply chain
audits, per § 205.504(b)(7), and share
audit findings with other certifying
agents as needed to determine
compliance, per paragraph (a)(13) of this
section.
(22) Notify AMS not later than 90
calendar days after certification
activities begin in a new certification
office. The notification must include the
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countries where the certification
activities are being provided, the nature
of the certification activities, and the
qualifications of the personnel
providing the certification activities.
*
*
*
*
*
■ 21. Section 205.504 is amended by
revising the introductory text and
paragraph (b)(4) and adding paragraphs
(b)(7) and (8) to read as follows:
§ 205.504
ability.
Evidence of expertise and
A private or governmental entity
seeking accreditation as a certifying
agent must submit the following
documents and information to
demonstrate its expertise in organic
production or handling techniques; its
ability to fully comply with and
implement the organic certification
program established in §§ 205.100 and
205.101, 205.201 through 205.203,
205.300 through 205.303, 205.400
through 205.406, and 205.661 through
205.663; and its ability to comply with
the requirements for accreditation set
forth in § 205.501:
*
*
*
*
*
(b) * * *
(4) A copy of the procedures to be
used for sharing information with other
certifying agents and for maintaining the
confidentiality of any business-related
information as set forth in
§ 205.501(a)(10);
*
*
*
*
*
(7) A copy of the criteria to identify
high-risk operations and agricultural
products for supply chain traceability
audits; and procedures to conduct riskbased supply chain traceability audits,
as required in § 205.501(a)(21); and
procedures to report credible evidence
of organic fraud to the Administrator.
(8) A copy of reasonable decision
criteria for acceptance of mediation, and
a process for identifying personnel
conducting mediation and setting up
mediation.
*
*
*
*
*
■ 22. Add § 205.511 to subpart F to read
as follows:
§ 205.511 Accepting foreign conformity
assessment systems.
(a) Foreign product may be certified
under the USDA organic regulations by
a USDA-accredited certifying agent and
imported for sale in the United States.
Foreign product that is produced and
handled under another country’s
organic certification program may be
sold, labeled, or represented in the
United States as organically produced if
the U.S. Government determines that
such country’s organic certification
program provides technical
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requirements and a conformity
assessment system governing the
production and handling of such
products that are at least equivalent to
the requirements of the Act and the
regulations in this part.
(b) Countries desiring to establish
eligibility of product certified under that
country’s organic certification program
to be sold, labeled, or represented in the
United States as organically produced
may request equivalence determinations
from AMS. A foreign government must
maintain compliance and enforcement
mechanisms to ensure that its organic
certification program is fully meeting
the terms and conditions of any
equivalence determination provided by
the U.S. Government pursuant to this
section. To request an equivalence
determination, the requesting country
must submit documentation that fully
describes its technical requirements and
conformity assessment system. If the
U.S. Government determines it can
proceed, AMS will assess the country’s
organic certification program to evaluate
if it is equivalent.
(c) USDA, working with other Federal
agencies, will describe the scope of an
equivalence determination.
(d) AMS will conduct regular reviews
and reassessments of countries deemed
equivalent to verify that the foreign
government’s technical requirements
and conformity assessment system
continue to be at least equivalent to the
requirements of the Act and the
regulations of this part, and will
determine if the equivalence
determination should be continued,
amended, or terminated. AMS will
determine the timing and scope of
reviews and re-assessments based on,
but not limited to, factors such as: the
terms of the equivalence determination,
changes to the foreign country’s
technical requirements or conformity
assessment system, the results of
previous reviews and re-assessments,
instances of suspected or verified
noncompliance issues, the volume of
trade, and other factors contributing to
the risk level of the equivalence
determination.
(e) The U.S. Government may
terminate an equivalence determination
if the terms or conditions established
under the equivalence determination are
not met; if AMS determines that the
country’s technical requirements and/or
conformity assessment program are no
longer equivalent; if AMS determines
that the foreign government’s organic
control system is inadequate to ensure
that the country’s organic certification
program is fully meeting the terms and
conditions under the equivalence
determination; or for other good cause.
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Federal Register / Vol. 88, No. 12 / Thursday, January 19, 2023 / Rules and Regulations
23. Amend § 205.660 by redesignating
paragraphs (c) and (d) as paragraphs (d)
and (e) and adding new paragraph (c).
The addition reads as follows:
■
§ 205.660
General.
*
*
*
*
*
(c) The Program Manager may initiate
enforcement action against any person
who sells, labels, or provides other
market information concerning an
agricultural product if such label or
information implies that such product is
produced or handled using organic
methods, if the product was produced
or handled in violation of the Organic
Foods Production Act or the regulations
in this part.
*
*
*
*
*
■ 24. Amend § 205.661 by revising the
section heading to read as follows:
§ 205.661
Investigation.
*
*
*
*
*
■ 25. Section 205.662 is amended by:
■ a. Adding paragraph (e)(3);
■ b. Revising the first sentence of
paragraph (f)(1); and
■ c. Revising paragraph (g)(1).
The addition and revisions read as
follows:
§ 205.662 Noncompliance procedure for
certified operations.
khammond on DSKJM1Z7X2PROD with RULES2
*
*
*
*
*
(e) * * *
(3) Within 3 business days of issuing
a notification of suspension or
revocation, or the effective date of an
operation’s surrender, the certifying
agent must update the operation’s status
in the Organic Integrity Database.
(f) * * *
(1) A certified operation or a person
responsibly connected with an
operation whose certification has been
suspended may at any time, unless
otherwise stated in the notification of
suspension, submit a request to the
Secretary for reinstatement of its
certification, or submit a request for
eligibility to be certified. * * *
*
*
*
*
*
(g) * * *
(1) Knowingly sells or labels a
product as organic, except in
accordance with the Act, shall be
subject to a civil penalty of not more
than the amount specified in 7 CFR
3.91(b)(1)(xxxvi) per violation.
*
*
*
*
*
■ 26. Revise § 205.663 to read as
follows:
§ 205.663
Mediation.
(a) A certifying agent must submit
with its administrative policies and
procedures: decision criteria for
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acceptance of mediation, and a process
for identifying personnel conducting
mediation and setting up mediation
sessions per § 205.504(b)(8).
(b) A certified operation or applicant
for certification may request mediation
to resolve a denial of certification or
proposed suspension or proposed
revocation of certification issued by a
certifying agent or State organic
program.
(1) A certified operation or applicant
for certification must submit any request
for mediation in writing to the
applicable certifying agent or State
organic program within 30 calendar
days of receipt of the notice of proposed
suspension or proposed revocation of
certification or denial of certification.
(2) A certifying agent or State organic
program may accept or reject a request
for mediation based on the decision
criteria required in paragraph (a) of this
section. Certifying agents must
document these criteria and how the
certifying agent applied the criteria to
the request.
(3) If a certifying agent rejects a
mediation request, it must provide this
rejection, and the justification for the
rejection, in writing to the applicant for
certification or certified operation. The
rejection must include the right to
request an appeal, pursuant to
§ 205.681, within 30 calendar days of
the date of receipt of the written
notification of rejection of the request
for mediation.
(4) When an operation appeals a
rejection of mediation, the adverse
action which is contested must not be
finalized during the appeal proceeding.
(c) Both parties must agree on the
person conducting the mediation.
(d) If a State organic program is in
effect, the parties must follow the
mediation procedures established in the
State organic program and approved by
the Secretary.
(e) The parties to the mediation have
a maximum of 30 calendar days from
the start of mediation to reach an
agreement. Successful mediation results
in a settlement agreement agreed to in
writing by both the certifying agent and
the certified operation. If mediation is
unsuccessful, the applicant for
certification or certified operation has
30 calendar days from receipt of a
written notice of termination of
mediation to appeal the denial of
certification or proposed suspension or
revocation pursuant to § 205.681.
(f) Any settlement agreement reached
through mediation must comply with
the Act and the regulations in this part.
The Program Manager may review any
mediated settlement agreement for
conformity to the Act and the
PO 00000
Frm 00080
Fmt 4701
Sfmt 4700
regulations in this part and may reject
any agreement or provision not in
conformance with the Act or the
regulations in this part.
(g) The Program Manager may
propose mediation and enter into a
settlement agreement at any time to
resolve any adverse action notice.
■ 27. Amend § 205.665 by revising
paragraph (a) to read as follows:
§ 205.665 Noncompliance procedure for
certifying agents.
(a) Notification. (1) A written
notification of noncompliance will be
sent to the certifying agent when:
(i) An inspection, review, or
investigation of an accredited certifying
agent by the Program Manager reveals
any noncompliance with the Act or
regulations in this part; or
(ii) The Program Manager determines
that the certification activities of the
certifying agent, or any person
performing certification activities on
behalf of the certifying agent, are not
compliant with the Act or the
regulations in this part; or
(iii) The Program Manager determines
that the certification activities at a
certification office, and/in specific
countries, are not compliant with the
Act or the regulations in this part.
(2) Such notification must provide:
(i) A description of each
noncompliance;
(ii) The facts upon which the
notification of noncompliance is based;
and
(iii) The date by which the certifying
agent must rebut or correct each
noncompliance and submit supporting
documentation of each correction when
correction is possible.
*
*
*
*
*
■ 28. Revise § 205.680 to read as
follows:
§ 205.680
General.
(a) Persons subject to the Act who
believe they are adversely affected by an
adverse action of the National Organic
Program’s Program Manager may appeal
such decision to the Administrator.
(b) Persons subject to the Act who
believe they are adversely affected by an
adverse action of a State organic
program may appeal such decision to
the State organic program’s governing
State official, who will initiate handling
of the appeal pursuant to appeal
procedures approved by the Secretary.
(c) Persons subject to the Act who
believe they are adversely affected by an
adverse action of a certifying agent may
appeal such decision to the
Administrator, Except, that, when the
person is subject to an approved State
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Federal Register / Vol. 88, No. 12 / Thursday, January 19, 2023 / Rules and Regulations
organic program, the appeal must be
made to the State organic program.
(d) Persons subject to the Act who
believe they are adversely affected by an
adverse action of a certifying agent or a
State organic program may request
mediation as provided in § 205.663.
(e) All appeals must comply with the
procedural requirements in § 205.681(c)
and (d).
(f) All written communications
between parties involved in appeal
proceedings must be sent to the
recipient’s place of business by a
delivery service which provides dated
return receipts.
(g) All appeals must be reviewed,
heard, and decided by persons not
involved with the adverse action being
appealed.
■ 29. Amend § 205.681 by revising
paragraph (a) introductory text and
paragraphs (a)(2), (b), (c), and (d)(1) and
(3) to read as follows:
§ 205.681
Appeals.
khammond on DSKJM1Z7X2PROD with RULES2
(a) Adverse actions by certifying
agents. An applicant for certification
may appeal a certifying agent’s notice of
denial of certification, and a certified
operation may appeal a certifying
agent’s notification of proposed
suspension or proposed revocation of
certification to the Administrator,
Except, that, when the applicant or
certified operation is subject to an
approved State organic program, the
appeal must be made to the State
organic program which will carry out
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18:59 Jan 18, 2023
Jkt 259001
the appeal pursuant to the State organic
program’s appeal procedures approved
by the Secretary.
*
*
*
*
*
(2) If the Administrator or State
organic program denies an appeal, a
formal administrative proceeding will
be initiated to deny, suspend, or revoke
the certification unless the parties
resolve the issues through settlement, or
the appellant waives or does not timely
request a hearing. Such proceeding must
be conducted pursuant to the U.S.
Department of Agriculture’s Uniform
Rules of Practice, 7 CFR part 1, subpart
H, or the State organic program’s rules
of procedure.
(b) Adverse actions by the NOP
Program Manager. A person affected by
an adverse action, as defined by § 205.2,
issued by the NOP Program Manager,
may appeal to the Administrator.
(1) If the Administrator sustains an
appeal, an applicant will be issued
accreditation, a certifying agent will
continue its accreditation, or an
operation will continue its certification,
a civil penalty will be withdrawn, and
a cease and desist notice will be
withdrawn, as applicable to the
operation.
(2) If the Administrator denies an
appeal, a formal administrative
proceeding will be initiated to deny,
suspend, or revoke the accreditation or
certification and/or levy civil penalties
unless the parties resolve the issues
through settlement, the appellant
PO 00000
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Fmt 4701
Sfmt 9990
3627
waives a hearing, or the appellant does
not timely request a hearing. Such
proceeding must be conducted pursuant
to the U.S. Department of Agriculture’s
Uniform Rules of Practice, 7 CFR part 1,
subpart H.
(c) Filing period. An appeal must be
filed in writing within the time period
provided in the letter of notification or
within 30 days from receipt of the
notification, whichever occurs later. The
appeal will be considered ‘‘filed’’ on the
date received by the Administrator or by
the State organic program. An adverse
action will become final and
nonappealable unless an appeal is
timely filed.
(d) * * *
(1) Appeals to the Administrator and
Requests for Hearing must be filed in
writing and addressed to: 1400
Independence Ave. SW, Room 2642,
Stop 0268, Washington, DC 20250, or
electronic transmission, NOPAppeals@
usda.gov.
*
*
*
*
*
(3) All appeals must include a copy of
the adverse action and a statement of
the appellant’s reasons for believing that
the action was not proper or made in
accordance with applicable program
regulations.
Erin Morris,
Associate Administrator, Agricultural
Marketing Service.
[FR Doc. 2023–00702 Filed 1–18–23; 8:45 am]
BILLING CODE 3410–02–P
E:\FR\FM\19JAR2.SGM
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Agencies
[Federal Register Volume 88, Number 12 (Thursday, January 19, 2023)]
[Rules and Regulations]
[Pages 3548-3627]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-00702]
[[Page 3547]]
Vol. 88
Thursday,
No. 12
January 19, 2023
Part III
Department of Agriculture
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7 CFR Part 205
National Organic Program (NOP); Strengthening Organic Enforcement;
Final Rule
Federal Register / Vol. 88 , No. 12 / Thursday, January 19, 2023 /
Rules and Regulations
[[Page 3548]]
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DEPARTMENT OF AGRICULTURE
Agricultural Marketing Service
7 CFR Part 205
[Doc. No. AMS-NOP-17-0065; NOP-17-02]
RIN 0581-AD09
National Organic Program (NOP); Strengthening Organic Enforcement
AGENCY: Agricultural Marketing Service, USDA.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This rulemaking amends the United States Department of
Agriculture (USDA) organic regulations to strengthen oversight and
enforcement of the production, handling, and sale of organic
agricultural products. The amendments protect integrity in the organic
supply chain and build consumer and industry trust in the USDA organic
label by strengthening organic control systems, improving farm to
market traceability, and providing robust enforcement of the USDA
organic regulations. Topics addressed in this rulemaking include:
applicability of the regulations and exemptions from organic
certification; National Organic Program Import Certificates;
recordkeeping and product traceability; certifying agent personnel
qualifications and training; standardized certificates of organic
operation; unannounced on-site inspections of certified operations;
oversight of certification activities; foreign conformity assessment
systems; certification of producer group operations; labeling of
nonretail containers; annual update requirements for certified
operations; compliance and appeals processes; and calculating organic
content of multi-ingredient products.
DATES:
Effective date: March 20, 2023
Implementation date: March 19, 2024.
FOR FURTHER INFORMATION CONTACT: Jennifer Tucker, Ph.D., Deputy
Administrator, National Organic Program. Telephone: 202-720-3252.
Email: [email protected].
SUPPLEMENTARY INFORMATION:
I. Executive Summary
This rulemaking amends several sections of the USDA organic
regulations, 7CFR part 205, to strengthen oversight of the production,
handling, certification, marketing, and sale of organic agricultural
products as established by the Organic Foods Production Act of 1990
(OFPA, or ``the Act'').\1\ When implemented, this rulemaking will
improve organic integrity across the organic supply chain, and benefit
stakeholders throughout the organic industry. These amendments close
gaps in the current regulations to build consistent certification
practices to deter and detect organic fraud, and improve transparency
and product traceability. In addition, the amendments will assure
consumers that organic products meet a robust, consistent standard and
reinforce the value of the organic label.
---------------------------------------------------------------------------
\1\ The Organic Foods Production Act of 1990, 7 U.S.C. 6501-
6524, is the statute from which the Agricultural Marketing Service
derives authority to administer the NOP and authority to amend the
regulations as describedin thisrulemaking. This document is
available at: https://uscode.house.gov/view.xhtml?path=/[email protected]/chapter94&edition=prelim
---------------------------------------------------------------------------
The need for this rulemaking is driven by organic market growth and
increasingly complex organic supply chains. Today's organic market is
characterized by long--and often global--supply chains where organic
products are handled by many businesses before reaching the consumer.
Often, these businesses are not certified organic--and therefore have
no oversight from the USDA or USDA-accredited certifying agents. The
absence of direct enforcement over some entities in the organic supply
chain, in combination with price premiums for organic products, has
created the opportunity for organic fraud. The amendments in this
rulemaking are designed to mitigate the occurrence of organic fraud.
The Agricultural Marketing Service (AMS) is confident in the
integrity and value of the USDA organic seal. Consumers can trust the
organic label due to a rigorous oversight system that operates
globally. However, the challenges of modern organic supply chains
demand action to strengthen enforcement and uphold the integrity of the
USDA organic label.
This rulemaking strengthens enforcement of the USDA organic
regulations through several actions mandated by the Agriculture
Improvement Act of 2018:
1. Reduce the types of uncertified entities in the organic supply
chain that operate without USDA oversight--including importers, certain
brokers, and traders of organic products. This will safeguard organic
product integrity and improve traceability.
2. Require the use of NOP Import Certificates for all organic
products entering the United States. This change expands the use of NOP
Import Certificates to all organic products imported into the United
States, improving the oversight and traceability of imported organic
products.
3. Clarify the NOP's authority to oversee certification activities,
including the authority to act against an agent or office of a
certifying agent. Additionally, certifying agents must notify the NOP
upon opening a new office, which will allow the NOP to provide more
effective and consistent oversight of certifying agents and their
activities.
Additionally, this rule includes several essential actions that
work in alignment with the provisions above to further strengthen
enforcement of the USDA organic regulations:
1. Require that nonretail containers used to ship or store organic
products are labeled with organic identity and are traceable to audit
trail documentation. This information will clearly identify organic
products, reduce the mishandling of organic products, and support
traceability.
2. Require certifying agents to conduct unannounced inspections of
at least 5% of the operations they certify, complete mass-balance
audits during annual on-site inspections, and verify traceability back
to the previous certified operation in the supply chain during annual
on-site inspections.
3. Require certifying agents to issue standardized certificates of
organic operation generated from the USDA's Organic Integrity Database
(OID); this will simplify the verification of valid certificates of
organic operation. Certifying agents must also keep accurate and
current certified operation data in OID, which will further support
verification of operations' certified status.
4. Clarify how certified operations may submit changes to their
organic system plan, with the goal of reducing paperwork burden for
organic operations and certifying agents. This rule also builds
consistency in certification practices by clarifying that certifying
agents must conduct on-site inspections at least once per calendar
year.
5. Establish specific qualification and training requirements for
certifying agent personnel, including inspectors and certification
reviewers. Requiring that personnel meet minimum education and
experience qualifications and requiring continuing education will
ensure high-quality and consistent certification activities across all
certifying agents.
6. Clarify conditions for establishing, evaluating, and terminating
equivalence determinations with foreign government organic programs,
based on an
[[Page 3549]]
evaluation of their organic foreign conformity systems. This will
ensure the compliance of organic products imported from countries that
have organic trade arrangements or agreements with the United States.
7. Clarify that the NOP may initiate enforcement action against any
violator of the OFPA, including uncertified operations and responsibly
connected parties; clarify what actions may be appealed and by whom;
and clarify NOP's appeal procedures and options for mediation
(alternative dispute resolution).
8. Specify certification requirements for producer group
operations, to provide consistent, enforceable standards and ensure
compliance with the USDA organic regulations. Producer groups must meet
certain criteria to qualify for certification, and must use an internal
control system to monitor compliance.
9. Clarify the method of calculating the percentage of organic
ingredients in a multi-ingredient product to promote consistent
interpretation and application of the regulation.
10. Require certified operations to develop and implement improved
recordkeeping and organic fraud prevention processes and procedures;
require certifying agents to conduct supply chain traceability audits
and to develop and implement information-sharing processes.
Costs and Benefits
AMS estimates the following costs and benefits of this rule:
Costs and Benefits of SOE Rulemaking
----------------------------------------------------------------------------------------------------------------
Average annual cost \a\ Total cost \b\
---------------------------------------------------------------
3% Discount 7% Discount 3% Discount 7% Discount
rate rate rate rate
----------------------------------------------------------------------------------------------------------------
Domestic Costs.................................. $10,548,510 $7,884,601 $158,227,651 $118,269,011
Foreign Costs................................... 8,769,681 6,550,892 131,545,210 98,263,398
---------------------------------------------------------------
Total Costs................................. 19,318,191 14,435,494 289,772,861 216,532,409
---------------------------------------------------------------
Benefits.................................... 32,944,812 24,272,099 494,172,179 364,081,491
----------------------------------------------------------------------------------------------------------------
\a\ Estimated annual averages of the 15-year Net Present Value domestic costs discounted at 3 and 7 percent.
\b\ Estimated total domestic costs for affected industry in Net Present Value discounted at 3 and 7 percent.
Table of Contents
I. Executive Summary
II. Background
A. Authority
B. Purpose and Need for the Rule
C. History
D. Public Comment
E. Terminology
F. Does this action apply to me?
G. Compliance Date
III. Overview of Amendments
A. Applicability and Exemptions From Certification
B. Imports to the United States
C. Labeling of Nonretail Containers
D. On-Site Inspections
E. Certificates of Organic Operation
F. Continuation of Certification
G. Paperwork Submissions to the Administrator
H. Personnel Training and Qualifications
I. Oversight of Certification Activities
J. Accepting Foreign Conformity Assessment Systems
K. Compliance and Noncompliance Procedures
L. Mediation
M. Adverse Action Appeal Process
N. Producer Group Operations
O. Calculating the Percentage of Organically Produced
Ingredients
P. Supply Chain Traceability and Organic Fraud Prevention
Q. Technical Corrections
R. Additional Amendments Considered but Not Included in This
Rule
IV. Regulatory Analyses
A. Summary of Economic Analyses
B. Regulatory Impact Analysis
C. Executive Order 12988
D. Paperwork Reduction Act
E. Executive Order 13175
F. Executive Order 13132
G. Civil Rights Impact Analysis
H. Related Documents
II. Background
A. Authority
The Organic Foods Production Act of 1990 (OFPA) (7 U.S.C. 6501-
6524), authorizes the Agricultural Marketing Service (AMS) to establish
and maintain national standards governing the marketing of organically
produced agricultural products. AMS administers these standards through
the National Organic Program (NOP). Final regulations implementing the
NOP, also referred to as the USDA organic regulations, were published
on December 21, 2000 (65 FR 80548) and became effective on October 21,
2002.\2\ Through these regulations, AMS oversees national standards for
the production, handling, labeling, and sale of organically produced
agricultural products.
---------------------------------------------------------------------------
\2\ 7 CFR part 205 National Organic Program; Final Rule.
December 21, 2000. Available on the AMS website: https://www.federalregister.gov/documents/2000/12/21/00-32257/national-organic-program
---------------------------------------------------------------------------
B. Purpose and Need for the Rule
Since full implementation of the USDA organic regulations, the
organic industry has experienced significant change. Both demand for
and sales of organic products have risen steadily; total U.S. sales of
organic products reached more than $63 billion in 2021.\3\ The number
of businesses producing, handling, marketing, and selling organic
products has also grown to meet consumer demand. Rapid growth has
attracted many businesses to the USDA organic label and increased the
complexity of global organic supply chains.
---------------------------------------------------------------------------
\3\ Organic Trade Association, Organic Industry Survey, 2022.
---------------------------------------------------------------------------
Complexity makes oversight and enforcement of the organic supply
chains difficult because organic products are credence goods, which
means that their organic attributes, or ``integrity,'' cannot be easily
verified by consumers or businesses who buy organic products for use or
resale. The elements needed to guarantee organic integrity--transparent
supply chains, trusted interactions between businesses, and mechanisms
to verify product legitimacy--are more difficult to achieve in the
increasingly complex modern organic industry. This is further
compounded by inconsistent interpretation and implementation of the
USDA organic regulations, caused by a lack of clarity in some portions
of the regulation.
AMS is confident in the integrity and value of the USDA organic
seal. Consumers can trust the organic label due to a rigorous oversight
system that operates globally. However, the above challenges sometimes
cause
[[Page 3550]]
mishandling of organic products, where integrity is compromised due to
improper handling. Additionally, high demand for organic products, the
absence of direct enforcement over some entities in the organic supply
chain, and organic price premiums increase the opportunity and
incentive for organic fraud (when nonorganic products are deceptively
represented as organic).
This rule addresses these risks and challenges by expanding
oversight to higher-risk portions of organic supply chains, requiring
organic operations to implement traceability and verification best
practices, and clarifying oversight and enforcement practices to ensure
more consistent implementation by certifying agents. This rule will
help prevent loss of organic integrity--which can occur both through
unintentional mishandling of organic products, and intentional fraud
meant to deceive--and strengthen the trust consumers, farmers, and
businesses have in the USDA organic label.
Mishandling of Organic Products and Complex Supply Chains
One of the most common risks to the integrity of an organic product
is mishandling--when an entity unintentionally compromises the unique
attributes that make a product organic. Once organic integrity is
compromised, that product can no longer be sold as organic, and both
its unique attributes and price premium are forfeit. Mishandling can
occur at any point in a supply chain, including production, handling,
transport, storage, sale, and processing. Examples of mishandling that
can cause a loss of integrity include exposure to pesticides,
fertilizers, fumigants, or cleaning agents that are not permitted in
organic production; mixing (``commingling'') of organic and nonorganic
products; relabeling or repackaging with incorrect identification; and
inability to demonstrate organic status due to poor or incomplete
information in records or transaction paperwork. The likelihood of such
mishandling is greater in long, complex supply chains where many
businesses, including businesses not certified organic, handle and sell
organic products.
When the organic regulations were published in 2000, organic
products were marketed mostly locally or regionally, and supply chains
tended to be short and transparent; for example, farm to wholesale to
retail to consumer. Demand and sales have grown considerably since
then. This significant market growth has attracted more producers,
handlers, product suppliers, importers, brokers, distributors, and
others to the organic market. Consider the example of an organic egg
supply chain in the United States, beginning with the production of
certified organic corn and ending with the sale of eggs to the
consumer. This demonstrates the typical entities and transactions in an
organic supply chain under the existing regulations:
A certified organic farm produces organic corn.
The corn is transported via an uncertified truck to a
local grain elevator, where it is aggregated with other organic corn
from nearby producers.
An uncertified commodity trader buys the corn.
The corn is transported via uncertified truck to an
uncertified storage facility; both transport and storage are
subcontracted and are not owned by the commodity trader.
The commodity trader sells the corn to a certified organic
grain supplier; the two parties remain anonymous because they use an
uncertified broker to facilitate the transaction.
The corn is transported via uncertified rail and river
barge to the grain supplier; it is transloaded and stored temporarily
several times before being delivered to the certified grain supplier.
The certified organic grain supplier stores the corn and
combines it with imported organic corn purchased from an importer via
an uncertified broker.
The certified grain supplier sells the corn to a certified
organic feed processer; the corn is transported via an uncertified
truck.
The certified processer combines the corn with several
other ingredients to create organic chicken feed.
The certified processer sells the feed to a certified
organic egg producer and transports it via an uncertified truck.
The certified organic egg producer sells organic eggs to
an uncertified distributor.
The uncertified distributor sells the organic eggs to a
retailer prior to final sale to the consumer.
This example illustrates the supply chain for a single ingredient--
organic feed corn. The supply chain for the organic eggs at the end of
this example is even more complex because it includes other ingredients
that go into the chicken feed (e.g., soybean meal, oats, wheat, seed
oils). Many of these ingredients are sourced both domestically and
internationally. Each ingredient has its own unique supply chain;
together they create a complex web converging on a single organic
product. It is largely because of this complexity that this rule
introduces more specific traceability, verification, oversight, and
enforcement practices for high-risk portions of organic supply chains.
Organic Fraud
In addition to mishandling, a growing risk to organic integrity is
fraud--the deceptive representation, sale, or labeling of nonorganic
agricultural products as organic. High demand for organic products, the
absence of direct enforcement over some entities in the organic supply
chain, and organic price premiums have increased the opportunity and
incentive for organic fraud. Both NOP and organic stakeholders have
uncovered organic fraud in organic supply chains, particularly in
organic grain and oilseed supply chains. Because such supply chains are
complex and involve multiple changes in ownership of high demand
products, the incentive for fraud is high. Federal investigations show
that organic grain and oilseed fraud can lead to tens of millions of
dollars in fraudulent sales within just a few months. The following
examples highlight some of the types of organic fraud that this rule
seeks to prevent. The examples also demonstrate the magnitude of total
organic fraud and how this rule's additional oversight and enforcement
mechanisms will reduce fraud.
In 2019, four individuals were sentenced to prison terms
for their roles in an organic grain fraud ring. The charges were
brought by the U.S. Attorney's Office for the Northern District of
Iowa. All four were sentenced to prison terms. The lead defendant, who
was sentenced to more than ten years, pled guilty to defrauding
customers in a scheme involving at least $142 million in nonorganic
grains sold as organic. The lead defendant sold fraudulent grain to
customers over a period of seven years, claiming the product was
organically grown in Nebraska and Missouri.\4\ This rule includes more
robust traceability and verification practices that would have helped
identify and stop this type of fraud earlier, preventing further sale
of the fraudulent products and reducing the impact of the fraud.
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\4\ https://www.justice.gov/usao-ndia/pr/field-schemes-fraud-results-over-decade-federal-prison-leader-largest-organic-fraud.
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In February 2020, a federal grand jury indicted an
individual in South Dakota for allegedly selling $71 million of
nonorganic grains and oilseeds falsely labeled organic between 2012 and
[[Page 3551]]
2018.\5\ The defendant pled guilty and was sentenced in 2021 to 51
months in federal prison. He was also ordered to pay more than $15
million in restitution. The fraud ring spanned multiple states. After
NOP revoked the business' organic certifications, the responsible
parties established new brokerage firms to continue their fraud. Under
the current organic regulations, these brokerages did not require
organic certification and NOP had no oversight of their activities.
This rule will require the certification and oversight of brokers like
those involved in this case. This would allow the NOP to identify and
prevent the fraud, minimizing damage to the U.S. market.
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\5\ https://www.wisfarmer.com/story/news/2020/02/18/south-dakota-man-indicted-71-million-organics-fraud/4801207002/. https://www.justice.gov/usao-sd/pr/florida-man-sentenced-conspiracy-commit-wire-fraud-and-money-laundering.
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In 2017, an investigation revealed three shipments of
imported ``organic'' corn and soybeans--each weighing between 36 and 46
million pounds--were fraudulently labeled as organic. The associated
transaction records indicated that all three shipments originated from
producers in the Black Sea region that were not certified organic, and
that the shipments were originally sold at lower conventional prices.
In one case, a shipment of soybeans had been fumigated with aluminum
phosphide, which is prohibited for use in organic production and
handling. By the time this fraud was discovered, about 21 million
pounds of this same shipment of soybeans had already been distributed--
primary to organic producers as livestock feed.\6\ This rule will
require the use of NOP Import Certificates to verify the source and
integrity of organic imports, which will help detect and prevent
fraudulently labeled imports, such as those in this example, from
entering domestic supply chains.
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\6\ https://www.washingtonpost.com/business/economy/the-labels-said-organic-but-these-massive-imports-of-corn-and-soybeans-werent/2017/05/12/6d165984-2b76-11e7-a616-d7c8a68c1a66_story.html.
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In July 2022, a Minnesota farmer was indicted for growing
and selling fraudulent organic grains worth more than $46 million. The
farmer was certified organic but was growing grains with synthetic
fertilizers and pesticides in violation of the USDA organic
regulations. He sold this conventional grain (both what he produced
conventionally as well as conventional grain he purchased) as organic,
fraudulently presenting his certificate of organic operation to claim
the grain was organic and withholding the grain's true status from
buyers.\7\ This rule includes more robust traceability and verification
practices that would have helped identify and stop this type of fraud
earlier, preventing further sale of the fraudulent products and
reducing the impact of the fraud.
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\7\ https://www.justice.gov/usao-mn/pr/cottonwood-county-farmer-charged-46-million-organic-grain-fraud-scheme.
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In several of the above examples, fraudulent livestock feed was
sold to certified organic livestock producers, magnifying the effects
of the fraud. NOP continues to investigate complaints and multiple
cases of organic fraud at the production and handling levels. These
examples demonstrate the magnitude of fraud that NOP intercepts with
current oversight and enforcement techniques. SOE will significantly
bolster the oversight and enforcement mechanisms that NOP, certifying
agents, and operations have at their disposal. In the fraud cases
discussed above, these mechanisms would have allowed earlier fraud
detection and more effective enforcement action and would have greatly
reduced or even prevented the fraud.
Patterns in USDA Organic Certification and Organic Imports
The scope and distribution of potential organic fraud can also be
seen in changes in the number of operations certified to the USDA
organic standards and changes in the amount of organic imports from
certain regions. Two recent NOP efforts show both the potential type
and magnitude of fraud in the marketplace; more importantly, they also
demonstrate the potential of improved oversight and enforcement
mechanisms.
In 2018 and 2019, NOP began making changes to improve oversight of
organic imports, especially grain and oilseed imports from the Black
Sea region. NOP conducted farm-level yield analysis to compare expected
and actual yield, supply chain research to better understand the roles
and relationships of high-risk entities, and targeted import
surveillance to investigate credible reports of suspected fraud. As a
result of this heightened oversight and enforcement action, at least
180 operations (60 percent) in the Black Sea region have lost their
organic certification. In 2016, imports from the Black Sea region
represented 49 percent of the total dollar value of imported organic
grain and oilseeds (including corn, soybeans, wheat, barley,
sunflowers, flaxseed, and peas). In 2018, imports of these grains and
oilseeds from the region had dropped to 21 percent of the total dollar
value. The steep drop in organic certification and downward supply
trend in the Black Sea region give an indication of the magnitude and
type of fraud, as well as the success of stronger oversight and
enforcement strategy. Despite this enforcement success, key gaps in
oversight remain, such as uncertified entities in import supply chains
and non-mandatory use of NOP Import Certificates. This rule will help
close these gaps and bolster NOP's ability to detect and prevent
fraudulent organic imports.
In January 2021, AMS announced it would end its U.S.-India organic
recognition, which had allowed India's Agricultural and Processed Food
Products Export Development Authority (APEDA) to accredit certifying
agents to provide USDA organic certification in India. AMS ended this
recognition because NOP audits consistently found India's organic
control system to be insufficient to protect the integrity of the USDA
organic seal. In late 2020, prior to the end of U.S.-India recognition,
there were 4,023 operations certified to the USDA organic standard in
India. Operations formerly certified by AEDPA-accredited certifying
agents were given an 18-month transition period to become certified by
a USDA-accredited certifying agent. Since the end of the transition
period in July 2022, only 1,471 operations in India remain certified to
the USDA organic standard. Because failure to become recertified may
indicate an inability to comply with the USDA organic regulations, this
significant (63 percent) drop in the number of certified operations may
indicate the general volume of noncompliant activity (including
mishandling and fraud) that may have been taking place under the former
recognition. Additionally, following the end of the U.S. -India
recognition, imports of certified organic products from India has
dropped from an average per quarter value of $15.6 million to $9.4
million, a 39 percent decrease. This drop in import value suggests that
a significant number of organic imports from India may not have been
fully compliant with the USDA organic standard. The end of the U.S.-
India recognition demonstrates both the magnitude of potential fraud in
the market, and how more effective oversight (in this case,
certification only by USDA-accredited certifying agents) can
successfully safeguard the integrity of the USDA organic label. Despite
this success, there are still gaps in the oversight of foreign-
accredited certifying agents and imports from these countries.
[[Page 3552]]
This rule will allow NOP to more fully implement its oversight
authority by codifying specific procedures for evaluating, accepting,
and continuing equivalency or recognition with foreign organic
programs.
These examples demonstrate how applying oversight and enforcement
best practices can reduce organic fraud. SOE will reduce fraud by
codifying best practices in critical areas--exemptions from
certification, import oversight, traceability, recordkeeping,
inspections and audits, oversight of certifying agents, and assessment
of organic trade partners. Additionally, the examples above only show
the positive results of improved oversight and enforcement at the
federal level; SOE will build upon this success by requiring certifying
agents and organic operations to use similar techniques. This means
proven oversight and enforcement techniques will be deployed closer to
where fraud occurs, which will facilitate earlier detection, stop more
fraud before it cascades further into supply chains, and more directly
deter fraudulent actors. Because this rule codifies best practices and
requires key parties in organic supply chains use these practices, AMS
expects that SOE's benefits will exceed those demonstrated in the
examples above.
C. History
In response to their experiences in the organic system,
stakeholders have called for the NOP to take steps to improve oversight
of organic systems and enforcement of the USDA organic regulations.
Commonly cited areas for improvement include certification of excluded
handlers, organic import oversight, fraud prevention, organic trade
arrangements, and organic inspector qualifications. Public discussions
on many topics included in this rule occurred during multiple National
Organic Standards Board (NOSB) meetings.\8\
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\8\ The April 2021 NOSB meeting is the most recent example of a
public discussion to address fraud concerns in the organic supply
chain. A discussion document, meeting transcripts, and public
comments are available at https://www.ams.usda.gov/event/national-organic-standards-board-nosb-meeting-crystal-city-va-0.
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This rule seeks to strengthen enforcement of the USDA organic
regulations and protect the integrity of the organic label by (1)
strengthening organic control systems; (2) improving organic import
oversight; (3) clarifying organic certification standards; and (4)
enhancing supply chain traceability. AMS identified the need for these
changes through:
Direct experience in administering the NOP, particularly
complaint investigations and audits of accredited certifying agents;
The Agriculture Improvement Act of 2018,\9\ which amended
the OFPA.
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\9\ The Agriculture Improvement Act of 2018, Public Law No: 115-
334, is available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
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Recommendations of a 2017 Office of Inspector General
report; \10\
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\10\ USDA Office of Inspector General Audit Report 01601-0001-
21: National Organic Program International Trade Arrangements and
Agreements. September 2017: https://www.usda.gov/sites/default/files/01601-0001-21.pdf.
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Recommendations of the NOP's federal advisory committee,
the National Organic Standards Board (NOSB); and
Industry stakeholder and consumer feedback.
AMS expects the amendments will bring more effective oversight and
enforcement, improve organic integrity and product traceability,
clarify existing standards to ensure fair competition, bolster consumer
trust in the organic label, reduce organic fraud, and support continued
industry growth. Information about each amendment is described in more
detail below.
D. Public Comment
AMS published the Strengthening Organic Enforcement proposed rule
on August 5, 2020, opening a 60-day public comment period. AMS received
more than 1,500 public comments from a variety of stakeholders,
including certifying agents, certified organic producers and handlers,
uncertified handlers, retailers, organic inspectors, trade
associations, organic advocates, scientific organizations, government
organizations, and consumers. The majority of public comments supported
the proposed amendments and agreed that the rule is needed to improve
oversight and enforcement, drive consistent implementation of the
organic regulations, and reduce organic fraud.
Many stakeholders provided meaningful feedback about the proposed
policy revisions, including recommendations to improve the rule through
greater specificity and clarity. Others discussed how the proposed
amendments would affect them or suggested alternatives to the proposed
policies. Popular topics of discussion included the need for
certification; excluded handlers; exemptions from certification;
implementation of the mandatory NOP Import Certificate requirements;
supply chain traceability audits; recordkeeping and verification
requirements; fraud prevention plans for certified operations;
oversight of producer groups; qualifications and training requirements
for certifying agent personnel; labeling of nonretail containers; and
unannounced inspections.
Some comments also discussed the proposed implementation timeframe
of one year after publication of the final rule. Some comments asked
AMS to implement the rule immediately, while others agreed that a one-
year timeframe is reasonable and gives stakeholders time to comply with
the new requirements. A few comments noted that some parts of the rule
may require more than one year to implement and asked AMS to consider
this in the final rule. Few comments addressed the costs and benefits
of the rule in detail, but many comments noted in general that the
costs of the rule are acceptable and outweighed by the benefits.
AMS took these public comments into consideration when revising the
policy, implementation timeframe, and cost-benefit analysis of this
rulemaking. For more information on the comments received and AMS's
response to specific comments, refer to ``III. Overview of
Amendments.''
E. Terminology
Throughout this rule, AMS refers to four concepts--organic
integrity, organic fraud, audit trails, and supply chain traceability--
which are integral to the purpose of this rule. AMS is explaining these
concepts upfront to assist reader understanding:
Organic integrity: The unique attributes that make a
product organic and define its status as organic. A product that fully
complies with the USDA organic regulations has integrity, and its
organic qualities have not been compromised.
Organic fraud: Deceptive representation, sale, or labeling
of nonorganic agricultural products or ingredients as ``100 percent
organic,'' ``organic,'' or ``made with organic (specified ingredients
or food group(s))'' (7 CFR 205.2).
Audit trail: Documentation that is sufficient to determine
the source, transfer of ownership, and transportation of any
agricultural product labeled as ``100 percent organic,'' the organic
ingredients of any agricultural product labeled as ``organic'' or
``made with organic (specified ingredients)'' or the organic
ingredients of any agricultural product containing less than 70 percent
organic ingredients identified as organic in an ingredients statement
(7 CFR 205.2).
[[Page 3553]]
Supply chain traceability: The ability to identify and
track the movement, sale, custody, handling, and organic status of an
agricultural product along a supply chain. Supply chain traceability
audits are used to verify an agricultural product's compliance with the
USDA organic regulations.
F. Does this action apply to me?
You may be affected by this action if you are engaged in the
organic industry. Potentially affected entities may include, but are
not limited to, the following:
Individuals or business entities that are considering
organic certification;
Existing production and handling operations that are
currently certified organic under the USDA organic regulations;
Brokers, traders, and importers of organic products that
are not currently certified under the USDA organic regulations;
Operations that use non-retail containers for shipping or
storing organic products;
Retailers that sell organic products;
Operations that receive or review certificates of organic
operation to verify compliance with USDA organic regulations;
USDA-accredited certifying agents, inspectors, and
certification review personnel;
Operations that import organic products into the United
States; and/or
Operations that export organic products to the United
States and the corresponding certifying agents.
This list is not exhaustive but identifies key entities likely to
be affected by this action. Other types of entities may also be
affected. To determine whether you or your business may be affected by
this action, you should carefully examine the regulatory text and
discussion below.
G. Compliance Date
AMS is establishing a compliance date for this final rule of March
19, 2024, or 12 months after the effective date of this final rule.
This means that all entities affected by this rule, including certified
operations and certifying agents, must comply with the provisions of
this final rule by this date. This also means that operations requiring
organic certification because of this final rule must be certified by
the compliance date. AMS is setting this compliance date to allow
affected entities time to read and understand this final rule, obtain
organic certification if needed, and prepare for and implement other
changes in this final rule.
III. Overview of Amendments
A. Applicability and Exemptions From Certification
The table below includes the regulatory provisions related to this
section of the rule. A discussion of the policy follows.
------------------------------------------------------------------------
Section Final regulatory text
------------------------------------------------------------------------
205.2..................................... Terms Defined.
Definitions for Handle,
Handler, Handling
operation, and Retail
establishment.
205.100................................... What has to be certified.
Paragraph (a).
205.101................................... Exemptions from
certification.
Entire section.
205.310................................... Agricultural products
produced or processed by an
exempt operation.
Paragraphs (a) and (b).
------------------------------------------------------------------------
The USDA organic regulations require organic certification of
businesses that sell, process, or package organic agricultural products
as handling operations. This rulemaking clarifies that most operations
that operate in the middle of organic supply chains must be certified
organic. This may include entities that sell, trade, distribute, or
import organic products. The activities of these operations may affect
organic integrity; therefore, certification is necessary to assure
consumers that organically produced products meet a consistent
standard. In addition to clarifying who needs certification, this
rulemaking also provides limited exemptions to organic certification
for certain entities and activities that present a low risk to organic
integrity.
This action may affect noncertified operations that handle organic
products, sell organic products, or facilitate the sale or trade of
organic products on behalf of a seller or oneself; certified organic
operations; organic inspectors; and certifying agents. Readers should
carefully examine the regulatory text and policy discussion to
determine if they are affected.
Background
The organic market has grown considerably since the USDA organic
regulations took effect in 2002. The Organic Trade Association reports
that total U.S. organic sales grew from $3.4 billion in 1997 to $61.9
billion in 2020.\11\ This growth has created increasingly complex
organic supply chains as additional domestic and international
businesses choose to produce and sell organic products for the U.S.
market. Some segments of organic supply chains remain uncertified under
current regulation, creating gaps in oversight, increasing the
opportunity for fraud, and complicating enforcement by the USDA and its
enforcement partners.
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\11\ Organic Trade Association, Organic Industry Survey, 2018-
2021
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Oversight and enforcement of organic supply chains are challenging
because organic products are credence goods, which means that their
organic attributes, or ``integrity,'' cannot be easily verified by an
individual. Guaranteeing organic integrity requires transparent supply
chains, trusted interactions between businesses, and mechanisms to
verify product legitimacy. This is best accomplished via certification,
which requires operations to follow traceability and verification
practices, and provides regular oversight in the form of audits and
annual inspection. This rulemaking broadens the scope of who must be
certified, opening more of the organic supply chain to oversight and
mitigating the risks of noncertified businesses handling organic
product.
OFPA authorizes the USDA to regulate and enforce the production,
handling, and sale of organic products (7 U.S.C. 6503). This includes
activity within organic supply chains, from production through final
sale to the
[[Page 3554]]
consumer.\12\ AMS is exercising its authority to regulate entities in
organic supply chains by requiring certification of some types of
currently noncertified operations. This action is mandated by the 2018
Farm Bill, which states that the USDA must ``issue regulations to limit
the type of organic operations that are excluded from certification
under section 205.101'' of the organic regulations.\13\ This rulemaking
supports the OFPA's purpose ``to assure consumers that organically
produced products meet a consistent standard (7 U.S.C. 6506(a)(11)).''
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\12\ OFPA and the USDA organic regulations do not provide
authority to regulate the transport of organic agricultural
products.
\13\ See section 10104(a) of the Agriculture Improvement Act of
2018, Public Law No: 115-334, available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf,
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Who needs to be certified?
Section 205.100(a) of the organic regulations states that any
operation that produces or handles organic agricultural products must
be certified organic. This means that operations conducting activities
described in the definition of handle must be certified organic and
must follow all applicable portions of the OFPA and the USDA organic
regulations. In general, handle means to ``sell, process, or package''
organic agricultural products. Limited exemptions for operations that
handle organic agricultural products are described in Sec. 205.101(a)-
(h).
The definition of handle includes the term processing, which is
defined in Sec. 205.2.\14\ Operations that process organic
agricultural products must be certified. Handle further explains what
to ``sell'' and ``package'' mean by including additional examples of
handling activities. The examples represent typical supply chain
activities that may affect organic integrity. This includes activities
where there is physical contact with agricultural products, such as
combining, aggregating, culling, conditioning, treating, packing,
containerizing, repackaging, labeling, storing, receiving, or
loading.\15\ Examples of operations that often conduct these activities
may include grain elevators; bulk grain handlers; warehouses that cull,
label, or repackage; central bakeries or kitchens that serve grocery
chains; or ports of entry.
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\14\ 7 CFR 205.2 Processing. Cooking, baking, curing, heating,
drying, mixing, grinding, churning, separating, extracting,
slaughtering, cutting, fermenting, distilling, eviscerating,
preserving, dehydrating, freezing, chilling, or otherwise
manufacturing and includes the packaging, canning, jarring, or
otherwise enclosing food in a container.
\15\ The regulations at Sec. 205.2 define ``label'' and
``labeling'' to explain the type and location of information
covered. Labeling as a handling activity refers to the act of
applying a label to a product with an organic claim; applying other
types of labels, such as for inventory or information accompanying a
product, may not need certification.
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Handle also includes activities where there may not be physical
contact with agricultural products, such as selling, trading,
facilitating sale or trade on behalf of a seller or oneself, importing
to the United States, or exporting from a foreign country for sale in
the United States. These activities are included in the definition of
handle because they have the potential to affect organic integrity.
Operations that conduct these activities must be certified (unless
exempt per Sec. 205.101). Examples of operations that often conduct
these activities may include sales brokers, commodity traders,
ingredient sourcers, importers, or exporters.
The definition of handle is not an exhaustive list of activities
that must be certified. There may be additional activities not listed
in the definition that are similar to the listed activities and require
certification, or different words or synonyms for the same or similar
activities. The absence of a specific term in the definition of handle
does not mean the activity is not handling or that an operation
conducting this activity does not need certification.
What are the certification requirements for handlers?
All certified organic operations must follow the portions of the
USDA organic regulations that apply to activities they conduct.
Conversely, some portions of the regulation will not apply to every
operation (e.g., a certified operation that only produces crops does
not have to follow the livestock requirements of subpart C). Similarly,
the scope of a handling operation's certification only covers the
activities it conducts. For example, the OSP of a certified importer
would likely describe the operation's system to maintain transaction
records and audit trails, verify suppliers and NOP Import Certificates,
and verify traceability. On-site inspection of such an operation would
likely focus on a records review and evaluation, rather than evaluation
of physical facilities.
Contractors are sometimes used in the organic industry to provide
services to certified operations. Contractors that qualify for an
exemption per Sec. 205.101(a)-(f) do not need to be certified. Any
contractor performing handling activities on behalf of an operation
must be certified or described in the OSP of a certified operation.
It is common for some operations to handle both organic and
nonorganic agricultural products (i.e., a split operation). For a split
operation, only the portion(s) of the operation that produces or
handles organic agricultural products must be certified. If a portion
of an operation qualifies for an exemption from certification described
in Sec. 205.101(a)-(h), only that portion may be exempt, and the
remainder of the operation must be certified if it produces or handles
organic agricultural products. For example, a grocery store chain's
retail locations may be exempt under Sec. 205.101(b) or (c), but its
importing and some distribution activities would likely need to be
certified.
Organic Agricultural Products Received From an Exempt Operation
Agricultural products produced or processed on an exempt operation
must follow all requirements of Sec. 205.310. This means that an
operation receiving products produced or processed by an exempt
operation cannot represent the products as certified organic, cannot
display the USDA organic seal on the products, and cannot use the
products as organic ingredients in a product produced by the receiving
operation. In effect, product received and then processed by an exempt
operation loses its certified organic status and cannot be represented
as organic.
However, exempt operations may perform limited handling of
certified organic products, as described in each exemption at Sec.
205.101; i.e., if an exempt operation handles certified organic
products in a manner consistent with its applicable exemption, the
products maintain their organic status. This means, for example, that
an exempt warehouse may receive, store, and prepare for shipment
packaged certified organic products. Conversely, if this warehouse
opens or relabels such packaged products, then the certified organic
status of the products is lost, and an operation receiving these
products must not represent them as certified organic.
The USDA organic regulations require certified operations to
implement recordkeeping and verification practices that ensure the
integrity of organic agricultural products they receive, including
products received from exempt or uncertified operations. Records must
trace organic products back through any exempt operations to the last
certified operation in the supply chain, and operations must verify
their suppliers, including exempt operations. See Sec. Sec.
205.103(b)(2) and 205.201(a)(3) in the section on Supply Chain
Traceability and Fraud Prevention later in this rule.
[[Page 3555]]
Exemptions From Certification
The USDA organic regulations require certification of any operation
that produces or handles organic agricultural products (Sec.
205.100(a)). However, the regulations provide limited exemptions to
certain types of operations that conduct low-risk activities, and are
therefore less likely to compromise organic integrity of the
agricultural products they handle. These exemptions, and the conditions
that must be met to qualify for each, are described in Sec. 205.101.
The USDA organic regulations formerly used the terms ``exemption''
and ``exclusion'' to describe activities that do not require organic
certification. This final rule removes use of the term ``exclusion''
from Sec. 205.101 and throughout the organic regulation to reduce
confusion and misinterpretation about who needs to be certified. The
term ``exemption'' is now used exclusively to describe activities that
do not require organic certification. Previous ``exclusions'' listed
under former Sec. 205.101(b) have been modified and are now listed
under current Sec. 205.101.
Responsibilities of Exempt Operations
Operations described in Sec. 205.101 are exempt from the
requirement to be certified organic under subpart E. However, these
exempt operations must still follow all other applicable portions of
the organic regulations, including the production and handling
requirements of subpart C. For example, a very small vegetable farm may
be exempt from certification per Sec. 205.101(a); this means the farm
does not have to be certified and inspected annually, and does not have
to develop and submit an organic system plan. However, the farm must
follow the other organic production and handling requirements of
subpart C, including soil and fertility practices, crop rotation, weed
management, and seed use practices. Exempt operations must also comply
with Sec. 205.272 and practices to prevent commingling and contact
with prohibited substances.
Exempt operations must also follow the applicable labeling
requirements of subpart D. Critically, this means exempt operations
must not represent the agricultural products they produce or process as
certified organic and must not use the USDA organic seal. Additionally,
agricultural products produced or processed by an exempt operation must
not be identified or represented as organic in a product processed by
another operation (See Sec. 205.310, Agricultural products produced or
processed on an exempt operation). Additionally, exempt operations are
only permitted to perform the limited handling activities described in
the applicable exemption; any handling outside of that described in the
exemption may result in loss of organic status of products.
Operations that qualify for an exemption may voluntarily choose to
become certified. By becoming certified, the operation may market the
products it produces and processes as certified organic, display the
USDA organic seal on its products, and represent these products as
ingredients for use in other organic products.
Like certified operations, exempt operations are subject to
penalties for violating the OFPA and the organic regulations. Section
205.100(c) of the organic regulations states that any person or
responsibly connected person--including exempt operations--that
knowingly sells or labels a product as organic, except in accordance
with the Act, shall be subject to a civil penalty as specified in 7 CFR
3.91(b)(1)(xxxvi).\16\
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\16\ 7 CFR 3.91(b)(xxxvi): Civil penalty for knowingly labeling
or selling a product as organic except in accordance with the
Organic Foods Production Act of 1990, codified at 7 U.S.C. 6519(c).
As of the publication of this rule the civil penalty amount is a
maximum of $20,130 per violation.
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Recordkeeping by Exempt Operations
Like certified operations, exempt operations play a critical role
in maintaining the integrity of organic products as they travel from
production to consumer. Therefore, exempt operations must maintain
records of the organic products they produce and handle, including
records that: demonstrate that agricultural products identified as
organic were organically produced and handled; and verify quantities of
organic agricultural products received and shipped or sold. Such
records are necessary to maintain an audit trail for organic products;
this will facilitate many other provisions of this rule, including
supply chain traceability audits (Sec. 205.501(a)(21)), recordkeeping
by certified operations (Sec. 205.103), on-site inspections (Sec.
205.403(d)), and fraud prevention plans (Sec. 205.201(a)(3)). Retail
establishments that do not process agricultural products (see
definition for Handle at Sec. 205.2 and exemption from certification
at Sec. 205.101(b)) do not need to maintain such records. Exempt
handlers must have required records available and must show those
records to a representative of the Secretary upon request. Failure to
produce compliant records may lead to enforcement action.
Small Producers and Handlers
Small organic producers and handlers are exempt from certification
at Sec. 205.101(a). This exemption is limited to producers and
handlers with gross agricultural income from organic sales of no more
than $5,000 annually. These operations are exempt from certification
under subpart E and from submitting an organic system plan, but must
follow all applicable organic production and handling requirements of
subpart C and labeling requirements of subpart D. This includes the
requirements to prevent commingling and prevention of contact with
prohibited substances (Sec. 205.272).
Such operations must not represent the agricultural products they
produce or process as certified organic and must not use the USDA
organic seal. Agricultural products produced or processed by these
exempt operations must not be identified or represented as organic in a
product processed by another operation (see Sec. 205.310).
Retail Establishments
Retail businesses that handle organic agricultural products and
sell directly to consumers may be exempt from certification. To qualify
for an exemption, the operation must be a retail establishment and meet
the conditions for the exemptions in Sec. 205.101(b) and (c).
The regulations define retail establishment to include a range of
transaction modes for selling to consumers that commonly occur in the
modern marketplace. Retail establishment includes restaurants,
delicatessens, bakeries, grocery stores, or any retail business with a
restaurant, delicatessen, bakery, salad bar, bulk food self-service
station, or other eat-in, carry-out, mail-order, or delivery service of
raw or processed agricultural products. Retail is commonly described as
selling directly to consumers, end-users, or the public. The definition
for retail establishment aligns with that concept. Businesses which
sell to other businesses (wholesale) do not qualify as retail
establishments. Retail establishments may use virtual transactions for
sales, but they must also have a physical location for consumers to
purchase products.
Only operations that are retail establishments are eligible for the
retailer exemptions. The definitions for handler and handling operation
do not include final retailers of agricultural products that do not
process agricultural products. This exemption from certification is
also reinforced at section 205.101(b), which exempts retail
establishments that sell, but do not
[[Page 3556]]
process, organic agricultural products to consumers.
Section 205.101(c) exempts retail establishments that process
certified organic agricultural products at the point of sale to the
consumer. Distributors or brand name owners that do not qualify as
retail establishments should review the exemptions from certification
at Sec. 205.101(e) and (f), as those may apply to their activities.
Retail Operations That Don't Process
Retail establishments that do not process agricultural products are
not handlers or handling operations and may be exempt from
certification under Sec. 205.101(b). The OFPA and Sec. 205.2 define
processing as cooking, baking, heating, drying, mixing, grinding
churning, separating, extracting, cutting, fermenting, eviscerating,
pre-serving, dehydrating, freezing, or otherwise manufacturing, and
includes the packaging, canning jarring, or otherwise enclosing food in
a container. A retail establishment that is not processing may do other
handling activities without certification. This could include, for
example, removing produce from shipping boxes and washing and
transferring product to display cases or opening bags of oats and
transferring contents to bulk food dispensers. Although a retailer
performing such handling activities may be exempt from certification,
all retail establishments must comply with Sec. 205.272, which
requires measures to prevent commingling of organic products and
contact with prohibited substances.
Retail establishments that do not process ``100% organic'' and
``organic'' unpackaged products may use the USDA organic seal and/or
seal of the certifying agent in retail labeling and display of these
unpackaged products (Sec. 205.308). Retail establishments that do not
process ``made with organic. . .'' unpackaged products may use that
claim in retail labeling and displays (Sec. 205.309).
Retail Establishments That Process
Retail establishments that process organic agricultural products
may be exempt from certification under Sec. 205.101(c). To qualify for
this exemption, a retail establishment must process organic products at
the point of final sale to the consumer. This means that the products
must be processed and sold in the same physical location. This could
include repackaging bulk containers of organic product into individual
units for retail sale within an individual grocery store or a retail
establishment that prepares ready-to-eat meals and sells them online to
consumers from the processing location.
Per Sec. 205.310, organic agricultural products that are processed
by exempt retail establishments (such as in the examples above) must
not be sold, labeled or represented as ``certified'' organic, must not
display the USDA seal or identify the certifying agent, and must not be
used by another operation as ingredients in a certified organic
product. Only retail establishments that are certified organic may use
the USDA organic seal (or make certified organic claims) on products
they process.
This exemption does not cover retail establishments that sell
organic products to consumers which are processed at a location
separate from the point of sale. This could include, for example, an
online retailer that sells products processed at an uncertified
facility or a central processing facility that prepares food sold in
bakery and deli sections of grocery stores. In these scenarios, the
processing facility is not co-located in the same physical location as
the point of sale and the retail establishment exemption does not cover
separate processing facilities. The processors would need to be
separately certified in order for a retail establishment to sell their
products as organic.
In addition, this exemption does not cover retailers that process
and sell to consumers only via virtual transactions. ``Virtual
transaction'' describes any form of transaction that does not occur in-
person (e.g., telephone, mail-order, and/or online sales). Retailers
that process and sell to consumers virtually without having a physical
location for retail sales must be certified. These businesses do not
meet the definition for retail establishment, and, by extension, the
conditions for exemption from certification.
All exempt retail establishments must comply with the requirements
of Sec. 205.272, which describes handling requirements to prevent
commingling and contact with prohibited substances. In addition, exempt
retail establishments that process organic products must follow the
labeling provisions specified in Sec. 205.310 and maintain records to
(1) demonstrate that agricultural products identified as organic were
organically produced and handled; and (2) verify quantities received,
sold, or produced from such agricultural products. Exempt handlers must
have these records available and must show them to a representative of
the Secretary upon request (7 U.S.C. 6519(a)(1)). Failure to produce
compliant records may lead to enforcement action.
Operations That Handle Only Products With Less Than 70 Percent Organic
Ingredients
Section 205.101(d) exempts from certification operations that only
handle agricultural products with less than 70 percent organically
produced ingredients, and operations that only identify organic
ingredients on the product informational panel. This exemption is not
new policy. It combines two existing exemptions: operations that handle
products with less than 70 percent organic ingredients (former Sec.
205.101(a)(3)) and operations that handle products that only identify
organic ingredients on the information panel (former Sec.
205.101(a)(4)). AMS combined these exemptions because they cover
operations that handle products in the same labeling category (per
Sec. 205.305), and because these operations must follow identical use
and labeling requirements. Operations that qualify for this exemption
are exempt from certification under subpart E and from submitting an
organic system plan, but must follow all applicable organic production
and handling requirements of subpart C and labeling requirements of
subpart D. This includes the labeling requirements for products with
less than 70 percent organic content (Sec. 205.305) and the
requirements to prevent commingling and prevention of contact with
prohibited substances (Sec. 205.272).
Handlers covered under this exemption must have the records
required by Sec. 205.101(i) available and show them to a
representative of the Secretary upon request (7 U.S.C. 6519(a)(1)).
Failure to produce compliant records may lead to enforcement action.
Such operations must not represent the agricultural products they
produce or process as certified organic and must not use the USDA
organic seal. Agricultural products produced or processed by these
exempt operations must not be identified or represented as organic in a
product processed by another operation (see Sec. 205.310).
Storing or Selling Packaged Organic Products
The movement of packaged and sealed organic products through the
supply chain is a lower-risk activity. Packaged products are less
likely to be commingled, exposed to contaminants, or tampered with, and
alterations are easier to detect. Handling operations that sell,
distribute, or store packaged organic agricultural products may be
exempt from organic certification. Two exemptions, at Sec. 205.101(e)
and (f),
[[Page 3557]]
apply to limited handling activities involving only organic
agricultural products that are in sealed, tamper-evident packaging or
containers. The key distinctions between these exemptions are that
205.101(f) covers operations that buy and sell, in addition to
receiving, storing and/or preparing for shipment, and that 205.101(f)
covers only retail-packaged products versus packaged products that are
not in final retail packaging. Tamper-evident packaging or container
means that the contents are sealed in a manner where an attempt to
break the seal, access the contents, or reclose the package would be
obvious. These exemptions cover only the specified handling activities.
These exemptions do not, for example, cover buying, selling, receiving,
storing, or loading of unpackaged products; those activities require
certification.
The exemption at Sec. 205.101(e) is intended primarily for storage
and warehouse facilities. Section 205.101(e) applies to handlers that
are only receiving, storing and/or preparing for shipment products that
are received in and remain in sealed, tamper-evident packaging until
the products leave their custody. This allowance may cover, for
example, warehouses and storage facilities, including some cold storage
facilities that only receive and store packaged products and prepare
them for shipment to another entity. Examples of tamper-evident
packaging include produce boxes with ``DO NOT TAMPER WITH'' tape placed
across the box flaps, sealed bulk bags of flour, or sealed drums and
totes of olive oil. Storage facilities or warehouses that receive
products that are not in sealed, tamper-evident packaging must be
certified.
The exemption at Sec. 205.101(f) is intended primarily for
distributors. Section 205.101(f) applies to handlers that only buy,
sell, receive, store and/or prepare for shipment retail-packaged
organic agricultural products. This allowance may cover, for example,
some distributors, brand name owners, and sales brokers that purchase
and/or receive products in their finished retail packaging. Products
must be received in and remain in the final retail packaging without
alteration throughout their custody. This exemption does not apply to
sales brokers, traders, or other handlers that buy and sell products
that are not in their final retail packaging.
Preparing for shipment is an activity that is covered under both
exemptions at Sec. 205.101(e) and (f). This may include various tasks
that must be performed with the sealed, tamper-evident packaging
remaining intact and without altering product contents or any retail
labeling. Examples of preparing for shipment include putting packaged
products into shipping containers, applying internal tracking numbers,
shrink-wrapping shipping cartons to a pallet, breaking down pallets of
fully packaged products, adding protective packaging to nonretail
containers or retail displays of organic products, packing individual
packaged products onto a shipping pallet, loading/unloading packaged
products onto or from transport vehicles, and placing individual retail
packages into a retail display which the certifying agent of the last
certified handling operation has verified as compliant.
Handlers that qualify for an exemption at Sec. 205.101(e) or (f)
must use practices for preventing commingling and contamination of
organic products, in compliance with Sec. 205.272. In addition, exempt
handlers must have records available and must show those records to a
representative of the Secretary upon request, to show that organic
products are organically produced and handled and to verify quantities
of organic product received and shipped or sold. Failure to produce
compliant records may lead to enforcement action.
Customs Brokers
Section 205.101(g) exempts Customs brokers from organic
certification. Customs brokers facilitate the entry of products into
the United States by helping meet import documentation and filing
requirements and by acting as intermediaries between importers and the
U.S. government. Customs brokers do not take ownership or physical
possession of organic products and their actions present minimal risk
to organic integrity. They are often distinct from sales or commodity
brokers, who sell or facilitate the sale of organic products--those
operations must be certified if they handle organic products. Customs
brokers also play a critical role by filing NOP Import Certificate data
in the U.S. Custom and Border Protection's (CBP) Automated Commercial
Environment (ACE) import entry system.
This exemption is limited to Customs brokers as defined by 19 CFR
111.1: ``a person who is licensed under this part to transact customs
business on behalf of others.'' Customs business is further defined in
19 CFR 111.1 and includes ``activities involving transactions with CBP
[U.S. Customs and Border Protection] concerning the entry and
admissibility of merchandise . . . payment of duties, taxes, or other
charges . . . the preparation . . . of documents in any format and the
electronic transmission of documents . . . intended to be filed with
CBP in furtherance of any other customs business activity . . . '' \17\
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\17\ See 19 CFR 111.1 for complete definitions of Customs broker
and Customs business: https://www.ecfr.gov/cgi-bin/retrieveECFR?gp=&SID=ab6e30d35ef538ce07bc8021d6e1d4c3&mc=true&n=sp19.1.111.a&r=SUBPART&ty=HTML#se19.1.111_11.
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To qualify for this exemption, Customs brokers must only conduct
customs business. If a Customs broker conducts any additional activity
within the definition of handle--such as selling, importing, or
trading--the Customs broker must be certified.
Logistics Brokers
Section 205.101(h) exempts from certification operations that only
arrange for the shipping, storing, transport, or movement of organic
agricultural products. Sometimes known as ``logistics brokers,'' these
operations facilitate the movement and storage of agricultural products
by connecting a consigner (or consignee) with a carrier who can
transport/store the products. Logistics brokers do not take ownership
or physical possession of organic products. The activities they conduct
present minimal risk to organic integrity because they only secure
transport/storage to meet the needs of a third party who owns or is
responsible for the agricultural product.
This exemption is limited to operations that only arrange for the
shipping, storing, transport, or movement of agricultural products and
do not conduct any other activity in the definition of handle. If such
an operation conducts other handling activities--such as selling,
importing, or trading--the operation must be certified.
Transport
Transport of agricultural products alone is not a handling activity
and does not require certification (see definitions of handle in 7 CFR
205.2 and 7 U.S.C. 2502(8)). Transport generally refers to the movement
of products in commerce. Examples of activities which are
transportation and do not require certification include: moving organic
hay or milk from a certified producer to a certified organic buyer or
certified processing facility, moving organic grain or organic
livestock from certified organic farms to a certified handling or
slaughter facility, and food delivery services transporting prepared
foods from a retail establishment to a consumer.
Any activities other than the movement of product on a
transportation vehicle or moving products between transportation
[[Page 3558]]
vehicles (transloading) are handling and require certification.
Handling activities which are adjacent to transport require
certification unless they are covered by exemptions 205.101(e) or (f)
for packaged products. Examples of adjacent activities which do not
qualify as transport include combining, splitting, containerizing,
packing/repacking, treating, sorting, opening, enclosing, or labeling/
relabeling. In addition, loading or unloading of unpackaged products
into or from a storage facility is not a form of transportation; this
activity must be certified.
Certified operations are responsible for verifying that products
handled by uncertified entities in their supply chain remain in
compliance with the organic regulations. This includes verifying
organic products transported by an uncertified transporter. A certified
operation needs to describe procedures for verifying suppliers in the
supply chain and the organic status of products received (Sec.
205.201(a)(3)). In addition, certified operations must maintain records
back to last certified operation, which may encompass uncertified
operations that fall between certified entities (Sec. 205.103(b)(2)).
The certified organic operation responsible for the organic products
that are transported must: maintain records, for the audit trail and
traceability, in sufficient detail as to be readily understood and
audited; demonstrate prevention of commingling and contamination during
transportation (Sec. 205.272); fully describe the transportation
practices in the organic system plan; and ensure that the
transportation records for organic products are available for
inspection. Certified operations that load or receive products from
uncertified transporters can verify prevention of contamination/contact
with prohibited substances through, for example, affidavits or other
documentation of vehicle clean out.
Summary of Changes to the Final Rule
AMS made several revisions to the proposed regulatory text when
writing this rulemaking. Changes to the rulemaking are discussed below.
This is then followed by responses to specific themes from public
comment.
AMS revised the definition of handle to include additional
examples of activities that require organic certification. AMS added
these activities in response to public comments, which asked for
additional clarity about who must be certified. The additional
activities in the definition more clearly indicate activities that
require certification and will help businesses determine whether they
need organic certification.
AMS simplified the term handler and removed ``except for
operations that are exempt from certification'' and ``or a portion of
[an operation]'' from handling operation. These phrases are redundant
because they are explained in Sec. 205.100--What has to be certified.
AMS also added ``except final retailers of agricultural products that
do not process agricultural products'' to both definitions. This
clarifies that certain final retailers are not handlers or handling
operations and aligns the definitions with OFPA. The two definitions
are now mostly synonymous, differing only in their reference to either
a person or an operation.
The proposed rule would have replaced the defined term
retail food establishment with the updated term retail operation, which
focused on the key activities of retailers, notably those selling
``directly to final consumers.'' Many public comments noted that the
proposed phrase ``direct to final consumers'' was imprecise and would
not be interpreted consistently by stakeholders. These comments also
indicated that stakeholders are familiar with the meaning of the
original defined term retail food establishment and how to apply it.
Therefore, this final rule uses the defined term retail establishment,
which has language very similar to the original retail food
establishment, to ensure consistent stakeholder understanding. This
final defined term removes the word ``food'' because retailers
sometimes sell non-food items; it also avoids the potentially confusing
phrase ``directly to final consumers.'' Finally, this definition for
retail establishment adds more examples of types of retail
establishments to help stakeholders determine whether they are a retail
establishment.
AMS removed ``or a portion of an operation'' from the
descriptions of each exemption; this language was redundant because it
is included in Sec. 205.100--What has to be certified.
AMS removed references to Sec. 205.272 because they are
redundant to the reference to subpart C in the introductory paragraph
of Sec. 205.101.
In the introductory paragraph of Sec. 205.101, AMS
replaced references to Sec. 205.310 with a reference to subpart D.
This more broadly references the labeling requirements exempt
operations must follow, including use of the USDA seal and labeling in
retail environments.
In Sec. 205.101(b), AMS removed ``sells'' to clarify that
retail establishments may also perform some handling (not just selling)
in the regular course of business.
In Sec. 205.101(c), AMS removed the reference to
agricultural products ``previously labeled for retail sale'' and
replaced it with the statement ``certified under this part'' to clarify
that retailers may process certified organic products regardless of
whether the products are labeled for retail sale or for other use
(e.g., organic products labeled for food service).
AMS revised Sec. 205.101(e) to exempt only storage of
products sealed in tamper-evident packaging. Storage of unpackaged
organic products is a high-risk activity that requires certification to
maintain integrity. Sealed, tamper-evident packaging makes organic
products less susceptible to fraud and mishandling and helps maintain
organic integrity during storage and handling by uncertified
operations.
AMS added new paragraph (f) in Sec. 205.101 to exempt the
sale of retail products sealed in tamper-evident packaging. Sale of
this type of packaged retail products presents little risk to organic
integrity, and operations storing and selling these products do not
require organic certification.
AMS added new paragraphs (g) and (h) to Sec. 205.101 to
exempt Customs brokers and logistics brokers because these operations
only facilitate entry of imports into the United States, and their
activities do not present a risk to organic integrity.
AMS removed recordkeeping requirements from specific
exemptions and replaced them with a general ``Recordkeeping by exempt
operations'' paragraph at Sec. 205.101(i).
AMS revised Sec. 205.310 to remove ``or excluded'' and
replaced ``handled'' with ``processed'' to more clearly indicate that
products processed by an exempt operation must not be used as an
ingredient in an organic product processed by others.
Summary of Public Comment
AMS received many public comments from stakeholders across the
organic industry discussing this section of the proposed rule. The
majority of comments generally supported AMS's proposed revisions and
agreed that the organic regulations must clearly indicate who needs to
be certified and reduce the types of uncertified operations in organic
supply chain. Many commenters requested further clarification of the
proposed changes, particularly about the need for organic certification
and exemptions from certification.
[[Page 3559]]
Revised Definitions
The revised definition of handle was discussed in many comments.
Some commenters requested expanding the definition to include terms
such as ``port,'' ``transload,'' and ``brand owner'' to the regulatory
text. Commenters also requested specific distinctions be made between
``transport'' and ``transload,'' noting current inconsistency in how
these are interpreted by the industry.
Some comments discussed further clarification needed, including how
``cold storage'' fits into the rule. Other comments requested to
further clarify handle by better defining ``split.'' Another commenter
requested clarification for operations that repackage or repurpose
certified organic products for on-site sale (e.g., delis). A few
commenters also requested AMS discuss virtual transactions more
clearly.
In response to AMS's request for additional activities that may
need to be certified, commenters suggested the following be added to
the definition of handle: split, open, close, sort, combine,
consolidate, aggregate, enclose, condition, treat, size, grade,
transload, brand ownership, private label, import, export, commingle,
transport, and deliver.
Exemptions
Certification of and exemption for brokers was frequently discussed
in comments. Many commenters requested that brokering activities be
exempt, with some requesting broad exemptions for all brokers and
others favoring exemptions for certain brokering activities. These
comments explained that exemptions are warranted because brokers
typically do not take physical possession of the products. Many
commenters also stated that all brokering activity should be certified,
regardless of physical or financial possession.
Several comments requested changes or clarifications to the
exemption for operations with organic sales of less than $5,000,
although the proposed rule did not revise existing policy. Most of
these comments wrote in support of this exemption, though some proposed
changes such as raising the maximum receipts to $10,000 while still
maintaining exempt status.
In general, some comments requested fewer exemptions, and asked AMS
to implement a transition period for operations that would require
certification under the rulemaking. Further comments wrote that
operations that sell direct to consumers should be eligible for
exemption. Several comments requested that storage facilities which
only receive product packaged by a certified operation be exempt. One
comment requested that products, not operations, be eligible for
exemption because operations can interact with organic and non-organic
products.
Some comments also requested clarification about private label
brands. There was no clear consensus among comments about the need to
certify such operations. Many comments stated that these operations
must be certified, and that doing so would improve traceability and
integrity. Others requested that private labels be exempt to avoid
additional costs and labeling inconsistencies. Further comments
requested that ``private label'' be added to the definition of ``retail
establishment'' because retail brands often sell private-labeled
product.
Comments disagreed about the specific requirements exempt
operations must follow. Some comments argued for more specific
regulatory requirements for exempt operations (i.e., clarify what
exempt operations can and cannot do). Many comments discussed the use
of the USDA organic label by exempt operations, stating that exempt
operations should not be permitted to use the certified organic label.
They requested that whenever the organic label is used, the business
must be certified.
Transport
Many comments requested specific exemptions for most transportation
of organic products. Specifically, several comments requested that milk
hauling and transportation between two certified operations should be
exempt from certification. While the majority of comments requested
these types of transportation be exempt, some comments disagreed,
requesting limits on transportation exemptions. Other comments
requested clarification for whether third-party delivery services that
restaurants use are exempt. Finally, some comments also asked AMS to
clarify whether transloading activities need to be certified.
Recordkeeping and Compliance
Some comments were concerned with verifying exempt operations
compliance. Several commenters suggested requiring universal use of
affidavits when doing business with exempt operations. Another
suggested utilizing invoices to track compliance using mass-balance
audits.
Many comments addressed recordkeeping. Several comments requested
modifying recordkeeping requirements to require exempt operations to
maintain records for five years to align requirements for certified and
exempt operations. Other comments wrote that the recordkeeping
requirements are burdensome for exempt businesses and asked AMS to not
require certain recordkeeping practices.
Responses to Public Comment
Definition of Handle
(Comment) AMS received many comments about the definition of handle
and activities that should or should not require certification.
Comments discussed a wide range of activities spanning all segments of
the supply chain and suggested many additional activities to include in
the definition of handle, including to split, open, close, sort,
combine, consolidate, aggregate, enclose, condition, treat, size,
grade, transload, brand ownership, private label, import, export,
commingle, transport, and deliver. Conversely, comments also provided
examples of activities that should not require certification, including
storing packaged products, transporting, delivering, repackaging or
splitting cases of retail-packaged products, loading, receiving,
brokering, selling or trading packaged products, selling retail
products, or labeling for inventory purposes.
(Response) AMS agrees that some of the activities presented by
commenters require certification and has added more examples to the
definition of handle to help clarify who and what activities must be
certified. The definition of handle is not an exhaustive list of
activities that must be certified. There may be additional activities
not listed in the definition that require certification, or different
words or synonyms for the same or similar activities. The absence of a
specific term in the definition of handle does not mean the activity is
not handling or that an operation conducting this activity does not
need certification. More specific responses to certain activities are
discussed below.
(Comment) Several comments noted the difference between the
definitions of handler and handling operation and asked AMS to either
clarify this difference, or harmonize the two definitions.
(Response) AMS simplified handler and removed ``except for
operations that are exempt from certification'' and ``or a portion of
[an operation]'' from handling operation. These phrases are redundant
because they are explained in Sec. 205.100--What has to be certified.
AMS also added ``except final retailers
[[Page 3560]]
of agricultural products that do not process agricultural products'' to
both definitions. This clarifies that certain final retailers are not
handlers or handling operations, and aligns the definitions with OFPA.
The two definitions are now mostly synonymous, differing only in their
reference to either a person or an operation.
(Comment) Several comments asked AMS to include importing and
exporting to the definition of handle, noting that the mandatory use of
NOP Import Certificates requires certification of importers and
exporters.
(Response) AMS agrees with these comments and has added importing
to the United States and exporting for sale in the United States to the
definition to help clarify that these activities require certification,
and to support the mandatory use of NOP Import Certificates described
in Section 2 of this rule, Imports to the United States.
(Comment) Commenters questioned the inclusion of ``facilitating
sale or trade'' in the definition for handle. The comments explained
that the meaning is vague and too broad and would result in customs
brokers, freight forwarders, sales brokers, and administrative
activities requiring certification.
(Response) The original definition for handle covered many
activities in the supply chain, from post-production to retail sale.
The updated definition is specific about which activities are included
in ``sell, process or package.'' However, the list of activities is not
exhaustive and does not capture all activities that may be considered
as selling, processing, or packaging an agricultural product. AMS
included ``facilitating sale or trade on behalf of a seller or
oneself'' as a general category to capture activities which are
integral to selling a product and may be known by various names. The
definition for handle includes handling activities that fall under
AMS's authority, although sometimes certain activities listed in handle
may not require certification. For example, entities that perform lower
risk activities--such as Customs brokers, logistics providers (e.g.,
freight forwarders), and limited handling of packaged products--may be
exempt from certification (see Sec. 205.101(e)--(h)).
Retail
(Comment) AMS received comments requesting clarification regarding
whether distribution centers and transport vehicles associated with a
retail establishment are exempt from certification. Some commenters
requested that off-site warehouses and distribution centers not be
exempt unless they meet proposed Sec. 205.101(e). According to
commenters, this clarification is needed to ensure that distribution
centers do not avoid certification by claiming to be an exempt retail
establishment.
(Response) A warehouse or distribution center associated with a
retail establishment is only exempt if it meets the criteria described
in Sec. 205.101(e) or (f). Transport vehicles associated with a retail
establishment do not require certification if they only transport and
do not handle organic agricultural products per Sec. 205.2.
(Comment) AMS received comments asking whether virtual transactions
with a final consumer are exempt from certification. Although a few
comments asked NOP to either exempt or require certification of this
activity, most comments did not give an opinion and only asked NOP for
clarification.
(Response) AMS has provided additional clarification by noting that
only businesses that meet the definition for retail establishment are
exempt under Sec. 205.101(b) and (c). Virtual businesses that only
sell retail packaged products to consumers, but do not qualify as
retail establishments, may be exempt from certification if they meet
the criteria of Sec. 205.101(f). AMS provides further detail in the
``Retail establishments'' section of the preamble.
(Comment) Comments noted that the proposed definition of retail
operation did not include the list of examples that was provided in the
preamble, and asked AMS to add them to the definition.
(Response) AMS agrees that the examples help clarify the definition
and has added them to the final definition of retail establishment.
(Comment) Comments requested revising the exemption for retailers
that process by not limiting this to processing only products that were
previously labeled for retail sale. Comments indicated that retailers
commonly source products labeled for food service.
(Response) AMS has removed that qualification from Sec. 205.101(c)
to clarify that exempt retail establishments may process certified
organic products regardless of whether the products are labeled for
retail sale.
(Comment) AMS received comments asking about the status of food
delivery services, specifically those affiliated with or serving retail
operations. Although a few comments asked NOP to either exempt or
require certification of this activity, most comments did not give an
opinion and only asked NOP for clarification.
(Response) Services which deliver products from a retail
establishment to a consumer may not require certification. A service
which delivers product from the retailer to the consumer after final
sale and does not engage in handling is transport and does not require
certification.
(Comment) Comments requested clearer guidance on what handling
activities retail operations could engage in and remain exempt.
Comments explained that the exemption for retailers that only sell and
retailers that process creates uncertainty for the many retail
operations that sell and handle. A few comments gave specific examples
of activities that exempt retail establishments should be allowed to
conduct, including removing/unpacking products, washing and
transferring products to retail displays, and breaking down master
cases of individual packaged products. However, most comments did not
give an opinion and only asked NOP for clarification.
(Response) AMS has revised the definitions of handler and handling
operation to exclude retailers that do not process organic agricultural
products; these operations may not require certification. This is
reinforced by the exemption for retailers that handle but do not
process at Sec. 205.101(b), which acknowledges that exempt retail
establishments may perform some handling activities. AMS has also
revised the definition for handle to be more specific about the types
of activities included. The additional description will help to clarify
the differences and overlap in handling and processing activities.
(Comment) Comments asked to clarify the meaning of ``point of
sale'' in reference to virtual transactions for retailers. There was a
suggestion to allow virtual transactions only when the sale occurs from
a brick-and-mortar retail location, to prohibit retailers that sell
only via an online platform.
(Response) The definition for retail establishment allows for
virtual retail transactions. For a retail establishment to be exempt,
the sales must occur at the same location as the processing, and there
must also be a physical location for consumers to purchase products.
Storage
(Comment) AMS received comments stating that storage of unpackaged
or bulk organic products is high-risk and should require certification.
They also noted that the proposed rule eliminated the distinction
between packaged and unpackaged product relating to receiving, storing,
and loading activities; this could allow high-risk operations
[[Page 3561]]
such as grain elevators and ports of entry to be exempt from
certification. Some comments requested AMS only exempt the storage of
sealed, tamper-evident packaged products.
(Response) AMS has revised the exemption at Sec. 205.101(e) to
exempt only operations that store, receive, and prepare for shipment
organic products in sealed, tamper-evident packages. Products must
remain in their packages and the exempt operation must not handle the
product beyond storing, loading, and preparing for shipment. Operations
that store bulk products or products not packaged in sealed, tamper-
evident packaging must be certified.
AMS made this change because the proposed rule would have exempted
operations that store unpackaged or bulk organic products. Many public
comments noted that storage of unpackaged organic products is a high-
risk activity that requires certification to maintain integrity. AMS
agrees that storage of unpackaged products is a high-risk activity.
Lack of sealed or protective packaging increases the likelihood of
contamination with prohibited materials (e.g., pesticides and
fumigants), commingling with nonorganic products, and
misidentification. These risks are especially great in high-activity
areas, and storage of unpackaged products requires additional care and
oversight to ensure organic integrity is maintained. Therefore, AMS is
requiring certification of operations that store unpackaged products.
Conversely, because packaging reduces the risk of contamination,
commingling, and misidentification, AMS is granting an exemption from
certification for operations that only store packaged products that are
sealed upon arrival and remain in their packaging.
AMS has narrowed the exemption to include only operations that
store, receive, and/or prepare for shipment organic products in sealed,
tamper-evident packaging. Sealed, tamper-evident packaging makes
organic products less susceptible to fraud and mishandling and helps
maintain organic integrity during storage and handling by uncertified
operations.
(Comment) Commenters requested AMS exempt from certification
activities where packaged product remains in its container, such as
breaking up pallets of packaged organic products that remain in its
original inner packaging, or placing such products into a retail
display.
(Response) Section 205.101(e) and (f) exempt operations that
receive, store, and prepare for shipment organic products enclosed in
sealed, tamper-evident packages or containers. Preparing for shipment
may include various tasks that must be performed with the sealed,
tamper-evident packaging remaining intact and without altering product
contents or any retail labeling. Examples of preparing for shipment
include putting packaged products into shipping containers, applying
internal tracking numbers, shrink-wrapping shipping cartons to a
pallet, breaking down pallets of fully packaged products, adding
protective packaging to nonretail containers or retail displays of
organic products, packing individual packaged products onto a shipping
pallet, placing individual retail packages into a retail display, and
loading/unloading packaged products onto or from transport vehicles.
(Comment) Several comments asked if cold storage of organic
agricultural products is exempt from certification, pointing to the
inclusion of ``chilling'' in the definition of processing.
(Response) Cold storage of organic agricultural products may be
exempt from organic certification if the activity meets the criteria of
Sec. 205.101(e), i.e., only sealed, tamper-proof packaged organic
products are stored. The act of cooling packaged organic products is a
common low-risk storage activity that is different from ``chilling''
performed as part of organic product processing.
(Comment) Several commenters requested that AMS remove the verb
``loads'' from proposed Sec. 205.101(e) for operations that storage
organic products, arguing that ``load'' could be conflated with
handling activities such as placing or packaging bulk products into
containers.
(Response) AMS uses ``prepare for shipment'' in exemptions at Sec.
205.101(e)-(f) to clarify that these exempt operations may not perform
activities such as packaging or loading bulk products into containers.
Prepare for shipment means that these operations may move products into
or onto a mode of transport, provided that the products are packaged
per Sec. 205.101(e)-(f).
(Comment) One commenter asked AMS to require certification of
storage facilities that store both organic and nonorganic agricultural
products. They argue that such ``split'' storage operations are a known
source of contamination and commingling, and that certification is
necessary to prevent this.
(Response) This rulemaking addresses the risks of contamination and
commingling by split storage operations by (1) requiring the
certification of operations that handle unpackaged organic products and
(2) limiting the exemption for storage operations to only those that
handle sealed, tamper-proof packaged organic products. AMS believes
these changes will mitigate the risks of split operations.
Additionally, Sec. 205.100(a) states that ``each operation or
portion of an operation'' that handles organic agricultural products
must be certified. Similarly, the exemption at Sec. 205.101(e), which
allows storage of packaged organic products without certification,
would be limited to only the portions of an operation that meet the
narrow criteria of this exemption. This means that a portion of a split
operation that stores unpackaged organic products needs to be
certified.
Transport
(Comment) Commenters requested that AMS explicitly state what
transportation activities are exempt from certification. They also
noted that the regulatory text and preamble lack a specific exemption
for transport of agricultural products.
(Response) The OFPA provides AMS authority to regulate the handling
(i.e., selling, processing, or packaging) of organic agricultural
products; however, transportation activities are not included in this
authority. Transport is generally described as the movement of products
in commerce. Based on the OFPA, transport of organic agricultural
products does not need to be certified; however, any handling
activities that occur during transport must be. See the definition of
handle for examples of activities that may require certification.
(Comment) AMS received several comments asking if milk haulers will
require organic certification. Most comments requested only
clarification on this topic, but several specifically requested that
milk haulers be exempted from certification.
(Response) AMS is defining the need for certification based on
activities performed, not type of business, because this will ensure
that businesses conducting high-risk activities require certification
(and conversely that businesses that conduct low-risk activities remain
exempt). A milk hauler would be exempt from certification if they only
transport organic milk (e.g., move milk from a dairy to a processor)
but do not otherwise handle the milk (e.g., process or package loads of
milk). Transport alone does not require certification.
(Comment) AMS received comments requesting that the transport
exemption be limited to transport from one certified operator to
another, or to a
[[Page 3562]]
final retailer, to ensure traceability of product throughout supply
chains.
(Response) AMS is not restricting transport of organic agricultural
products from one certified operation to another. This rule ensures
traceability via other means: certified operations must maintain audit
trail documentation for products they produce or handle (Sec.
205.103(b)(3)) and keep records to trace organic products received back
to the last certified operation in the supply chain (Sec.
205.103(b)(2)). This means that certified operations must ensure
traceability of products transported by uncertified operations,
including if several uncertified transporters are used in sequence.
(Comment) Many comments discussed transloading organic agricultural
products and asked AMS to clarify if this activity requires
certification.
(Response) Transloading is commonly defined as the movement of
agricultural products between modes of transport. AMS does not have the
authority to regulate transport. Therefore, transloading strictly
between modes of transportation does not need to be certified.
However, transloading is sometimes used to describe the movement of
agricultural products from storage to transport or transport to
storage. AMS considers these activities to be loading and receiving
(see Sec. 205.2 and the definition of handle). Moving unpackaged
organic agricultural products from storage to transport, or from
transport to storage, requires certification. If the organic
agricultural products are enclosed in sealed, tamper-proof containers
or packages, then loading and receiving is exempt from certification.
Small Operations
(Comment) Several comments discussed the exemption for small
operations at Sec. 205.101(a). A few commenters asked AMS to clarify
if the exemption applies to both production and handling operations.
Others requested that AMS allow ingredients produced or processed by
such exempt operations to be used as certified organic ingredients
produced by other operations. One commenter requested AMS increase the
gross sales limit of $5,000.
(Response) This rulemaking does not modify current policy regarding
the exemption for small operations. Section 205.101(a) exempts
operations that produce or handle agricultural products as ``organic''
but whose gross agricultural income from organic sales totals $5,000 or
less annually. However, these operations must not sell, label, or
represent agricultural products they produce or process as certified
organic, and such products must not be used as certified organic
ingredients in products processed by another operation (see Sec.
205.310). Additionally, the $5,000 gross sales threshold is set by the
OFPA, and AMS does not have authority to increase this limit.
Selling and Representing
(Comment) Many comments requested that AMS provide exemptions for
operations that do not physically handle or contact organic
agricultural products, arguing that such operations do not threaten
organic integrity.
(Response) AMS disagrees with commenters' claim that lack of
physical contact equals low risk. Organic integrity depends on
oversight and transparency across the entire organic supply chain--
including some operations that may never physically contact organic
products. The need for certification is based on risk and this rule
requires certification of high-risk operations such as importers,
traders, and others that facilitate the sale of organic products.
Although these operations may not physically contact organic products,
they control critical events along organic supply chains where organic
integrity can be compromised, including purchase, sale, transport,
storage, and combining or splitting products. For example, an importer,
broker, or trader could unintentionally compromise the integrity of
organic products they buy or sell by not seeking or keeping records to
demonstrate traceability and verify organic integrity. Without these
records, there is no way to verify that a product was properly handled
by the multiple physical handlers in a supply chain. A breach of
integrity could go unreported, and the importer or trader would
unintentionally sell a product that has lost its organic status and
integrity. Similarly, brokers and traders could mistakenly direct
contracted storage facilities and transporters to perform activities
that compromise organic integrity, such as directing a storage facility
to fumigate a container of organic wheat or directing a transporter to
combine loads of organic and nonorganic corn.
Additionally, because importers, brokers, traders and others that
facilitate sales have direct financial interest in the transaction of
organic products, they have the incentive and opportunity to commit
fraud. For example, an operation could falsify records to claim that a
nonorganic product is certified organic, or direct a contracted storage
facility or transporter to mix organic and nonorganic products, and
then claim the entire load is organic. NOP has investigated many
notable cases of fraud committed by uncertified operations that did not
physically contact the products in question (see the discussion on
fraud under ``Purpose and Need for the Rule'').
The risk of both unintentional breach of integrity and fraud has
grown with the organic market as supply chains increase in complexity
and more uncertified parties affect control of organic products and
their transaction. Requiring certification based on risk ensures
traceability, verification, accountability, and oversight at the most
critical points of the supply chain, including the activities of
brokers, traders, importers, and others who facilitate sale but may not
physically contact organic products. The rule also provides reasonable
exemptions for low-risk operations to reduce cost and administrative
burden to the industry.
(Comment) Many comments discussed private labeling and brand
ownership of organic products. Opinions differed about the need to
certify these operations. Some commenters argued that requiring
certification of these operations would improve transparency and
traceability of products, while others claimed that doing so would be
unnecessary and create potential problems with labeling and
traceability.
(Response) ``Brand owners'' or operations that sell or distribute
organic products produced by another operation on their behalf may be
exempt from certification if they meet the criteria of Sec.
205.101(f). This exemption allows the buying, selling, receiving,
storing, and preparing for shipment of organic products that are
packaged for retail sale. The products must be sealed in tamper-evident
packaging ready for retail sale, and the operation must not open or
otherwise handle the retail packages. Private labeling operations that
process organic agricultural products must be certified.
(Comment) Commenters asked AMS to clarify if sales brokers need to
be certified, including businesses that buy or sell only packaged
organic products.
(Response) Operations that sell, trade, or facilitate sale or trade
of organic agricultural products on behalf of a seller or oneself must
be certified. However, AMS is providing an exemption for operations
that only buy, sell, receive, store, or prepare for shipment organic
products packaged for retail sale (Sec. 205.101(f)). The products must
be sealed in tamper-evident
[[Page 3563]]
packaging labeled for retail sale, and the operation must not open or
otherwise handle the retail packages. Sale of organic products not
packaged for retail sale (e.g., bulk; unpackaged; packaged for
nonretail sale; unsealed, non-tamper-evident packaging) must be
certified.
Supply Chain Logistics
(Comment) Many comments asked AMS to provide a specific exemption
for Customs brokers licensed by U.S. Customs and Border Protection,
arguing that these operations only facilitate entry of imports into the
United States, and that their activities do not present a risk to
organic integrity.
(Response) AMS agrees that the activities of Customs brokers do not
threaten organic integrity. Therefore, Sec. 205.101(g) exempts from
certification licensed Customs brokers that only conduct Customs
business per 19 CFR 111.1. This exemption is limited to Customs
business; other activities conducted by a Customs broker that fall
within the definition of handle--including selling, importing, or
trading organic agricultural products--may require certification.
(Comment) Several comments asked AMS to clarify if businesses that
facilitate the storage and transport of organic agricultural products,
such as logistics brokers and freight forwarders, require
certification.
(Response) Logistics brokers, freight forwarders, and other
businesses that facilitate storage and transport of agricultural
products may be exempt if they meet the criteria of Sec. Sec.
205.101(e) or (h). These exemptions only apply to operations that
conduct or facilitate specific shipping, storing, or transport
activities. This may include logistics brokers or freight forwarders
who do not take ownership or physical possession of organic products
and only provide a service by connecting a consigner (or consignee)
with a carrier who transports/stores the products. Additionally,
transport of organic agricultural products does not require
certification if the transport operation does not handle the products
(see definition of handle in Sec. 205.2). Other handling activities--
such as selling, importing, or trading--must be certified.
(Comment) Many commenters responded to AMS's request for comment
about ports of entry. Most commenters agreed that the activities of
ports--such as loading, storing, receiving, combining, and splitting--
must be certified if unpackaged products are being handled. Comments
stated that handling of unpackaged goods at ports should be certified
because ports conduct physical activities that can compromise organic
integrity. Ports unload, move, split, combine, and store both organic
and nonorganic products, increasing the risk of commingling organic and
nonorganic products, and the risk of contamination with substances not
allowed in organic handling. In contrast, several comments from trade
associations state that requiring certification of port activities may
cause delays, increase costs, and may have limited positive impacts on
organic integrity. Several comments asked AMS for more clarification
about the need for ports of entry to be certified.
(Response) Ports of entry must be certified if the activities they
conduct meet the definition of handle and do not clearly fit an
exemption at Sec. 205.101(a)-(h).
Recordkeeping and Verification
(Comment) Several comments noted that proposed Sec. 205.101 did
not clearly explain the requirements and recordkeeping practices each
exempt operation must follow. A few comments also asked AMS to increase
the recordkeeping requirement for exempt operations to five years to be
consistent with requirements for certified operations.
(Response) AMS has revised Sec. 205.101 to clarify the
requirements and recordkeeping practices that exempt operations must
follow. Specific references to individual requirements are removed from
each exemption, and the introductory paragraph explains universally
that all exempt operations must follow the applicable production,
handling, and labeling requirements of subparts C and D. The preamble
further explains with specific examples of requirements exempt
operations may have to follow.
AMS has also removed recordkeeping requirements from individual
exemptions and replaced them with a single, consistent recordkeeping
requirement that applies universally to most exempt operations. AMS
retained the requirements for exempt operations to maintain records for
at least three years because there was not a compelling reason for
increasing that timeframe without prior notice.
(Comment) AMS received several comments asking who is responsible
for verifying exempt operations' compliance with the organic
regulations.
(Response) Certified operations are responsible for verifying the
compliance of the certified organic products they receive, including
those received from exempt operations. Section 205.201(a)(3) requires a
certified operation's OSP to include monitoring practices and
procedures to verify suppliers (including exempt suppliers) and the
organic status of products they receive. AMS is not prescribing how
certified operations should verify suppliers and products; this
provides flexibility for operations to develop and implement practices
that best suit their business and the products they handle.
B. Imports to the United States
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
------------------------------------------------------------------------
Section Final regulatory text
------------------------------------------------------------------------
205.2..................................... Terms Defined.
Definitions for Organic
exporter and Organic
importer.
205.273................................... Imports to the United
States.
Entire section.
205.300................................... Use of the term,
``organic.''
Paragraph (c).
------------------------------------------------------------------------
Purpose, Scope, and Authority
AMS is amending the USDA organic regulations by adding a new
section (205.273) requiring the use of the National Organic Program
Import Certificate (``NOP Import Certificate''). The NOP Import
Certificate is a transaction certificate, or data set, that contains
detailed information about the quantity and origin of organic product
being imported into the United States. Any organic agricultural product
imported to the United States must be associated with a valid NOP
Import Certificate, generated by the certifying agent of the final
certified exporter sending the product to the United States.
[[Page 3564]]
The purpose of the NOP Import Certificate is to document the
organic status and quantity of imported organic products as they travel
from a certified organic exporter in a foreign country to a certified
organic importer in the United States. The NOP Import Certificate
ensures an auditable business transaction by documenting that the
products in the shipment are organic and may be sold, represented, and
distributed as organic within the United States.
The mandatory use of NOP Import Certificates is authorized by the
Organic Foods Production Act (OFPA), as amended by the ``2018 Farm
Bill''.\18\ The OFPA specifies what information an NOP Import
Certificate must include (7 U.S.C. 6502(13)) and also stipulates that
the NOP Import Certificate must ``be available as an electronic
record'' and captured in a tracking system maintained by the U.S.
Government (7 U.S.C. 6514(d)). The OFPA also provides the Secretary
with broad authority to establish appropriate and adequate enforcement
procedures and any other requirements that the Secretary may determine
to be necessary (7 U.S.C. 6506).
---------------------------------------------------------------------------
\18\ See sections 10104(b)(3) and 10104(c) of the Agriculture
Improvement Act of 2018, Public Law 115-334. Available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
---------------------------------------------------------------------------
The NOP Import Certificate must be presented to U.S. Customs and
Border Protection (CBP) through the CBP Automated Commercial
Environment (ACE). The use of this standardized electronic format will
ensure consistency in data for auditing, surveillance, and enforcement
purposes. The OFPA, as amended by the 2018 Farm Bill, states that AMS
must establish a system of tracking NOP Import Certificates, and that
AMS ``may integrate the system into any existing information tracking
systems for imports of agricultural products'' (7 U.S.C. 6514(d) and
6522(c)).\19\
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\19\ See section 10104(c) of the Agriculture Improvement Act of
2018, Public Law 115-334. Available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
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Because the OFPA enables AMS to access information available in ACE
(7 U.S.C. 6521(c)), AMS is using ACE to accept NOP Import Certificate
data.\20\ ACE is an automated and electronic system for processing
commercial trade data. It is the primary system through which the
global trade community files information about imports and exports so
that admissibility into the United States may be determined by
government agencies (including AMS) to ensure compliance.
---------------------------------------------------------------------------
\20\ See sections 10104(h) and (j) of the Agriculture
Improvement Act of 2018, Public Law115-334. Available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
---------------------------------------------------------------------------
The data to be entered into ACE include fields for the information
needed to meet the requirements of an NOP Import Certificate as defined
in the OFPA: origin; destination; the certifying agent issuing the NOP
Import Certificate; harmonized tariff code, when applicable; total
weight; and the organic standard the product was certified to (7 U.S.C.
6502(13)). For the purposes of uploading and tracking NOP Import
Certificates, the data must be available as an electronic format to
meet the requirements of the OFPA (7 U.S.C. 6514(d)(1)).
Both the OFPA and the USDA organic regulations require certified
operations to maintain and make available to the Secretary records that
concern the production, harvesting, and handling of agricultural
products that are or that are intended to be sold, labeled, or
represented as organic. This includes sufficient records to provide an
audit trail to determine the source, type and quantity, transfer of
ownership, and transportation of any agricultural product labeled as
organic. Likewise, both the OFPA and the USDA organic regulations
require certifying agents to maintain and make available to the
Secretary records concerning its activities.
This policy also aligns with international guidelines and norms
related to organic oversight. NOP considered international standards
established by the Codex Alimentarius Commission (Codex) \21\ and norms
published by the International Federation of Organic Agriculture
Movements (IFOAM).\22\ Both provide for and support the use of
transaction shipment certificates such as the NOP Import Certificate.
---------------------------------------------------------------------------
\21\ Section 7 of the Codex Guidelines for the Production,
Processing, Labelling and Marketing of Organically Produced Foods
recommends imported organic products to be marketed only where the
competent authority or designated body in the exporting country has
issued a certificate of inspection stating that the lot designated
in the certificate was obtained within an organic system of
production, preparation, marketing, and inspection.
\22\ IFOAM Norms define a transaction certificate as a
``document issued by a certification body or by the operator,
declaring that a specified lot or consignment of goods is
certified.''
---------------------------------------------------------------------------
Change From Current Policy
NOP Import Certificates are currently only used for organic
products imported from countries with which AMS has an equivalence
determination. The USDA has established equivalence determinations with
Canada, the European Union, Switzerland, Japan, South Korea, Taiwan,
and the United Kingdom. Organic imports from Canada are accompanied by
an organic certificate that includes an attestation statement that the
products comply with the terms of the United States-Canada Organic
Equivalency Arrangement. Organic imports from the European Union,
Switzerland, Japan, South Korea, Taiwan, and the United Kingdom are
accompanied by an NOP Import Certificate. The certifying agent of the
exporter evaluates the request for an NOP Import Certificate, and upon
verification of the organic shipment, completes and issues an NOP
Import Certificate. Form NOP 2110-1 is currently used for this purpose.
In the past, AMS has not required NOP Import Certificates for
organic exports from countries with which the United States does not
have an organic equivalence determination. The rulemaking changes this
to make the use of NOP Import Certificates mandatory, regardless of an
imported product's country of origin or if that country has an
equivalency determination with USDA. Specifically, this rulemaking
requires that all imported products intended to be sold, represented,
labeled, or marketed as organic in the United States must be declared
as organic to U.S. Customs and Border Protection (CBP), using an NOP
Import Certificate.
Alignment of Policy With U.S. Customs and Border Protection Policies
and Systems
The OFPA, as amended by the 2018 Farm Bill, requires the
establishment of an Organic Agricultural Product Imports Interagency
Working Group, consisting of members of both the USDA and CBP (see 7
U.S.C. 6521a).\23\ The mandatory use of NOP Import Certificates
supports the working group's goal to ensure the compliance of organic
agricultural products imported into the United States.
---------------------------------------------------------------------------
\23\ See section 10104(i) of the Agriculture Improvement Act of
2018, Public Law No: 115-334. Available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
---------------------------------------------------------------------------
Under this policy, AMS and CBP will collaborate to verify that
imported organic products are associated with NOP Import Certificates.
In April 2020, the electronic version of the NOP Import Certificate was
deployed in ACE as an optional filing step for organic imports. The use
of the electronic NOP Import Certificate will be mandatory once this
rule is fully implemented.
NOP Import Certificates will be required for any commodity imported
into the United States that is being
[[Page 3565]]
manifested, sold, marketed, or labeled organic. NOP Import Certificates
are required for organic commodities regardless of value or size and is
not applicable for any di Minimis exemptions under current CBP
regulations.
Generating the NOP Import Certificate
This section describes how the NOP Import Certificate data are
generated. NOP Import Certificates must be generated using the USDA's
Organic Integrity Database. By the time the rule is fully implemented,
both USDA-accredited certifying agents and organic certifying agents
accredited by countries with which USDA holds an organic trade
arrangement or agreement (equivalence determination or recognition
arrangement) will have access to the Organic Integrity Database to
generate NOP Import Certificates. Only the Organic Integrity Database
can be used to generate valid NOP Import Certificates, and only
accredited organic certifying agents (USDA or under an organic trade
arrangement or agreement) are authorized to use the Organic Integrity
Database.
Where does the data for the NOP Import Certificate come from?
The data for the NOP Import Certificate is generated in the Organic
Integrity Database by the certifying agent of the exporter. The
exporter is responsible for facilitating the trading, selling,
consigning, shipping, or exporting of organic product from a foreign
country to the United States. An organic exporter must be certified
organic by certifying agents accredited by the USDA or certifying
agents authorized by a trade arrangement or agreement. Organic
exporters may be the final physical handler of organic products within
a foreign country, or they may be the entities that facilitate, sell,
or arrange the sale of organic products shipped to the United States.
This exporter is responsible for verifying that the organic product
complies with organic standards. This includes, but is not limited to,
verifying that the import has not been exposed to a prohibited
substance, treated with a prohibited substance as a result of
fumigation or treated with ionizing radiation at any point in the
products' movements across country borders.
How does the certifying agent evaluate the request for an NOP Import
Certificate?
The certifying agent determines the format of the NOP Import
Certificate request from the certified operation, based on the data
required for the Organic Integrity Database to generate the NOP Import
Certificate. The request for an NOP Import Certificate must include all
information required by the organic exporter's certifying agent to
complete the NOP Import Certificate. The certifying agent is required
to confirm the authenticity of the organic products covered by the NOP
Import Certificate using control systems it designs for this purpose.
The certifying agent must have and implement a documented organic
control system for intaking and approving or rejecting the validity of
an NOP Import Certificate request.
The certifying agent is responsible for ensuring that the issued
NOP Import Certificate is only associated with an amount of product
that has been verified to be certified organic. The certifying agent
has the authority to determine whether it will issue an NOP Import
Certificate for a specific shipment, or for a specific timeframe (e.g.,
weekly, monthly, season) and amount or volume ceiling. This
determination is to be based on the capacity and control systems of
both the certifying agent and the certified operation. There is no
limit on the length of timeframe a certifying agent chooses. However,
the certifying agent must choose a timeframe that is appropriate to
their administrative capacity and documented control system and allows
them to verify the integrity of the specific type and volume of import.
Once the certifying agent verifies the authenticity of the organic
export, the certifying agent enters or uploads the information needed
into the Organic Integrity Database. Each NOP Import Certificate must
be associated with a certified organic operation listed in the
database, identified by a 10-digit code. The Organic Integrity Database
will generate a unique NOP Import Certificate that includes both the
10-digit identifier for the operation and a unique numerical identifier
for the NOP Import Certificate. The certifying agent will provide the
NOP Import Certificate, or data set with the NOP Import Certificate
number, back to the certified organic exporter requesting the NOP
Import Certificate. The certifying agent can cancel or void a NOP
Import Certificate in the Organic Integrity Database at any time.
Transmitting the NOP Import Certificate From Exporter to Importer
The certified organic exporter provides the NOP Import Certificate
to the U.S. importer, who provides it to the specific entity
responsible for entering import information into the ACE system. This
is typically an importer or designated Customs broker. The NOP Import
Certificate data can be sent either electronically or via paper. The
U.S. importer or Customs broker enters the NOP Import Certificate data
into ACE as part of its standard import filing process; this process is
governed by timelines determined by CBP. Organic certifying agents will
not have access to ACE; this activity is done by the importer or its
Customs broker, using the NOP Import Certificate data provided by the
certifying agent to the exporter.
As the certified organic product itself moves from the exporting
country into the United States, all entry documentation including, but
not limited to bills of lading, bills of sale, commercial invoices, and
packing lists must clearly state that the product is organic. Exporting
and importing operations must maintain records required under Sec.
205.103. CBP may hold shipments at the border to address health and
safety issues or violations of U.S. trade laws with a specific
commodity or shipment.
Importer Responsibilities
Upon receiving a shipment, an organic importer must verify that the
organic product(s) comply with the USDA organic regulations. This
includes ensuring that an NOP Import Certificate is associated with the
product received. It also includes verifying that the import has not
been treated with a prohibited substance as a result of fumigation or
treated with ionizing radiation at any point in the products' movements
across borders. Verification may take many forms, depending on the
documentation provided, and country and commodity. The importer must
have an organic control system that documents how this verification is
conducted to protect the organic integrity of imported product. This
control system is reviewed by the importer's certifying agent.
Both the organic exporter and U.S. organic importer must maintain
records of NOP Import Certificates, and these records must be available
for inspection by the NOP and certifying agents in accordance with
Sec. 205.103. Certifying agents that are overseeing imports of organic
products into the United States must have a system for ensuring that
operations receiving organic product are receiving and maintaining NOP
Import Certificates, and that they are not accepting more product from
any providers than is authorized by NOP Import Certificates.
[[Page 3566]]
Connecting NOP Import Certificate With ACE Import Data
Once NOP Import Certificate Data is entered into ACE, the data are
transmitted to AMS for analysis, surveillance, and enforcement. AMS
will align and validate the data generated in ACE with the original NOP
Import Certificate entered into the Organic Integrity Database. This
will connect the data about the actual imported product back to the
data about the corresponding authorized export, aligning both sides of
the transaction. This alignment will allow for the identification of
any anomalies or indicators of fraud, such as: NOP Import Certificates
in ACE that were not authorized (do not have a valid certificate
number) by a certifying agent in the Organic Integrity Database (e.g.,
fraudulent certificates); volumes of product entered in ACE that exceed
those authorized in the Organic Integrity Database; and/or entries into
ACE that are associated with an operation that is no longer certified.
This type of automated data-driven surveillance is a common approach in
trade oversight.
Timing of the NOP Import Certificate
The timing of the NOP Import Certificate data entry into ACE must
comply with current CBP import filing requirements for Partner
Government Agencies. The certified organic exporter must time the NOP
Import Certificate request in such a way that the certifying agent has
time to consider the request and generate the NOP Import Certificate,
and the exporter has time to deliver it to the importer or Customs
broker before the CBP filing requirements for the product.
Requiring an NOP Import Certificate provides trackable and
auditable verification that organic products comply with the USDA
organic regulations. This requirement will also support investigations
if noncompliant products are exported and misrepresented as organic for
sale in the United States. Given that the Organic Integrity Database
will be the definitive tool for generating NOP Import Certificates,
additional guidelines on data entry to generate NOP Import Certificates
will be provided through that system.
Summary of Changes to the Final Rule
AMS made several changes to the regulatory text of the SOE proposed
rule when writing this final rule. Changes to the final rule are
discussed below and are followed by responses to specific themes from
public comment.
AMS removed ``owner'' from the definition of organic
exporter, added ``certified'' before ``exporter,'' and ``to the United
States'' after ``from a foreign country.'' This clarifies that the
organic exporter must be certified, and that the organic exporter may
be the final physical handler of organic products within a foreign
country, or they may be the entities that facilitate, sell, or arrange
the sale of organic products shipped to the United States. This was
done to clarify questions about ``who needs to be certified'' received
during public comment.
AMS removed ``of record'' from the definition of organic
importer and added a statement that the organic importer is responsible
for entering NOP Import Certificate data into ACE. This addresses
public commenters' request to clarify the role of the organic importer
and the person responsible for entering data into ACE.
AMS removed ``through a U.S. Port of Entry,'' as all
imports must enter through such a Port, so the phrase is not needed.
AMS removed references to ``or equivalent data source''
and ``NOP Form 2110-1'' throughout Sec. 205.273 and clarified that the
Organic Integrity Database must be used to issue NOP Import
Certificates. AMS has determined that the Organic Integrity Database
will be the only data source for NOP Import Certificates because it is
a preexisting, proven tool that meets U.S. government security
requirements, and already accepts data in multiple different forms to
accommodate data inputs from other systems. The Organic Integrity
Database is already used and understood by certifying agents, including
many accredited by both the USDA and trade partner countries. It is a
system that accepts data in multiple forms, that any government can
engage with, and that minimizes onboarding time and learning curve.
Using the Organic Integrity Database as a single source of
certification and import data, while allowing multiple data upload
methods, will provide secure access to import data that facilitates the
use of NOP Import Certificates.
AMS clarified that certifying agents may issue NOP Import
Certificates for a specific timeframe, if appropriate, not limited to a
single transaction. This addresses public commenters' concerns about
generating NOP Import Certificates for multiple shipments in short
timeframes (e.g., multiple shipments of fresh produce across the
border). This change allows certifying agents to determine whether they
will issue an NOP Import Certificate for a specific shipment or for a
specific timeframe (e.g., weekly, monthly, seasonally) and amount or
volume ceiling. Because certifiers conduct certification activities on
a one-year cycle, it is expected that import certificates are unlikely
to exceed one year in duration. The certifying agent must choose a
timeframe that is appropriate to their administrative capacity and
documented control system, and allows them to verify the integrity of
the specific type and volume of import.
AMS clarified the requirement that certifying agents must
have and implement a documented organic control system for intaking and
approving or rejecting NOP Import Certificates. This ensures that
certifying agents have auditable processes and procedures that NOP can
audit to assess certifying agents' ability to generate and approve NOP
Import Certificates.
AMS removed the requirement that certifying agents must
issue NOP Import Certificates within 30 days. This avoids any timing
discrepancy between NOP Import Certificate data entry and CBP import
filing requirements. AMS does not have authority to change CBP entry
requirements. The timing of the NOP Import Certificate data entry into
ACE must comply with current CBP import filing requirements for Partner
Government Agencies.
AMS clarified that organic importers must have a
documented organic control system to verify NOP Import Certificates and
verify no contact with prohibited substances or exposure to ionizing
radiation. This is necessary to ensure that organic importers have
auditable processes and procedures that certifying agents can review to
assess importers' ability to verify NOP Import Certificates and verify
the integrity of imported organic products.
AMS clarified that organic importers must verify that the
NOP Import Certificate data accurately reflects the shipment, which may
include verification of quantities and types of product specified on
the NOP Import Certificate. This requirement more clearly states the
organic importer's responsibility in assessing and ensuring the
integrity of imported products, providing an additional layer of
oversight at a critical juncture in organic supply chains.
Summary of Public Comment
The majority of public comments were strongly in support of AMS's
proposed mandatory use of NOP Import Certificates. Many comments
discussed or recommended changes to the NOP Import Certificate process,
including the timing of NOP Import Certificates, ACE data entry, how
the certificate should travel with the import, certifying agent
[[Page 3567]]
role and capacity, and how the NOP Import Certificate would function
within organic trade arrangements and agreements.
Comments frequently asked AMS to clarify if NOP Import Certificates
can be issued before or after shipment. They also noted that the
proposed 30-day requirement to issue NOP Import Certificates does not
align with the 10-day ACE entry deadline noted in the preamble. Some
comments requested that AMS allow up to 30 days to enter NOP Import
Certificate data into ACE, while others recommended 10 days or less to
help reduce fraud.
Many comments asked AMS to clarify if an NOP Import Certificate
must ``accompany'' an import or be ``associated with'' an import.
Several comments requested that AMS require imports be ``accompanied''
by an NOP Import Certificate and that the certificate travel with the
import and be presented at entry into the United States, claiming that
this would help prevent fraudulent organic products from entering the
U.S. market. Others stated a preference to allow NOP Import
Certificates to ``be associated'' with shipments, noting that this
flexibility is needed to match the frequency and pace of land imports
via truck and rail.
Several comments noted that issuing NOP Import Certificates for
individual shipments would be difficult for high-volume, high-frequency
imports, especially those from Canada and Mexico. These comments asked
AMS to consider allowing certifying agents to issue NOP Import
Certificates that cover a specific time period (e.g., quarterly),
product type, and volume. Comments argued this would reduce
administrative burden and cost to both certified operations and
certifying agents. A few comments also claimed that some certifying
agents may not have the administrative capacity or technical expertise
to issue and verify NOP Import Certificates as proposed.
A few comments asked AMS to clarify the definitions and roles of
exporters and importers, noting that it is not clear who is responsible
for requesting NOP Import Certificates, verifying them upon import, and
entering data into ACE. Some comments also asked AMS to further define
``equivalent data.''
Finally, some comments requested clarification about the general
applicability and use of NOP Import Certificates, including their use
for very small or infrequent shipments, use by exporters in a country
AMS has a trade arrangement or agreement with, use of electronic vs.
paper certificates, and use in trade between two foreign countries.
Responses to Public Comment
Timing of NOP Import Certificates
(Comment) AMS received many comments concerning the 30-day time
frame for certifying agents to review and issue NOP Import
Certificates. Commenters stated that the 30-day timeframe will
negatively impact imports of perishable organic product from Canada and
Mexico that require a rapid import process.
Other commenters stated that the 30-calendar-day timeframe for
certifying agents to review and issue NOP Import Certificates does not
align with the existing 10-day requirement to upload the NOP Import
Certificate data into the ACE system. Others requested that the 10-day
requirement for organic exporters to enter data from an NOP Import
Certificates or equivalent into ACE align with the proposed 30-day
requirement for certifying agents to issue an NOP Import Certificate or
equivalent. Commenters also requested that the 10-day timeframe to
enter NOP Import Certificate data be reduced to prevent organic fraud.
More broadly, AMS received comments asking if NOP Import
Certificates can be issued both before and after shipment.
Additionally, commenters asked If NOP Import Certificates could be
issued after the shipment of organic product has already entered the
United States.
(Response) The timing of the NOP Import Certificate data entry into
ACE must comply with current CBP import filing requirements for Partner
Government Agencies. AMS does not have authority to change CBP entry
requirements.
The certified organic exporter must time the NOP Import Certificate
request in such a way that the certifying agent has time to consider
the request and generate the NOP Import Certificate, and the exporter
has time to deliver it to the importer or Customs broker before the CBP
filing requirements for the product.
To address the problem of generating NOP Import Certificates for
multiple shipments in short timeframes (e.g., multiple shipments of
fresh produce across the border), AMS is granting the certifying agent
the authority to determine whether it will issue an NOP Import
Certificate for a specific shipment, or for a specific timeframe (e.g.,
weekly, monthly, season) and amount or volume ceiling. The certifying
agent is responsible for ensuring that the issued NOP Import
Certificate is only associated with an amount of product that has been
verified to be certified organic.
Associated vs. Accompanying
(Comment) Several commenters noted that proposed Sec. 205.273(d)
states that the organic importer of record must ensure that the
shipment is accompanied by a verified NOP Import Certificate. This
conflicts with the preamble which states that shipments of organic
product must be associated with a valid NOP Import Certificate.
(Response) To clarify the requirement, AMS has removed the term
accompanied from the rule. The NOP Import Certificate must be
associated with a shipment. This revision accurately describes AMS's
intent that organic shipments are associated with, and not accompanied
by, a valid NOP Import Certificate at the time of entry into the United
States.
(Comment) Commenters requested that the term associated, located in
the preamble text, be changed to accompany and that AMS require NOP
Import Certificates to be available upon entry to the United States, to
prevent fraud in the organic market.
(Response) USDA is requiring that all organic exports to the United
States be associated with a valid NOP Import Certificate. By requiring
organic imports to be associated with, and not accompanied by, an NOP
Import Certificate, USDA will have access to the import data without
restricting or slowing import and trade of organic products.
Certifying Agent Capacity
(Comment) AMS received several comments highlighting that organic
certifying agents lack the capacity to issue the number of NOP Import
Certificates that would be required under the proposed rule at one per
shipment. Comments specifically referenced the high-volume of organic
products coming by truck and rail from Mexico and Canada.
(Response) It is the certifying agent's responsibility to ensure
that the exporting operation has the capacity to produce or handle the
product covered by the NOP Import Certificate. When a certifying agent
issues a NOP Import Certificate, it is validating that the product is
truly organic; therefore, it must have adequate control systems to
verify these claims.
To address the problem of generating NOP Import Certificates for
multiple shipments in short timeframes (e.g., multiple shipments of
fresh produce across the border), AMS is granting the certifying agent
the authority to determine whether it will issue an NOP Import
Certificate for a specific shipment, or for a specific timeframe
[[Page 3568]]
(e.g., weekly, monthly, season) and amount or volume ceiling. The
certifying agent is responsible for ensuring that the issued NOP Import
Certificate is only associated with an amount of product that has been
verified to be certified organic.
(Comment) AMS received several comments that recommended a
staggered implementation timeline for the NOP Import Certificate
requirement to ensure certifying agents have the administrative
capacity to process additional NOP Import Certificates. Several
comments also expressed concern about the increased cost associated
with issuing NOP Import Certificates. Comments noted that certifying
agents would need to hire and train additional technical staff to
comply with the proposed requirements for NOP Import Certificates.
(Response) Under the current USDA organic regulations, certifying
agents are not allowed to provide certification services that are
outside its administrative capacity. While a reasonable implementation
period is being provided to fully update the Organic Integrity Database
to generate NOP Import Certificates, certifying agents are not to issue
any NOP Import Certificates without having adequate expertise and
staffing to verify the organic status of products it oversees under the
organic program.
(Comment) Commenters asked how certifying agents will verify
whether a shipment is compliant with the USDA organic regulations based
on an NOP Import Certificate.
(Response) Certifying agents that are overseeing exports of organic
products to the United States must have and implement a documented
organic control system for intaking and then approving or rejecting an
NOP Import Certificate request. The certifying agent is responsible for
ensuring that the issued NOP Import Certificate is only associated with
an amount of product that has been verified to be certified organic.
Certifying agents that are overseeing importers of organic products
into the United States must have a system for ensuring that operations
receiving organic product are receiving and maintaining NOP Import
Certificates, ensuring that importers have met the requirements of this
section, and that they are not accepting more product from any
providers than is authorized by NOP Import Certificates.
General Applicability
(Comment) AMS received comments asking if NOP Import Certificates
would be required for small, retail, and mixed shipments of organic
product imported into the United States.
(Response) NOP import Certificates will be required for any
commodity imported into the United States that is being manifested,
sold, marketed, or labeled organic. NOP Import Certificates are
required for organic commodities regardless of value or size and is not
applicable for any de minimis exemptions under current CBP regulations.
A very limited number of exemptions will be allowed for items such as,
but not limited to, food donations, non-retail samples, and
humanitarian efforts.
(Comment) Commenters asked if NOP Form 2110-1, NOP Import
Certificate, is mandatory and whether a paper copy would be permitted.
Commenters also asked if certifying agents would issue physical or
digital copies of NOP-2110-1 to operations.
(Response) Only the NOP Import Certificate and its associated data,
generated from the Organic Integrity Database, is a valid NOP Import
Certificate. Either a paper-based or electronic NOP Import Certificate
may be used. Certifying agents will determine the format it will use to
provide the exporter with the NOP Import Certificate data.
ACE Data Entry
(Comment) We received comments requesting AMS clarify the
definition of ``equivalent data source'' by providing additional text
in Sec. 205.273(e). Commenters requested the requirement explicitly
state that USDA is the sole authority that determines equivalent data
sources.
(Response) In the final rule, we have removed the term ``equivalent
data source.'' All NOP Import Certificates will be generated using the
Organic Integrity Database. AMS provides multiple ways to upload or
enter data into the Organic Integrity Database. We have determined it
will be the only data source for NOP Import Certificates because it is
a preexisting, proven tool that meets U.S. government security
requirements, and a centralized system is needed to facilitate supply
chain traceability and to assess authorized import certificate data
against actual import data generated by CBP and reported back to AMS.
The Organic Integrity Database allows data submittals in multiple
formats, such as direct data entry, data spreadsheet uploads, and
automated programming interfaces. A data dictionary is also public,
allowing external parties to easily map their own systems and data
exports to the tool. The Organic Integrity Database is already used and
understood by certifying agents, including many accredited by both the
USDA and trade partner countries. It is a system that any government
can engage with that minimizes onboarding time and learning curve.
Using the Organic Integrity Database as a single source of
certification and import data, while allowing multiple data upload
methods, will provide secure access to import data that facilitates the
use of NOP Import Certificates.
(Comment) We received a number of comments about the respective
roles of the exporter and importer with respect to the NOP Import
Certificate. Several comments stated that the organic exporter does not
have access to the CBP ACE system and is not the party that would enter
the required data into ACE. Commenters recommended that the importer of
record be the entity responsible for entering data into ACE. Comments
stated that the proposed definition of organic importer of record is
unclear and does not reliably identify the party capable of ensuring
each shipment is associated with an NOP Import Certificate.
(Response) NOP Import Certificates must be generated by the
certified organic exporter's certifying agent, using the USDA's Organic
Integrity Database. Only the Organic Integrity Database can be used to
generate valid NOP Import Certificates, and only accredited organic
certifying agents (USDA or under an organic trade arrangement or
agreement) are authorized to use the Organic Integrity Database.
Once the NOP Import Certificate is generated in the Organic
Integrity Database, the exporter's certifying agent provides the NOP
Import Certificate, or data set with the NOP Import Certificate number,
back to the certified organic exporter who requested the NOP Import
Certificate. The certified organic exporter then provides the NOP
Import Certificate to the U.S. importer or buyer, who provides it to
the specific entity responsible for entering import information into
the ACE system. This is typically an importer or designated Customs
broker. That importer or Customs broker enters the NOP Import
Certificate data into the ACE system as part of its standard import
filing processes, including the Entry Summary Process. Organic
certifying agents will not have access to ACE; this activity is done by
the importer or its Customs broker, using the NOP Import Certificate
data provided by the certifying agent to the exporter.
(Comment) Commenters asked how imported organic product would be
identified in ACE without an organic
[[Page 3569]]
Harmonized Tariff Schedule (HTS) code.
(Response) The NOP Import Certificate in ACE has been programmed to
enable NOP Import Certificate entry for a wide range of products,
including agricultural products and textiles, not just those with an
organic HTS code. An organic HTS code is not required to upload NOP
Import Certificate data into ACE.
Trade Arrangements and Agreements
(Comment) AMS received comments requesting that foreign-based
certifying agents operating under recognition arrangements be required
to list organic operations in the Organic Integrity Database. As noted
by commenters, the absence of that data makes it difficult for
organizations to verify the certification status of foreign-certified
operations.
(Response) AMS is changing access to the Organic Integrity Database
to include organic certifying agents and operations operating under
organic trade arrangements or agreements, such as equivalency and
recognition arrangements. Certified organic operations covered under
trade arrangements or agreements will need to be listed in the Organic
Integrity Database by their certifying agents for the certifying agents
to be able to generate NOP Import Certificate for valid products
entering the United States as organic.
(Comment) We received comments asking how NOP Import Certificates
would apply to trade of organic products under, and outside of, an
equivalency arrangement. Additionally, commenters requested more
information about how NOP Import Certificates would apply to NOP-
certified products traded between foreign countries.
(Response) The NOP Organic Import Certificate is required for any
product imported into the United States that is being manifested, sold,
marketed, or labeled organic, regardless of the product's country of
origin or if that country has an equivalency determination with USDA.
Organic products imported from any country with which AMS has an
equivalency determination must follow the same NOP Import Certificate
requirements outlined in this rule. Other countries may also have their
own unique filing requirements for organic products coming into their
countries; organic businesses need to consult with their supply chains
to determine those requirements.
C. Labeling of Nonretail Containers
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.307............................................. Labeling of nonretail containers.
Paragraphs (a) through (c).
----------------------------------------------------------------------------------------------------------------
Accurate labeling of non-retail containers used to ship or store
organic products is critical to organic integrity. Proper labeling
reduces misidentification and mishandling, facilitates traceability and
product verification, reduces the potential for organic fraud, and
allows accurate identification of organic product by customs officials
and transportation agents.
Therefore, this rulemaking requires that all nonretail container
labels must identify contents as organic and include information
linking the container to audit trail documentation. Additionally, audit
trail documentation associated with a nonretail container must identify
the last certified operation that handled the product. Affected
entities may include but are not limited to: certified and noncertified
operations that store and transport organic product in nonretail
containers; certifying agents; and inspectors.
Background
The organic regulations previously only required a production lot
number on nonretail containers labels used to ship or store organic
product. Other information--such as identification of the product as
organic, and special handling instructions--were optional, but not
required on nonretail container labels. Based on the NOP's experience
enforcing the organic regulations, this lack of information created
gaps in the organic chain of custody, complicated the verification of
organic integrity, and increased the likelihood of organic fraud.
To reduce the prevalence of organic fraud and increase oversight of
organic supply chains, nonretail containers are now required to be
marked with a statement identifying the product as organic and must
include unique information that will link the nonretail containers to
audit trail documentation. Unique identifying information could include
lot numbers, shipping information, or a unique identifier for that
shipment. Accurate labeling will identify contents as organic as a
container moves through the supply chain; this will reduce mishandling
and help maintain an audit trail and improve traceability.
Nonretail Containers: Description and Use
Nonretail containers are defined under Sec. 205.2 of the USDA
organic regulations as ``any container used for shipping or storage of
an agricultural product that is not used in the retail display or sale
of the product.'' Nonretail containers are used to ship or store either
packaged or unpackaged organic products, and may include the following:
Produce boxes, totes, bulk containers, bulk bags, flexible
bulk containers, harvest crates and bins;
Boxes, crates, cartons, and master cases of wholesale
packaged products; and
Trailers, tanks, railcars, shipping containers, vessels,
cargo holds, freighters, barges, grain elevators, silos, grain bins, or
other methods of bulk transport or storage.
Nonretail containers are not used to display organic products for
sale to the consumer at retail establishments. Packages that display
organic products for retail sale to the consumer must be labeled
according to Sec. Sec. 205.303 and 205.306.
What must be included on nonretail container labels?
Nonretail containers used to ship or store organic products must be
clearly labeled with a statement that identifies the product as
organic. Clearly visible organic identification alerts handlers that
the contents of the nonretail container may require special care, thus
reducing accidental mishandling of the product, such as treatment with
a prohibited substance or commingling with conventional product during
transport and storage. Operations may use abbreviations or acronyms to
identify products as organic, provided that they are clear and easily
understood. This provides flexibility for
[[Page 3570]]
operations to meet the requirements of Sec. 205.307(a)(1) and makes it
easier to label containers with limited space or containers that are
difficult to label due to their size, shape, material, or use.
Nonretail containers must also be clearly labeled with information
that links the container to audit trail documentation (see Sec. 205.2
for definition of audit trail). This could be a production lot number,
shipping identification, or other unique information that handlers can
use to trace the container to its associated audit trail documentation.
This creates a clear link between container and audit trail and
minimizes the size of labels by allowing some information to be listed
in associated documentation, instead of directly on the nonretail
container label.
Operations may use temporary labels or signage to meet the
requirements of Sec. 205.307(a). This provides additional flexibility
for containers that may be difficult to label due to size, shape,
material, or use.
Revisions to Sec. 205.307 do not limit the information that can be
on a nonretail label. This gives operations the flexibility to include
details they deem critical to the integrity of specific products. For
example, an operation may opt to include special handling instructions,
the USDA organic seal for qualifying products, the operation or
certifying agent name, or contact information on the nonretail label.
Nonretail Containers and Audit Trail Documentation
Nonretail containers used to ship or store organic products must be
labeled with information that links the container to audit trail
documentation (Sec. 205.307(a)(2)). Such documentation must be
sufficient to determine the source, transfer of ownership, and
transportation of the product (see definition of audit trail in Sec.
205.2) and must identify the last certified operation that handled the
product (Sec. 205.307(b)).
Listing the last certified organic operation provides a point of
contact to verify the organic status of a product and supports
operations' traceability, recordkeeping, and fraud prevention
requirements (Sec. Sec. 205.103(b)(2)-(3) and 205.201(a)(3)). It also
supports on-site inspections and supply chain traceability audits
conducted by certifying agents (Sec. Sec. 205.403(d)(5) and
205.501(a)(21)) by ensuring good recordkeeping of the critical
transfers between certified operations.
Exception to Organic Identification on Nonretail Containers
Nonretail containers used to ship or store agricultural products
packaged for retail sale with organic identification visible on the
retail label are not required to identify product as organic per Sec.
205.307(a)(1). Examples include master cases and pallets where the
organic identification (e.g., the USDA organic seal) of individual
retail units is visible. These are exempt from Sec. 205.307(a)(1)
because the organic identification is visible on the retail label.
These types of nonretail containers are only excepted from the
requirements of Sec. 205.307(a)(1). All nonretail containers must be
linked or traceable to audit trail documentation per Sec.
205.307(a)(2); this ensures traceability of the product in the
containers and supports organic integrity during transport, storage,
and handling.
Summary of Changes to the Final Rule
AMS made several changes to the regulatory text of the SOE proposed
rule when writing this final rule. Changes to the proposed rule are
discussed below and are followed by specific themes from public
comment.
AMS simplified the requirement to list full organic
identification (e.g., ``100 percent organic,'' or ``made with organic .
. .'') to ``identification of product as organic,'' which provides more
flexibility to operations and shortens the organic identification
statement without changing the statement's intent or its utility as
immediate and clear identification of nonretail containers. This change
was made in response to public comment.
AMS revised the requirement to list production lot numbers
or shipping identification. This information is now used to link a
container to audit trail documentation. To reduce administrative burden
and cost to operations, AMS is only requiring the most critical
information on nonretail container labels: organic identification and
information that links the container to audit trail documentation. This
maintains traceability and integrity by requiring nonretail containers
to be linked to audit trail documentation, which must identify the last
certified operation that handled the product and must be sufficient to
determine the source, transfer of ownership, and transportation of the
product.
AMS removed the requirement to identify the product's
certifying agent on nonretail labels because this information may be
included in audit trail documentation linked to nonretail containers.
Removing this requirement limits information on nonretail labels to the
most critical information, thereby reducing cost and burden without
sacrificing integrity.
AMS added a requirement that audit trail documentation
associated with a nonretail container must identify the last certified
operation that handled the product. This allows operations to verify
the source of organic products they receive and provides a record trail
that certifying agents can use to conduct full supply chain
traceability audits and verify organic status.
The final rule no longer requires organic identification
on nonretail containers of retail-labeled products. This avoids undue
administrative burden, cost, and redundant information when organic
identification is already visible on the products' retail labels.
AMS removed the list of optional information that may be
listed on nonretail container labels. This list is not necessary
because operations may optionally include any additional information on
nonretail labels if they wish.
Summary of Public Comment
Public comments strongly supported mandatory organic identification
on nonretail container labels. However, many comments requested the
flexibility to use alternatives like abbreviations and common names.
Commenters stated that the proposed rule's requirement to use specific
(and sometimes lengthy) statements would add cost and be difficult to
apply to containers with limited space. Commenters also requested that
AMS require generic product names--e.g., ``organic tomatoes''--on
labels, claiming that this information is needed to quickly identify
the contents of nonretail containers.
Other commenters requested AMS mandate additional information on
large nonretail container labels to include country of origin, special
handling instructions, and the USDA organic seal. Additionally,
comments pointed out that nonretail labels should not be limited to the
information explicitly listed in Sec. 205.307, and requested that NOP
allow operations to include other types of information on labels.
Responses to Public Comment
(Comment) We received comments requesting AMS require all nonretail
containers display the information described in Sec. 205.307,
regardless of size or type (i.e., not allow exceptions for large
nonretail containers used for transport or storage). Additionally,
commenters noted that there was no definition or description outlining
what type of containers would be exempt from the labeling requirements.
[[Page 3571]]
(Response) All nonretail containers of organic products must be
labeled with information that links the container to audit trail
documentation, regardless of size, shape, or use. This ensures
information needed to verify and trace the product is available to
those handling the product. Only nonretail containers used to ship or
store agricultural products packaged for retail sale with organic
identification visible on the retail label are excepted from the
requirements of Sec. 205.307(a)(1).
(Comment) Commenters requested the name and contact information of
the certified operation be a mandatory field on all nonretail container
labels because a certifying agent name alone is not sufficient to match
a physical product to an organic certificate. Other commenters also
requested that the operation's address or the NOP operation ID also be
included.
(Response) AMS is only requiring the most critical information on
nonretail container labels: organic identification and information that
links the container to audit trail documentation. This reduces
administrative burden and cost to operations. Traceability and
integrity are maintained by requiring nonretail containers be linked to
audit trail documentation, which must identify the last certified
operation that handled the product. Audit trail documentation must be
sufficient to determine the source, transfer of ownership, and
transportation of the product (see audit trail in Sec. 205.2).
(Comment) We received comments requesting that listing the
certifying agent be optional because it was redundant for master cases
of retail-packaged product and added to the cost of the label.
(Response) AMS does not require listing the certifying agent on
nonretail container labels. Such information may be listed in audit
trail documentation; operations may choose to do this to verify organic
status of the product or determine the source, transfer of ownership,
and transportation of the product. Section 205.307(c) excepts nonretail
containers of retail-packaged products from listing organic
identification if the retail packages clearly identify the product as
organic.
(Comment) AMS received comments noting both disagreement and
confusion regarding which operation/certifying agent pair is required
to be on the nonretail label. Commenters stated that the proposed
revision (``producer of the product, or . . . the last handler that
processed the product'') may not indicate the appropriate operation for
verification purposes or in private labeling scenarios.
(Response) Section 205.307(b) requires that a nonretail container's
audit trail documentation identify the last certified operation that
handled the product. The certifying agent that certified this handler
may be listed in audit trail documentation; operations may choose to do
this to verify organic status of the product or determine the source,
transfer of ownership, and transportation of the product.
(Comment) We received comments stating that special handling
instructions are critical to the integrity of organic products in the
supply chain and requested that AMS make this information mandatory on
all labels. Commenters also inquired about what special handling
instructions should include.
(Response) We are not requiring special handling instructions on
nonretail container labels; this reduces administrative burden and cost
to operations without risking integrity. Operations may include special
handling instructions (or other information) on nonretail containers if
they deem it necessary.
(Comment) AMS received comments requesting the mandatory use of
tamper-evident seals on nonretail containers. Commenters argue that
tamper-evident seals may help prevent fraud and mishandling of organic
product.
(Response) AMS is not requiring tamper-evident seals on nonretail
containers; this avoids potential undue administrative burden and costs
to operations. Operations may use tamper-evident seals on nonretail
containers if they deem it necessary.
D. On-Site Inspections
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definition for Unannounced inspection.
205.403............................................. On-site inspections.
Paragraphs (b)(1) and (2) and (d)(4) and (5).
----------------------------------------------------------------------------------------------------------------
On-site inspections of certified organic operations are a
critically important tool used to verify an operation's compliance with
the Act and the organic regulations. This rulemaking strengthens the
utility of on-site inspections by requiring that certifying agents:
Conduct a minimum number of unannounced inspections each
year.
Conduct mass-balance audits during on-site inspections.
Verify traceability of product and ingredients within an
operation during on-site inspections.
Verify traceability of product in an operation's supply
chain back to the last certified operation during on-site inspections.
These requirements will strengthen organic integrity and supply
chain traceability by requiring the use of proven best practices during
inspection of organic production and handling. Entities affected by
this policy may include certifying agents, certified operations, and
operations applying for certification. Organic stakeholders should
carefully examine the regulatory text and policy discussion below.
Unannounced Inspections--Background
Unannounced inspections are an effective and useful tool to ensure
compliance across certified operations and bolster consumer trust in
the organic label. NOP previously issued an instruction (NOP
Instruction 2609) on unannounced inspections, which recommends that
certifying agents conduct unannounced inspections of five percent of
their total certified operations per year as a tool for ensuring
compliance with the regulations.\24\ This NOP instruction was supported
by a recommendation made by the NOSB in December 2011.\25\ The organic
regulations previously allowed for, but did not require, unannounced
inspections, leaving this to the discretion of the certifying agent.
[[Page 3572]]
Therefore, AMS has codified the requirement for certifying agents to
conduct a minimum number of unannounced inspections annually of
certified operations.
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\24\ NOP 2609, Instruction, Unannounced Inspections. September
12, 2012. Available in the NOP Program Handbook: https://www.ams.usda.gov/sites/default/files/media/2609.pdf.
\25\ NOSB Recommendation, Unannounced Inspections. December 2,
2011. Available on the AMS website: https://www.ams.usda.gov/sites/default/files/media/NOP%20CACC%20Final%20Rec%20on%20Unannounced%20Inspections.pdf.
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Use of Unannounced Inspections
To clarify the difference between unannounced inspections and full
annual inspections, AMS is defining the term unannounced inspection as
``The act of examining and evaluating all or a portion of the
production or handling activities of a certified operation without
advance notice to determine compliance with the Act and the regulations
in this part.'' \26\ Note that unannounced inspections are different
from a full annual inspection because the scope of the inspection may
be limited to a portion of the operation or the operation's activities,
and certifying agents must conduct the inspection without advance
notice.
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\26\ Compare to the definition of inspection at 7 CFR 205.2: The
act of examining and evaluating the production or handling operation
of an applicant for certification or certified operation to
determine compliance with the Act and the regulations in this part.
---------------------------------------------------------------------------
Scope of Unannounced Inspections
Relative to a full annual on-site inspection, an unannounced
inspection may be limited in scope, depth, and breadth and may cover
only a portion of the operation or the operation's activities, such as
parcels, facilities, products, or a review of records. This allows
unannounced inspections to be used as a risk-based tool to address
specific needs, such as investigation of a complaint or high-risk area.
Inspectors may conduct sampling during an unannounced inspection.
Samples collected may count towards the number of samples a certifying
agent must collect annually per Sec. 205.670(d) of the organic
regulations. Sample collection alone, however, does not qualify as an
unannounced inspection.
When unannounced inspections are limited in scope, they are not
required to follow the requirements of Sec. 205.403(c)(2), (d), or
(e). This means unannounced inspections:
May be conducted when an authorized representative of the
operation is not present and the inspector is not trespassing.
May be conducted at any time of year.
Do not have to verify all areas or activities of the
operation like a full, annual inspection.
Do not have to include an exit interview with an
authorized representative of the operation.
An unannounced inspection may fulfill the requirement for a full
annual on-site inspection, provided that the inspector meets all
requirements for an annual on-site inspection per Sec. 205.403. This
includes meeting the timing, scope, exit interview and documentation
requirements for annual inspections. The exception is that the
inspection would not be scheduled in advance with the operation's
awareness. If an unannounced inspection will serve as the annual
inspection, an authorized representative must be present.
Selecting Operations for Unannounced Inspections
To maximize the effectiveness of unannounced inspections,
certifying agents are encouraged to select operations from a range of
different production and handling types, products, and locations.
Operations may be selected randomly, by risk, in response to a
complaint or investigation, or other criteria. The number of
unannounced inspections to be conducted annually should be calculated
by rounding up to the nearest whole number, so that certifying agents
with very few certified operations (e.g., under 20 operations) are
still required to conduct at least one unannounced inspection per year.
Planning and Scheduling Unannounced Inspections
Unannounced inspections should be conducted without advance notice
to the operation. However, some unannounced inspections may require
advance notice (e.g., to ensure that portions of an operation are
accessible or safe to access). Therefore, a certifying agent may notify
an operation up to four hours prior to the inspector arriving onsite.
As a best practice, certifying agents are encouraged to disclose their
process for unannounced inspections, including a policy on inspector
access to certified operations, and to train inspectors to prevent
trespassing or breaking laws when accessing an operation. An
operation's refusal to allow an inspector access to any portion of the
operation is a violation of Sec. 205.403 and warrants a notification
of noncompliance.
Following an unannounced inspection, an inspection report must be
written by the inspector and reviewed by the certifying agent. The
results of the inspection must be communicated to the inspected
operation per Sec. 205.403(f) and the certifying agent's internal
protocols.
Certifying Agent Ability To Conduct Unannounced Inspections
Certifying agents must be able to conduct unannounced inspections
of any operation they certify. Therefore, AMS requires that certifying
agents only accept applications for certification or continue
certification from operations for which the certifying agent is able to
conduct unannounced inspections. To ensure consistency, transparency,
and accountability, certifying agents are expected to describe the
areas where they operate in the written materials they provide to both
applicants and certified operations, and review the locations of all
operations during their application review or annual review.
A certifying agent that cannot conduct unannounced inspections in
an applicant's or certified operation's location due to logistical
challenges, staffing, security, or other reasons, is considered to not
have the administrative capacity for certification activities in that
area, consistent with Sec. 205.501(a)(19). In this case, the
certifying agent must document the specific reasons it does not have
the administrative capacity to certify in that area, and must inform
the applicant or certified operation to seek certification from another
certifying agent. If new certification is not obtained, the operation's
certification would be suspended/revoked. This process is similar to
the current procedures used when a certifying agent surrenders its
accreditation or is suspended/revoked.
For additional information about unannounced inspections,
certifying agents may refer to NOP Instruction 2609.
Mass-Balance and Traceability Audits During On-Site Inspections
Traceability of organic products is critical to verification of
organic integrity. Therefore, AMS requires that certifying agents
verify quantities and traceability of organic products produced or
handled by an operation through mass-balance and traceability audits.
Audit tools are the premier methods to verify organic integrity. The
importance of audits has increased because transaction certificates,
which certifying agents relied upon in the past to verify the organic
status of specific loads or sales or organic products, are neither
required by the USDA organic regulations nor universally issued by
certifying agents.
Mass-Balance Audits
During on-site inspections, certifying agents must verify that the
quantities of organic product and ingredients
[[Page 3573]]
produced or purchased by an operation accounts for organic products and
ingredients used, stored, sold, or transported by the operation (Sec.
205.403(d)(4)). Commonly known as a ``mass-balance'' or ``in-out''
audit, this verification is an effective method of detecting and
discouraging organic fraud.
Mass-balances may be performed on products that are produced on an
operation, but then used or stored on-site and not sold (e.g., silage
produced on-site as feed for dairy animals). Mass-balance covers
quantities of agricultural products; other quantitative assessments
such as dry matter intake and stocking rate verification are not mass-
balances. To conduct these mass-balance audits, certifying agents may
choose a sub-set of products based on risk or other factors. With
respect to multi-ingredient products, certifying agents may choose a
single ingredient or multiple ingredients to mass-balance. When a
single ingredient is selected, a best practice is to choose an
ingredient that is high-risk or used in several products.
Mass-balances do not replace the recommended best practice of also
conducting yield analyses at producer operations. Yield analysis looks
at whether harvested quantities are consistent with expected yields.
This is an important tool to assess the potential for commingling of
noncertified/nonorganic products with organic products.
Traceability Audits
Successful traceability within organic supply chains requires three
basic elements: (1) traceability within a single operation; (2)
traceability one step back from an operation in a supply chain; and (3)
traceability by a third party along an entire supply chain, source to
consumer.
Therefore, during all annual inspections certifying agents must
verify the traceability of organic product both within an operation and
verify traceability back to an operation's suppliers (Sec.
205.403(d)(5)).\27\ This means that a certifying agent must verify that
an operation can trace the products it produces or handles during the
full time the operation possesses those products, from time of purchase
or acquisition, through production, to sale or transport. This includes
ingredients or products that the operation handles but may not own.
---------------------------------------------------------------------------
\27\ The third traceability element, traceability along an
entire supply chain, is addressed in 7 CFR 205.501(a)(21), and
discussed in this rulemaking in Section P, Supply Chain Traceability
and Organic Fraud Prevention.
---------------------------------------------------------------------------
Additionally, certifying agents must verify the traceability of
products from an operation's suppliers (Sec. 205.403(d)(5)). Because
supply chains sometimes include operations that are not certified,
certifying agents must verify compliance of organic products back to
the last USDA-certified organic operation. Certifying agents may verify
compliance back to the last certified operation by inspecting and
verifying audit trail documentation and other records kept by the
certified operation being inspected. This will ensure oversight of the
critical linkages between certified operations and support full
traceability and verification of organic products across supply chains.
Certifying agents must also conduct supply traceability chain
audits when circumstances meet criteria defined by the certifying agent
(Sec. Sec. 205.501(a)(21) and 205.504(b)(7)). These audits would not
be performed at every annual inspection.
Responses to Public Comment
Virtual/Remote Inspections
(Comment) Several public comments noted that during the COVID-19
pandemic, virtual inspections, or sometimes a hybrid of virtual an on-
site inspection, were temporarily used by certifying agents. Several
comments asked if AMS intends to allow the use of virtual inspections
for operations that have a demonstrated history of compliance or are at
low risk of organic fraud.
(Response) Virtual and/or remote inspections were not included in
the SOE proposed rule and AMS is therefore not setting specific policy
related to virtual or remote inspections. The final regulations provide
flexibility so that AMS may consider virtual inspection policy options
in the future.
Unannounced Inspections
(Comment) Several comments asked AMS to increase the minimum number
of operations that must receive unannounced inspections beyond the five
percent AMS proposed.
(Response) AMS is finalizing the proposed requirement that
certifying agents must conduct unannounced inspections of at least five
percent of the operations they certify. This is consistent with a 2011
NOSB recommendation and a current NOP Instruction document. AMS chose
this percentage because the majority of USDA-accredited certifying
agents currently complete unannounced inspections at this
frequency.\28\ Because most certifying agents are already completing
unannounced inspections at this level, this percent should be tenable
for certifying agents, regardless of size. To justify a higher
percentage, AMS would require additional information, industry
feedback, and data to assess the potential impact. Comments did not
provide justification or data to support a higher inspection
percentage. However, certifying agents may choose to conduct a higher
percentage of unannounced inspections to supplement their oversight and
enforcement of certified operations.
---------------------------------------------------------------------------
\28\ 42 of the 49 USDA-accredited certifying agents the NOP
audited in calendar years 2018 and 2019 completed unannounced
inspections for 5% of the operations they certify.
---------------------------------------------------------------------------
(Comment) Some public comments asked if AMS intends to publish
criteria for initiating or using unannounced inspections.
(Response) AMS is not adding criteria for using or initiating
unannounced inspections to the regulations. Unannounced inspections may
be triggered and selected by a variety of factors, including at random
and in response to complaints or investigations. The regulations
provide certifying agents flexibility to use unannounced inspections
when and where they are most effective.
Mass-Balances
(Comment) Several public comments asked if AMS is requiring one
mass-balance per certification scope (i.e., crops, livestock, handling,
wild crops) of an operation.
(Response) The regulatory text provides certifying agents the
flexibility to determine where such audits are most needed within a
single inspection.
(Comment) Some comments asked AMS if mass-balances should be
performed for single-ingredient or multi-ingredient products, and if
mass-balances for multi-ingredient products must balance all
ingredients in the product.
(Response) The final regulatory text provides certifying agents
flexibility to perform mass-balance audits of both single- and multi-
ingredient products. For multi-ingredient products, the certifying
agent may choose to mass-balance one or more of the ingredients.
E. Certificates of Organic Operation
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
[[Page 3574]]
------------------------------------------------------------------------
Section Final regulatory text
------------------------------------------------------------------------
205.2..................................... Terms defined.
Definition for Organic
Integrity Database.
205.404................................... Granting certification.
Paragraphs (b) and (c).
------------------------------------------------------------------------
Certificates of organic operation are an important tool used by
organic stakeholders to communicate information about certified
operations. Certifying agents must generate certificates of organic
operation electronically using the Organic Integrity Database.
Standardized, electronic certificates maintained in a publicly
accessible database will help to deter and prevent the use of
fraudulent certificates of organic operation. This requirement also
ensures that certificates of organic operation have consistent
information and format, allowing certifying agents and buyers of
organic products to readily validate certificates of organic operation.
Certifying agents may add their unique addenda to certificates of
organic operation to provide additional details about the certified
operation.
Affected entities may include certifying agents, applicants for
USDA accreditation, certified operations and entities seeking to
validate the certification status of an organic operation. Readers
should carefully examine the regulatory text and discussion below to
determine if they are affected by this action.
Background
AMS accredits nearly 80 certifying agents; only a few currently
create certificates of organic operation using the Organic Integrity
Database. As a result, more than 70 distinct formats of certificates of
organic operation exist in the market. This variation increases the
likelihood of alteration and organic fraud. In addition, AMS
consistently cites noncompliances for certifying agents who do not
include all of the required information on their certificates of
organic operation. Of the 49 USDA-accredited certifying agents audited
by the NOP in calendar years 2018 and 2019, 16 were cited for issuing
certificates of organic operation not consistent with USDA organic
regulations and instruction. The use of a uniform certificate of
organic operation generated through the Organic Integrity Database
eliminates these inconsistencies and helps avoid noncompliances.
The requirement for uniform certificates of organic operation
supports OFPA's purpose to facilitate interstate commerce of organic
foods (7 U.S.C. 6501(3)). This rulemaking also addresses a 2005 NOSB
recommendation to standardize information on certificates of organic
operation and require certifying agents to issue and maintain
certificates of organic operation from a common database.\29\
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\29\ NOSB Recommendation: Information on Certificates of Organic
Operation: https://www.ams.usda.gov/sites/default/files/media/NOSB%20Rec%20Standardize%20Organic%20Certifications%20Certificates.pdf.
---------------------------------------------------------------------------
Organic Integrity Database and Certificates of Organic Operation
The certificate of organic operation communicates information about
the organic certification of an operation. This rulemaking requires
certifying agents to provide uniform certificates of organic operation
that are electronically generated from the Organic Integrity Database.
AMS defines the term Organic Integrity Database in Sec. 205.2 as
the National Organic Program's electronic, web-based reporting tool for
the submission of data, completion of certificates of organic
operation, and other information, or its successors. The Organic
Integrity Database may also be referred to as the OID or INTEGRITY. AMS
is responsible for the functionality of the Organic Integrity Database
and ensuring consistent content and styles of all certificates of
organic operation. The general public can view information in the
Organic Integrity Database online at: https://organic.ams.usda.gov/integrity/
Generating Certificates of Organic Operation in the Organic Integrity
Database
Section 205.404(b) requires certifying agents to generate
certificates of organic operation in the Organic Integrity Database,
making it easier for the certificates to be accessed online by relevant
stakeholders in the organic supply chain (e.g., other certifying
agents, inspectors). Section 205.501(a)(15) requires certifying agents
to maintain current and accurate data on operations they certify in the
Organic Integrity Database. Together, sections 205.404(b) and
205.501(a)(15) require certifying agents to input and maintain accurate
data on the operations they certify, and to generate certificates of
organic operation using the Organic Integrity Database. This applies to
all USDA-accredited certifying agents whether foreign- or domestic-
based.
Certificates of organic operation generated in the Organic
Integrity Database include the required information that stakeholders
need to verify organic status of an operation. Users can also access
the database to see if an operation's organic certification has been
suspended, revoked, or surrendered. In addition to strengthening
organic integrity, standardized certificate format and data fields
facilitate and simplify verification of products, ingredients, and
suppliers. The Operation Profile feature in the Organic Integrity
Database also lists the generic products and services offered by an
operation. The accessibility and security of this data will reduce
administrative burden on certified operations that purchase organic
products and ingredients, as well as certifying agents and inspectors
who monitor compliance.
Certifying agents can continue using the data submission template
and the web-based form to upload the required data fields into the
Organic Integrity Database. Additionally, certifying agents can
transfer data from in-house databases to the Organic Integrity Database
using an Application Programing Interface (API) to reduce duplicative
data entry. AMS provides a data submission API guide for certifying
agents on the Organic Integrity Database's User Resources page.
Addenda to Certificates of Organic Operation
Some certifying agents use certificate addenda to supplement the
information on certificates of organic operation with more details
about an operation and the products it is certified to produce and/or
handle. Certificate addenda may be generated and maintained in the
Organic Integrity Database or by certifying agents' databases. The
rulemaking allows certifying agents to continue providing their own
certification addenda to communicate additional information about an
operation's certification in a different format than certificates
generated by the Organic Integrity Database. For example, an addendum
may include information about an operation's certification to
[[Page 3575]]
various international organic standards or the brand names of products
that the operation produces and/or handles that are not included on the
certificate of organic operation. Certificate addenda may be issued
only for a certified operation at an approved location(s).
Section 205.404(c) requires five elements to be on any organic
certificate addenda issued by certifying agents to deter organic fraud
and provide consistency across certifying agents. Primarily, the
addendum requirements are intended to ensure that someone viewing the
document is aware that certification may be verified in the Organic
Integrity Database. The accuracy of information on addenda, such as
products and labeling categories, may also be verified in the Organic
Integrity Database (see Operation Profiles). In summary, an addendum
must identify the name, location, and contact information of the
operation and certifying agent; an operation's unique operation ID from
the Organic Integrity Database; addendum issue date; a link to the
operation's certificate or profile in the Organic Integrity Database;
and a statement citing the Organic Integrity Database for certificate
verification. Certifying agents may include other data in addition to
the mandatory elements on certificate addenda.
Summary of Changes to the Final Rule
AMS revised Sec. 205.2 to replace the name of the proposed term
``INTEGRITY'' with ``the Organic Integrity Database.'' Additionally,
AMS did not include proposed Sec. 205.404(c)(6) which would have
required expiration dates on certificate addenda. Many public comments
noted that an addenda expiration date could cause confusion, as it
could be mistakenly interpreted as expiration of an operation's
certification. Organic certification does not expire; it continues
until surrendered, suspended, or revoked--see Sec. 205.404(d).
Further, several public comments noted that addenda expiration dates
would increase workload for certifying agents, as they would need to
update addenda expiration dates even if there are no other changes to a
certificate of organic operation. AMS agrees with public comments and
is not finalizing the requirement for addenda expiration dates. This
will also encourage stakeholders to adopt the best practice of
verifying certification status in the Organic Integrity Database, as
this tool will include the most up-to-date operation and certification
information (see Sec. 205.201(a)(15)).
Summary of Public Comments
Comments generally supported requirements to including uniform
information on certificates of organic operation, noting that this
would reduce inconsistencies across the industry on what information is
collected and maintained. Comments expressed concern about using the
Organic Integrity Database to generate the certificate files and some
argued that the proposed changes would instead hinder the process for
certificate generation, rather than streamlining it. Some certifying
agents noted that they would be more comfortable and efficient using
their proprietary databases to generate certificate information and
that using the Organic Integrity Database would be additional work to
enter duplicative data. Comments requested a method for certifying
agents to easily upload or transfer their existing data into the
Organic Integrity Database, and to generate a certificate of organic
operation. In addition, comments generally opposed including an
expiration date on certificates of organic operation because a
certificate expiration date could be conflated with an operation's
certification status.
Responses to Public Comment
(Comment) Comments requested that NOP change the name of the
proposed term INTEGRITY to Organic Integrity Database. Commenters
stated that referring to the database's nickname is not descriptive
enough and could lead to confusion between the concept of organic
integrity and the database.
(Response) AMS has revised Sec. 205.2 to use the term Organic
Integrity Database to reduce the possibility of stakeholder confusion
by using the full name of the database.
(Comment) Certifying agents stated that entering operation data
into their own databases and the Organic Integrity Database is
duplicative work and would be a financial and administrative burden
because it will require administrative staff to update both databases.
Commenters also expressed concern about whether the Organic Integrity
Database would have the functionality and capacity to withstand the
number of people who would need to access it regularly, if the Organic
Integrity Database is also used to generate certificates of organic
operation.
(Response) AMS provides tools for uploading data (data submission
template) and transferring data (via an API) into the Organic Integrity
Database to reduce duplication. Please see the data submission API
guide for certifying agents on the Organic Integrity Database's User
Resources page. In addition, generating certificates pulls from the
mandatory data that certifying agents must enter into the Organic
Integrity Database to comply with Sec. 205.501(a)(15). Section
205.501(a)(15) requires certifiers to enter data into the Organic
Integrity Database and states certifying agents must ``Maintain current
and accurate data in the Organic Integrity Database for each operation
which it certifies.'' Certificate generation does not require
additional data. AMS is prepared for the increased usage of the Organic
Integrity Database as a result of the rulemaking and will offer
outreach to certifying agents to support technology integration.
(Comment) AMS received comments requesting clarification on whether
the rule requires operations to receive certificates of organic
operation electronically--noting that many operations prefer (or can
only receive) paper certificates.
(Response) Section 205.404(b) states that an organic certificate
may be provided to operations electronically--however, this step occurs
after a certificate has been generated electronically and does not
affect how a certifying agent transmits certificates to an operation.
Anyone may print a certificate from the Organic Integrity Database as
needed.
F. Continuation of Certification
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.406............................................. Continuation of certification.
Paragraphs (a) and (b).
----------------------------------------------------------------------------------------------------------------
AMS has amended Sec. 205.406 to clarify the annual update
requirements for organic system plans (OSP) and to specify that
certifying agents are required to conduct inspections of operations
they certify at least once per
[[Page 3576]]
calendar year. These changes maintain requirements for certified
operations to provide certifying agents with updated and accurate
information about their organic activities while eliminating
duplicative work, and will strengthen oversight of organic operations
through regular and timely inspection. Affected entities may include,
but are not limited to certifying agents, certified organic operations,
and operations seeking organic certification. You should carefully
examine the regulatory text to determine if you or your organization
may be affected by this action.
Annual Updates of Organic System Plans
Previously, the organic regulations required certified operations
to submit an updated OSP in its entirety as part of annual
certification renewal. Certifying agents implemented this
inconsistently: some required certified operations submit an entire OSP
every year, while others required operations only to submit revisions
to their OSP. To clarify OSP requirements, this rulemaking revises
Sec. 205.406(a) to allow certified organic operations to only submit
sections of its OSP that have changed to its certifying agent.
Additionally, the rulemaking removes previous paragraph Sec.
205.406(a)(3), which required that certified operations provide, along
with its annual update, an update on the correction of minor
noncompliances previously identified by the certifying agent as
requiring correction for continued certification. This requirement was
duplicative and unnecessary, as certifying agents (when issuing a
notice of noncompliance) must specify a date by which a certified
operation must rebut or correct noncompliances (Sec. Sec.
205.662(a)(3) and 205.404(a)). Removal of this requirement reduces
paperwork, simplifies the certification process, and ensures that
noncompliances are resolved according to the deadline in the notice,
rather than waiting until the next certification cycle.
The NOP previously described this approach in published certifying
agent Instructions (NOP 2615 and NOP 2601).\30\ This change is
necessary to ensure legal enforceability, consistent practices between
certifying agents, and reduce the paperwork burden of organic
certification. This will not impact the requirements for certified
operations to maintain an updated OSP or the requirement for an
operation to notify its certifying agent of operational changes that
may affect its compliance with organic regulations (Sec. 205.400(f)).
Further, the on-site inspection of an organic operation must verify
that the entire OSP is implemented as described.
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\30\ NOP 2601 The Organic Certification Process, December 16,
2013: https://www.ams.usda.gov/sites/default/files/media/2601.pdf;
NOP 2615 Organic System Plans, Organic System Plan Updates, and
Notification of Changes, December 16, 2013: https://www.ams.usda.gov/sites/default/files/media/2615.pdf.
---------------------------------------------------------------------------
Frequency and Scheduling for Annual Inspections
Annual inspection cycles are essential to vigilant oversight of
organic operations. Inconsistent interpretation of previous Sec.
205.406 regarding inspection timing sometimes resulted in inspection
frequencies longer than the annual timeframe specified in OFPA (7
U.S.C. 6506(a)(5)). For example, former Sec. 205.406(b) was sometimes
interpreted to mean that an operation may be inspected once every 18
months on an ongoing basis (i.e., two inspections over a 36-month
period compared to three inspections if conducted annually). To clarify
frequency of on-site inspection, this rulemaking revises Sec.
205.406(b) to simplify the regulatory text and clearly state that
inspections are to be conducted at least once per calendar year.
Revised paragraph (b) clarifies that all certified operations must
be inspected at least once in a calendar year, regardless of (1) when
the certified operation was last inspected and (2) when, or if, the
certified operation provided its annual updates. This revision allows
certifying agents flexibility to conduct on-site inspections at any
time during the year (essential for verifying activities throughout the
growing season, for example) to ensure that an inspection is conducted
every single calendar year. Additional inspections may be needed to
inspect all portions of an operation to assess full compliance of an
operation (e.g., during and outside the grazing season for livestock
operations). This requirement does not replace the need for additional
unannounced inspections.
Summary of Changes to the Final Rule
AMS did not make any revisions to the proposed regulatory text. The
policy continues unchanged in this final rule.
Summary of Public Comment
Public comments largely supported changes made in the proposed
rule, citing support for reduced paperwork, increased flexibility, and
clear enforceability to uphold organic integrity. Some comments
questioned the need for the proposed changes, citing that the work of
updating an entire OSP is not significantly greater than updating
portions of it.
Several comments supported revisions to section 205.406(b), which
now requires certifying agents to conduct on-site inspection once per
calendar year. However, commenters requested additional flexibility
regarding annual inspections requirements in the face of extreme
circumstances that may render an in-person inspection unsafe or
unfeasible for the inspector or operation. These comments cite the
COVID-19 pandemic as an example.
Other comments were generally in support of the flexibility that
the revisions provide, particularly allowing inspections to occur when
seasonally appropriate (and potentially reducing certifying agents'
need to request additional inspections). However, a few commenters
noted that the calendar year restriction may cause inspections to occur
one closely after another, depending on the type of operation and
harvest timeline.
Responses to Public Comment
(Comment) AMS received comments stating that the revisions to OSP
submission requirements could lead to inconsistent information across
certifying agent databases and the Organic Integrity Database.
(Response) All certifying agents are now required to maintain
updated information on operations they certify in the Organic Integrity
Database. This requirement will eliminate inconsistencies.
(Comment) Comments asked if certifying agents can still request
full updated OSPs from operations they certify, should the certifying
agent deem the proposed changes significant.
(Response) The rulemaking does not change or limit the ability of
certifying agents to request information, including a full OSP, that is
needed to determine an operation's compliance with the organic
regulations. Paragraph 205.406(a)(4) of the regulations requires
operations to provide certifying agents information that they deem
necessary to determine compliance with organic regulations.
(Comment) We received comments requesting more flexibility
regarding annual inspections (e.g., allowing the issuance of temporary
variances, or allowing for virtual inspections) in the face of extreme
circumstances that may render an in-person inspection unsafe or
unfeasible for the inspector or operation.
(Response) AMS acknowledges that extreme circumstances may prevent
a certifying agent from completing an on-site inspection once per
calendar year. In such cases, the certifying agent may
[[Page 3577]]
delay inspection, but the delay should be minimized and explained in
the certifying agent's inspection report and records. A certifying
agent's inability to consistently inspect operations annually due to
access, safety, extreme weather, or other issues is a failure to carry
out inspection requirements and does not fulfill the general
requirements for accreditation (Sec. 205.501(a)(3)). When the
certifying agent is unable to provide adequate oversight and
enforcement, the certifying agent should not continue to certify the
operation.
(Comment) AMS received comments proposing an inspection window
anywhere between 7 and 17 months apart rather than 18 months, thus
allowing inspectors to conduct inspections when seasonally appropriate.
(Response) The rulemaking establishes a minimum frequency for on-
site inspections--at least once per calendar year--to ensure all
certified operations meet OFPA's requirement for annual inspection. If
the certifying agent is unable to complete a full inspection during a
time when land, facilities, and activities that demonstrate compliance
can be observed (see Sec. 205.403(c)(2)), then the certifying agent
may conduct additional on-site inspections, as allowed in Sec.
205.403(a)(3)(i), to cover unobserved portions and ensure compliance
with Sec. 205.403.
G. Paperwork Submissions to the Administrator
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.501............................................. General requirements for accreditation.
Paragraph (a)(15).
----------------------------------------------------------------------------------------------------------------
Accurate and current information about certified operations is
critical for commerce and oversight in the organic sector. This
rulemaking supports accessible and updated data on organic operations
by requiring certifying agents to maintain current data on all
operations they certify in the Organic Integrity Database. Certifying
agents and certified operations may be affected by these requirements.
Readers should carefully review the regulations and policy discussion
to determine whether they must comply.
Background
The organic industry, including certifying agents, certified
operations, consumers, AMS, and other regulatory agencies use the
Organic Integrity Database to confirm the certification status of
operations, organic status of products, find contact or product
information for specific operations, and obtain data points for
investigation and enforcement actions. Timely updates to maintain data
on an operation's current status, including certified products and
acreage, is necessary for efficient business transactions and informed
oversight. The availability of operation data also reduces the time
spent by certifying agents and by AMS responding to inquiries about
specific operations because interested parties can independently access
the information they need.
Mandatory Reporting in Organic Integrity Database
Certifying agents are required to provide and maintain current
mandatory data on operations in the Organic Integrity Database. The
required data fields are listed in the INTEGRITY Data Dictionary and
defined in the Glossary of Terms which can be accessed at https://organic.ams.usda.gov/Integrity/About.aspx. Some of the data in the
Organic Integrity Database is publicly accessible. Examples of
mandatory, public data fields include: certification status, scope(s)
of certification (e.g., crops, livestock, handling, wild-crop), and the
organic commodities produced or handled by the operation. This
information is essential for certifying agents and operations to verify
the organic status of operations and products and supports efficient
business transactions. Organic acreage is an example of mandatory data
that will not be publicly available in the Organic Integrity Database.
Update Frequency
Certifying agents are to establish processes for updating data in
the Organic Integrity Database in a manner that keeps information
current about their certified operations. This is needed to support the
industry's reliance on the Organic Integrity Database for current and
accurate information about individual operations. Certifying agents are
required in Sec. 205.662(e)(3) to update the Organic Integrity
Database within 72 hours of an operation's suspension, revocation or
surrender of certification.
This rule removes the requirement for certifying agents to provide
notices of denial of certification to the Administrator following the
issuance of a notice of noncompliance to an applicant for certification
(formerly Sec. 205.405(c)). In addition, the rule removes the
requirement for submission of any notices of denial of certification,
notifications of noncompliance, notification of noncompliance
correction, notification of proposed suspension or revocation, or
notification of suspension or revocation (formerly Sec.
205.501(a)(15)(i)). Also, the rule removes the annual requirement for
certifying agents to submit, by January 2, an annual list of operations
certified during the preceding year (formerly Sec.
205.501(a)(15)(ii)). Certifying agents' adherence to noncompliance
procedures in the regulations are evaluated during NOP audits, review
of appeal cases and relevant complaints. The requirement for certifying
agents to list operations in the Organic Integrity Database and their
corresponding certification status makes the paperwork submission
requirements unnecessary.
Summary of Changes to the Final Rule
AMS renamed the term INTEGRITY in Sec. 205.501(a)(15) to the
Organic Integrity Database.
Summary of Public Comment
Comments were largely in support of the proposed revisions, citing
that the changes remove an unnecessary and redundant step from
certifying agents' day-to-day operations. Commenters also noted that
codifying global use of the Organic Integrity Database and maintaining
``accurate and current'' data are both critical to ensuring organic
integrity. Commenters noted that the regulatory text does not explain
how often certifying agents should update operation data.
Responses to Public Comment
(Comment) Comments requested that AMS require certifying agents to
upload and maintain data in the Organic Integrity Database on
operations that are no longer certified, were denied certification, or
withdrew certification with adverse actions on record.
(Response) The Organic Integrity Database can identify applicants
for certification that were denied or
[[Page 3578]]
withdrew from certification. AMS encourages certifying agents to enter
those operations into the Organic Integrity Database, however, this is
not a required reporting element. The Organic Integrity Database
includes all operations which are no longer certified because they are
suspended, revoked, or surrendered.
(Comment) Comments noted that the rule does not describe the data
fields that certifying agents are required to complete in the Organic
Integrity Database.
(Response) The Data Dictionary provides a list of all data fields
for the Organic Integrity Database (https://organic.ams.usda.gov/Integrity/About.aspx). The Data Dictionary will be updated upon
implementation of this rulemaking to make all current fields mandatory.
AMS may add more mandatory fields in the future based on industry and
NOP needs.
(Comment) Comments requested that certifying agents be required to
update the Organic Integrity Database within 72 hours of any changes to
crops, products, acreage, or certification status.
(Response) The rule does not require certifying agents to update
all required data fields within a certain timeframe, as certifiers need
flexibility to create their own systems for updating and maintaining
current data in the Organic Integrity Database. However, AMS does
require certifying agents to update certain data fields within a
specified timeframe. For example, Sec. 205.662(e)(3) requires
certifying agents to update the Organic Integrity Database with changes
to an operations certification status within 3 business days. The Data
Quality Minimum Standards and Best Practices provides recommendations
for the minimum frequency to update specific data fields in the Organic
Integrity Database.\31\
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\31\ Available in the Organic Integrity Database: https://organic.ams.usda.gov/integrity/About.aspx.
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H. Personnel Training and Qualifications
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definition for Certification review.
205.501............................................. General requirements for accreditation.
Paragraphs (a)(4), (5), and (6).
----------------------------------------------------------------------------------------------------------------
The USDA organic regulations require that certifying agents use a
sufficient number of trained and qualified inspectors and certification
review personnel with expertise in organic production and handling.
This rulemaking enhances existing requirements with detail about the
qualifications that organic inspectors and certification reviewers must
have in order to work for certifying agents. By clarifying the
necessary technical skills, qualifications, and knowledge needed to
conduct organic inspections and certification review, AMS ensures that
inspectors and certification reviewers are better prepared to verify
organic compliance, which further strengthens organic integrity across
all levels of the supply chain and upholds confidence in the organic
label among consumers.
The rule adds new requirements for certifying agents, inspectors,
and certification personnel:
Certifying agents must verify that all inspectors and
certification personnel they contract with or hire have the minimum
required training, skills, and knowledge.
Inspectors and certification personnel must meet a minimum
baseline of knowledge, skills, and experience before beginning
inspection or certification review activities.
Inspectors and certification personnel must meet annual
training requirements to continue inspection or certification review
activities.
Certifying agents must conduct periodic observations of
inspectors during inspections (``witness inspections'') as a part of
their annual evaluation activities.
Certifying agents must maintain policies, procedures, and
records regarding inspector and certification review personnel training
and evaluation.
The provisions in this chapter affect current and potential organic
inspectors, certification review personnel, and certifying agents who
employ or contract with inspectors or certification review personnel.
Some provisions apply directly to certifying agents' hiring and
evaluation processes. Others clarify the amount of training inspectors
are required to do to maintain compliance to the organic regulations.
The following discussion provides further detail on the provisions and
AMS's responses to comments received on the proposed rule.
Background
To continue certification, a certified organic operation must
undergo an on-site inspection at least once a year. Organic inspectors
visit certified organic operations to thoroughly investigate the
operation's processes, facilities, and records. Inspections vary by
type and complexity of operation, but generally an inspector will
review fields to investigate pest management, soil fertility
management, buffer zones, and other production techniques; inspect
storage and preparation areas for evidence of commingling or
contamination with substances prohibited in organic; review records and
invoices; conduct mass-balance, traceability, and yield analyses; and
interview a representative of the operation. The inspector may also
collect samples to test for pesticide residues. The inspector then
prepares an inspection report that the certifying agent uses to
evaluate the operation's compliance with the organic regulations. In
addition to regular, once-a-year scheduled inspections, organic
inspectors also conduct unannounced inspections, which are conducted
without advance notice and are often used to target a more limited, but
higher-risk, portion of an operation to ensure compliance (see the
``On-Site Inspections'' portion of this rule for more detail).
Organic inspectors and review staff are therefore the most direct
form of enforcement and verification because they inspect certified
organic operations onsite and report their findings to certifying
agents. Persons performing certification review activities also ensure
organic integrity by reviewing these inspection reports along with
organic system plans, inputs, and other certification documents that
are used to determine compliance with the organic regulations and grant
continued certification. The role as inspectors and
[[Page 3579]]
reviewers has only grown more critical as organic operations and supply
chains become more complex and diverse.
Inspection and certification review are complex professions that
require detailed and highly specialized knowledge of organic regulation
and agricultural practices and strong observation, communication, and
investigation skills. Without highly qualified inspectors and
certification review personnel, loss of organic integrity--either
unintentional or fraudulent--would go unnoticed and the organic
certification system would fail. Therefore, these personnel must adhere
to consistent standards of knowledge, skill, and experience, relevant
to the scope and complexity of the organic operations they inspect and
review. Consistent standards will ensure effective oversight and review
of organic operations, catching and preventing mishandling and fraud at
critical points in the organic supply chain.
The rapidly increased complexity and scale of the organic market
has multiplied opportunities for mishandling of organic products and
fraud, especially as supply chains for organic products increasingly
depend on imported goods. In its February 2018 recommendation, the NOSB
referenced ``well-publicized incidents of proven fraudulent imports in
the last year'' as a compelling reason to ensure the industry has
``qualified inspectors experienced in a broad range of operations
diverse in scope and scale.'' \32\ For example, a May 2017 Washington
Post investigation found that millions of pounds of imported corn,
soybeans, and ginger had been fraudulently labeled organic, and
inconsistent inspection practices were partly to blame.\33\
Additionally, public comments from accredited certifying agents and
organic inspector associations agreed that minimum training and
qualification requirements for inspectors are necessary to detect
breach of organic integrity and fraud. AMS recognizes that in a diverse
market where operations can choose their own certifiers, one critical
element of protecting organic integrity and preventing fraud is
ensuring that all organic inspectors and reviewers are held to the same
high standards of training and experience.
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\32\ NOSB Formal Recommendation, Inspector Qualifications and
Training, May 29, 2018: https://www.ams.usda.gov/sites/default/files/media/CACSInspectorQualificationsRec.pdf.
\33\ Peter Whoriskey, ``The labels said `organic.' But these
massive imports of corn and soybeans weren't.'' Washington Post. May
12, 2017. https://www.washingtonpost.com/business/economy/the-labels-said-organic-but-these-massive-imports-of-corn-and-soybeans-werent/2017/05/12/6d165984-2b76-11e7-a616-d7c8a68c1a66_story.html?utm_term=.97e7f3942427&itid=lk_inline_manual_
7.
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The regulations previously lacked specific detail about
qualifications, experience, and continual training for inspectors and
certification reviewers. Certifying agents currently set their own
policies and minimum qualifications to hire inspectors and reviewers,
creating inconsistency in on-site inspection and certification review.
Further, many inspectors are independent contractors who are
responsible for establishing and maintaining their own knowledge base.
This diversity of background and training creates an inconsistent
baseline of knowledge and skill.
In 2012, NOP issued a memo to clarify that all inspectors and
reviewers, whether staff or independent contractors, must possess the
expertise and qualifications needed to evaluate compliance with the
USDA organic standards.\34\ Additionally, the NOSB provided
recommendations in 2018 to address the need for specific qualification
and training requirements for inspectors and persons performing
certification review.\35\ This rulemaking codifies the general policy
in the 2012 memo and addresses the NOSB recommendations by describing
baseline qualifications for certifying agent personnel.
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\34\ NOP Memo: Criteria and Qualifications for Organic
Inspectors; April 2012: https://www.ams.usda.gov/sites/default/files/media/NOP-Notice-OrganicInspectorCriteria.pdf.
\35\ NOSB Formal Recommendation, Inspector Qualifications and
Training, May 29, 2018: https://www.ams.usda.gov/sites/default/files/media/CACSInspectorQualificationsRec.pdf.
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To clarify the portions of this policy that apply to certification
review personnel, AMS defines the term certification review as ``the
act of reviewing and evaluating a certified operation or applicant for
certification and determining compliance or ability to comply with the
USDA organic regulations.'' The term does not encompass performing an
inspection, which is separately defined in Sec. 205.2.\36\ Examples of
certification review includes reviewing applications for certification,
reviewing certification documents, evaluating qualifications for
certification, making recommendations concerning certification, or
making certification decisions and implementing measures to correct any
deficiencies in certification services. Establishing baseline
qualifications for the personnel conducting these activities will lead
to greater consistency in certification review and decision.
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\36\ Sec. 205.2 Inspection. The act of examining and evaluating
the production or handling operation of an applicant for
certification or certified operation to determine compliance with
the Act and the regulations in this part.
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General Requirements
Section 205.501(a)(4) requires that certifying agents
``continuously use a sufficient number of qualified and adequately
trained personnel'' to implement and comply with the organic
regulations. Certifying agents must maintain adequate staffing levels
and the range of expertise needed to perform the full range of
certification activities, including inspection and certification
review. This includes maintaining an inspection staff to timely
complete initial on-site inspections, annual inspections for all
operations it certifies, unannounced inspections on a minimum of 5
percent of the operations it certifies annually (see Sec. 205.403(b)),
and any other inspections needed to ensure compliance with the
regulations.
Certifying agents sometimes use contracted or volunteer personnel
(i.e., persons not directly employed by the certifying agent) to
inspect operations or complete certification review. Therefore,
certifying agents must ensure that all inspectors and certification
review personnel--including staff, contractors, and volunteers--meet
the requirements of Sec. 205.501(a)(4)-(6). This means that any person
performing inspection or certification review activities must meet
these requirements, regardless of their work or contractual
relationship with the certifying agent. This ensures consistent
inspection and certification review by all certifying agents.
Knowledge, Skill, and Expertise
Certifying agents must demonstrate that all personnel they use to
conduct inspection and certification review continuously maintain
knowledge and skills that qualify them to perform duties as assigned
(Sec. 205.501(a)(4)(i)(A) and (a)(4)(ii)(A)). These paragraphs detail
the minimum knowledge and skills that inspectors and certification
reviewers must have. Because inspectors and certification reviewers
perform different functions, each must meet different baseline
criteria, although there is some overlap, such as knowledge and skill
of the organic regulations, traceability audits, and mass-balance
audits. Certifying agents must demonstrate, as part of their
accreditation process, that any inspectors or certification reviewers
they use have sufficient knowledge in organic standards and practices
to successfully understand, verify, and document an operation's
compliance or noncompliance with the organic regulations.
[[Page 3580]]
The requirements in the rulemaking are based on NOSB
recommendations, public comments, and the NOP's own experience auditing
certifying agents. AMS chose these specific skills because they are
essential to inspection and certification review. These requirements
will ensure that inspectors and certification review personnel can
accurately interpret the regulations and standards, and consistently
apply critical skills when inspecting and assessing compliance. This
will address the current regulation's lack of specific qualifications,
experience, and continual training for inspectors and reviewers.
Certifying agents must also demonstrate the expertise of all
personnel they use to conduct inspection and certification review
(Sec. 205.501(a)(5)). Critically, this means all inspection and review
personnel must have expertise in knowledge of certification to the USDA
organic standards. Certifying agents must also demonstrate their
personnel must have education, training, or professional experience in
the fields of agriculture, science, or organic production and handling
that relates to assigned duties. This requirement to demonstrate
expertise will facilitate more robust accreditation audits of
certifying agents and ensure more consistent oversight of certifying
agents. Together with the above knowledge and skills, this requirement
to maintain adequate expertise will also promote development of a
uniform, high-quality base of organic inspectors and certification
reviewers.
Training
Organic inspectors and certification reviewers must complete
regular training relevant to their duties. Training may include
courses, webinars, training sessions, field days, seminars,
conferences, shadowing other inspectors on their inspections, and
directed readings on relevant topics. Certifying agents may determine
if specific trainings fulfill the requirements. Relevant training
courses available on the Organic Integrity Learning Center (OILC) may
also meet the annual training requirements. When the minimum training
hours are completed, certifying agents must still ensure that each
inspector and certification reviewer has the training that is
sufficient to competently perform assigned inspections or duties.
Sections 205.501(a)(4)(i)(B) and 205.501(a)(4)(ii)(B) require
inspectors and certification review personnel with less than one year
of experience to complete at least 50 hours of training on USDA organic
standards, inspection protocols, and organic production and handling
practices. This requirement will help ensure new inspectors and
certification review personnel are adequately prepared for their
duties. The proposed rule had included a lower number of hours across
all staff, new and experienced. Commenters suggested that less-
experienced staff require more hours of training than existing staff.
AMS agrees with public comments and has raised the initial training
requirement for less-experienced staff to 50 hours, which is a
reasonable balance that aligns with industry best practice and will
ensure staff are adequately prepared to perform inspection and
certification duties.
Onboarding for new inspectors or certification reviewers hired by
certifying agents may count towards the 50-hour requirement, as can
other qualifying training they complete in their first year performing
inspection or certification review duties. Any onboarding that counts
towards the training would need to be technical rather than
administrative to qualify as relevant training. New inspectors must
complete the 50 hours of training, at minimum, before they conduct
inspections independently. This allows new inspectors to gain practical
training through shadow inspections. Training requirements apply
equally to inspectors who are hired as employees and contractors of
certifying agents; initial training received must sufficiently address
the scope and complexity of work these personnel encounter when
performing their duties.
Sections 205.501(a)(4)(i)(B) and 205.501(a)(4)(ii)(B) detail
training requirements for inspectors and certification reviewers with
more than one year of experience. Inspectors and certification
reviewers must complete relevant ongoing training appropriate to their
existing skills, expertise, and scope of work. The annual minimum is 10
hours per year for personnel inspecting or reviewing one area of
operation (i.e., crops, wild crops, livestock, and handling). Five
additional hours of annual training are required for each additional
scope or area of operation. For example, an inspector who only inspects
crop operations (i.e., a single area of operation) must complete at
least 10 hours of annual training; an inspector who inspects crop,
livestock, and wild crop operations (i.e., three areas of operation)
must complete at least 20 hours of training annually. Because there are
four scopes of certification in the USDA organic regulation (crops,
livestock, handling, and wild crops), the maximum number of training
hours an inspector would be required to complete annually would be 25
hours (10 hours of training for the first scope of certification, plus
5 hours for each of the additional 3 scopes of certification).
AMS chose these training requirements based on review of public
comment and review of established industry norms. AMS agrees with
public comments that new inspectors will require more robust initial
training and certifying agent personnel may require more or less annual
training depending on how many areas of operation they inspect or
review. Therefore, relative to the proposed rule, AMS is requiring 50
hours of training for new personnel, and 10 hours plus 5 hours per
additional area of operation for more experienced inspectors.
AMS chose the 50-hour requirement for new inspectors because it
aligns with industry best practice. Some certifying agents commented
that the proposed 20-hour requirement for new inspectors was adequate,
while others maintained that 75-100 hours was necessary; 50 hours is a
median within that range. The 50-hour requirement also aligns closely
with the Accredited Certifier's Association's ``Guidance on Organic
Inspector Qualifications,'' which recommends initial inspector training
that totals 43-46 hours plus several mentored inspections and monitored
reports.\37\ Finally, many certifying agents currently require new
inspectors to complete the International Organic Inspector
Association's (IOIA) basic training, a 5-day course requiring
approximately 40 hours to complete,\38\ plus additional field
observation and training that together total to 50 hours of training.
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\37\ ``Guidance on Organic Inspector Qualifications,''
Accredited Certifiers Association, Inc., February, 2018, https://www.accreditedcertifiers.org/wp-content/uploads/2018/02/ACA-Guidance-on-Inspector-Qualifications-with-IOIA-Evaluation-Checklist.pdf.
\38\ IOIA Basic Training: https://www.ioia.net/training-program-overview/.
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AMS chose an annual training requirement of 10 hours plus 5 hours
per additional scope for more experienced inspectors because it is
consistent with standards established by other agencies or
organizations (e.g., Preventive Controls Qualified Individuals per 2011
Food Safety Modernization Act, ISO 9001 Global Certified Lead Auditor),
and because it increases flexibility by allowing more or less total
annual training hours based on the areas of operations inspected or
reviewed. These requirements will ensure that inspectors and reviewers
receive annual training that is
[[Page 3581]]
appropriate for the level and scope of their duties.
In certain cases, certifying agents may not be able to prescribe
specific training to contracted inspectors or certification review
personnel. However, certifying agents must use a sufficient number of
qualified and trained personnel (Sec. 205.501(a)(4)) and demonstrate
that all persons with inspection and certification review
responsibilities have expertise in organic production and handling
(Sec. 205.501(a)(5). This means that certifying agents must ensure any
contractor used to conduct inspection or certification review
activities meets the training requirements described in the regulation.
Experience
In addition to training, Sec. 205.501(a)(4)(i)(C) requires that
certifying agents demonstrate that the inspectors they use have
experience that prepares them to conduct their assigned duties.
Certifying agents must demonstrate that inspectors have at least 2,000
hours of relevant experience that prepares them for the areas of
operation they will be assigned (i.e., crops, livestock, handling, or
wild crops). Both this baseline experience requirement and the 50-hour
training requirement must be met before inspectors can independently
inspect organic operations. An experienced inspector may advance to
inspect more complex operations based on performance.
The proposed rule specified one year of experience. This was
consistent with the 2018 NOSB recommendation and generally supported by
public comments. However, because public comments noted that ``one
year'' is unclear and can be interpreted differently, AMS has chosen a
more specific 2,000-hour requirement. This is equivalent to one year of
full-time work (accounting for vacation and time off) and expands the
pool of qualifying experiences because the hours can be obtained across
multiple years, from one or more jobs, internships, or other qualifying
activities.
Eligible types of experience include but are not limited to: work
on a farm or ranch; agricultural extension work; agricultural
education; internships; apprenticeships; experiential education; 4-H;
Future Farmers of America; other inspection or auditing work;
management of an organic food handling operation; food processing
research; or natural resource management work. Qualifying experience is
not restricted to paid work, and may include volunteer work or
education.
This minimum experience requirement is supported by Sec.
205.501(a)(5), which requires that certifying agents demonstrate that
all persons with inspection or certification review responsibilities
have education, training, or professional experience that relates to
the duties they will perform.
Field Evaluation of Inspectors
Section 205.501(a)(6) requires certifying agents to ensure that
every inspector they use is evaluated while performing an inspection at
least every three years. Inspectors with less than three years of
organic inspection experience must be evaluated every year. The
regulatory text refers to observing an inspector while they are
inspecting an operation as a ``witness inspection.'' This term is used
by the International Standards Organization to refer to observations of
inspections to ensure proper adherence to inspection procedures and the
standards to which the inspection is being made.
The rulemaking's field evaluation requirements are consistent with
a 2016 NOSB proposal and accepted industry guidance from the Accredited
Certifiers Association.\39\ In addition, public comments supported this
evaluation frequency, including annual evaluations for inspectors with
less than three years of inspection experience. The rulemaking is
therefore aligned with industry best practice, and will ensure that the
performance of all inspectors is consistently monitored and evaluated
by certifying agents.
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\39\ ``Personnel Performance Evaluations of Inspectors''
proposal, December 13, 2016: https://www.ams.usda.gov/sites/default/files/media/CACSInspectorsProposal.pdf.
The Accredited Certifiers Association, Inc. is a 501(c)(3) non-
profit educational organization created to benefit the accredited
organic certifying agent community and the organic industry: https://www.accreditedcertifiers.org/.
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The above requirement is a minimum and certifying agents have the
option of conducting witness inspections more frequently than the above
guidelines to verify an inspector's ability to successfully conduct
inspection duties. For example, certifying agents may decide to conduct
additional witness inspections if there is a sudden change in the
complexity of an operation being inspected, or if inspection reports
show deficiencies in an inspector's skill or knowledge.
To ease the burden on certifying agents and inspectors, certifying
agents may share witness inspection reports with each other, but each
certifying agent must demonstrate that they have evaluated each
inspector's performance in accordance with their own internal personnel
policies and procedures. Certifying agents may use employees or
contractors to perform the witness inspections, provided they are
qualified to perform such duties (e.g., a witness inspection for a
diversified crop operation should be overseen by an evaluator with
adequate experience in inspecting diversified crop operations). A key
indicator of an individual's qualifications to conduct witness
inspections is whether that person can perform the type of inspections
they are evaluating.
To ensure that witness inspections are effective and consistent,
certifying agents must maintain procedures for conducting and
documenting them, and maintain records of all witness inspections of
inspectors they have conducted (Sec. 205.501(a)(6)(ii)). These records
may include a quantitative or qualitative evaluation of the inspector,
along with details on where, when, by whom, and on what area of
operation the inspection was conducted. This requirement will
facilitate more robust accreditation audits and ensure more consistent
oversight of certifying agents.
Witness inspections are intended as one tool to help certifying
agents maintain, evaluate and improve inspector quality, but certifying
agents are also expected to take corrective action appropriate to
remedying gaps and deficiencies in knowledge and skills. For example,
if a witness inspection identifies problems with an inspector's report
writing, then a desk audit of additional inspection reports may be
appropriate to address any shortcomings. Conversely, if an inspector
misses a significant noncompliance while inspecting an operation, the
certifying agent may decide to conduct a follow-up witness inspection
of the inspector.
Summary of Changes to the Final Rule
AMS made several changes to the proposed regulatory text when
writing this final rule. Changes to the final rule are discussed below
and are followed by responses to specific themes from public comment.
In Sec. 205.501(a)(4)(i) and (a)(4)(ii), AMS changed
``scale'' to ``complexity'' because public comments noted that scale
does not always equate to greater complexity. AMS agrees with public
comments and included ``complexity'' in the rulemaking to highlight its
importance in determining appropriate qualifications for inspectors and
reviewers.
In Sec. 205.501(a)(4)(i)(A) and (a)(4)(ii)(A), AMS
replaced ``auditing'' with ``traceability audits'' and ``mass-balance
audits.'' This addresses public
[[Page 3582]]
comments that requested additional specificity about the meaning of
``audit.'' The new language more closely aligns with accepted and well-
understood industry terminology and more clearly describes the
knowledge and skills that certifying agents must ensure their
inspectors and reviewers possess.
AMS revised the proposed annual training requirement of 20
hours in Sec. 205.501(4)(i)(B) and (4)(ii)(B). Inspectors and
reviewers must complete a baseline of 10 hours of training, plus an
additional 5 hours for each additional area of operation they inspect
or review. Inspectors and reviewers with less than one year of
inspection experience must complete 50 hours of training within their
first year. This revised requirement is consistent with established
industry training standards but is also more flexible because it allows
for more or less total annual training hours based on the experience of
the inspector or reviewer and the areas of operations they inspect or
review. This requirement will ensure that inspectors and reviewers
receive annual training that is appropriate for the level and scope of
their duties.
AMS updated proposed Sec. 205.501(a)(4)(i)(C) from
``field-based experience related to both the scope and scale of
operations they will inspect'' to ``experience relevant to the scope
and complexity of operations they will inspect.'' We removed ``field-
based'' because that term was unclear and could be interpreted too
narrowly. Using ``scope and complexity'' focuses the requirement on
experience relevant to the type of inspections to be performed.
AMS changed the one-year experience requirement in Sec.
205.501(a)(4)(i)(C) to 2,000 hours in response to comments that
requested more specificity and a clear metric for verifying compliance.
A 2,000-hour requirement is clearer, will promote consistent
implementation among certifying agents, will allow inspectors to
combine qualifying experience from more than one activity, and was
supported by public comments.
In Sec. 205.501(a)(6), AMS added ``witness inspection''
to refer to certifying agents observing inspectors as they inspect an
operation. This change aligns with industry and international
convention and more clearly describes the requirement.
AMS revised Sec. 205.501(a)(6) to clarify that certifying
agents must conduct annual witness inspections of inspectors with fewer
than three years of experience. This change is consistent with industry
best practice and will ensure that the performance of new inspectors is
consistently monitored and evaluated by certifying agents.
Summary of Public Comment
Many public comments focused on the proposed number of required
hours of continuing education, with a mix of comments that believed
that 20 hours annually is sufficient, and others arguing that 20 hours
would not be sufficient. A few comments requested flexibility in how
inspectors meet the education requirements, suggesting that added
flexibility would help them complete the education more easily and
reduce costs for certifying agents.
Some comments expressed concern that the proposed requirement of
one-year of field-based experience was restrictive, and that the
proposed rule was not specific enough about what types of experience
would qualify. AMS also received several comments noting that using
years as a metric is not an adequate measure for experience; several
comments suggested a minimum number of hours per year as an
alternative.
Several comments discussed inspector evaluations, with most of
these comments supporting in-person evaluations once every three years,
and others recommending more frequent evaluations for new or
inexperienced inspectors.
Responses to Public Comment
Specified Additional Knowledge, Skills, and Experience
(Comment) One comment stated that labor laws prevent certifying
agents from requiring contract inspectors to undertake specific
training.
(Response) The regulations do not require contract inspectors to
complete training specified by certifying agents; however, certifying
agents must demonstrate that all inspectors, including contract
inspectors, complete training that is relevant to inspection.
Certifying agents can recommend or offer courses to contract
inspectors, but may not be able to require completion of specific
training courses. Certifying agents should review inspector training
logs or other records to ensure that the inspector has completed the
required number of hours and that the training is appropriate to
inspectors' skill and role.
(Comment) Comments expressed concern that a list of skills,
knowledge, and experience detailed in Sec. 205.501(a)(4)(i)(A) may
limit the pool of organic inspectors, and thus limit the capacity of
certifying agents to inspect operations. Comments stated that specific
qualifications should be based on the scope of inspections performed by
individual inspectors.
(Response) The list of qualifications specified in this section are
not unique to any specific type of organic operation, but are important
for all inspection and certification review activities, regardless of
area of operation. All inspectors must meet the general qualifications
listed in Sec. 205.501(a)(4)(i)(A). Specific qualifications should be
based on the scope of inspections performed--Sec. 205.501(a)(4)
requires certifying agents to demonstrate that inspectors have
qualifications to inspect the scope and complexity of the operations
assigned.
(Comment) Comments recommended including recordkeeping, mass-
balance audits, traceability/trace-back audits, DMI calculations,
biosecurity, cultural training, and internal control systems for
producer groups as areas where inspectors must demonstrate adequate
knowledge and skills.
(Response) AMS expanded the list of qualifications in the
rulemaking to include mass-balance audits and traceability audits.
These additions support changes to the USDA organic regulations for
supply chain traceability and on-site inspections as a result of this
rulemaking. DMI calculations, biosecurity, and internal control systems
for producer groups are specific to particular types of operations, and
AMS is not mandating these topics for general organic inspector
qualifications. Although knowledge of recordkeeping is not explicitly
included, some certifying agent personnel may need this knowledge if it
pertains to their duties (e.g., personnel who conduct supply chain
traceability audits).
(Comment) Comments recommended requiring special qualifications or
experience for inspectors who inspect high-risk operations, including
special training requirements for producer group operations.
(Response) AMS is not including special training requirements for
inspectors of high-risk operations or producer group operations.
Section 205.501(a)(4)(i) requires certifying agents to demonstrate that
their inspectors are qualified to inspect the operations of the scope
and complexity assigned. If an inspector is to inspect high-risk
operations or producer groups, then they must be qualified to inspect
those types of operations.
(Comment) Comments recommended clarifying that import/export skills
are needed only if relevant, as not all certifying agents deal with
import or export of organic products.
(Response) AMS is keeping import/export requirements in the
knowledge
[[Page 3583]]
areas required for all inspectors. Because this rule requires an NOP
Import Certificate for each organic shipment imported to the United
States, all inspectors must have knowledge of import and/or export
requirements and how they are implemented. Inspectors who regularly
inspect importing or exporting operations, or operations adjacent in
the supply chain, may require more advanced import/export expertise.
Training Requirements
(Comment) Some comments stated that an annual training requirement
violates labor laws regarding contractors. Commenters claimed
certifying agents cannot provide the training to contract inspectors,
so these inspectors will need to pay for the training, which could lead
to higher inspection fees.
(Response) All inspectors must meet the hourly annual requirements
for training that is relevant to their inspection work. While
certifying agents cannot require inspectors to complete trainings,
certifying agents must ensure all contract inspectors they use meet the
training requirement. The rulemaking adds clarifying detail to existing
training requirements to ensure consistent implementation by certifying
agents. In addition, there are various trainings available for free,
such as the online Organic Integrity Learning Center, which offers 33
courses averaging 3-4 hours per course. Additional no-cost resources
that could qualify for training include resources published by
universities, the USDA, or other organic experts (e.g., plant
identification databases, university extension courses, recorded
lectures, informational web pages) and organic farming conferences.
Furthermore, certifying agents commonly offer no-cost activities that
can count as training, such as updates to inspection procedure,
overviews of changes in organic regulation, supervised inspections, or
field visits. Because of the wide availability of no-cost training, and
because the rule's hourly training requirement is consistent with what
the industry already practices, AMS does not believe this requirement
will result in additional costs for inspectors beyond what is accounted
for the in the rule's economic analysis, or affect the cost of
inspection.
(Comment) Comments stated that the number of required training
hours should depend on how many different types of operations are
inspected by a particular inspector.
(Response) AMS revised the training hour requirements in the
rulemaking based on the types of operations inspected--see Sec.
205.501(a)(4)(i)(B) and (a)(4)(ii)(B).
(Comment) Comments showed concern that a specific numerical
training requirement is not appropriate. They stated that the required
content in the training is critical, not the number of training hours.
(Response) The annual training minimum is required to ensure the
regulation's specified knowledge, skills, and experience requirements
are effectively implemented. Establishing a minimum number of training
hours sets a clear baseline for inspector and certification reviewer
knowledge that promotes consistent implementation of the regulation by
certifying agents.
Experience Requirements
(Comment) Comments opposed the requirement that inspectors have one
year of field-based experience, asserting it was difficult to interpret
and may limit the pool of potential inspectors.
(Response) AMS agrees that the proposed use of ``field-based''
experience may be interpreted narrowly (e.g., only farming and organic
inspection experience) and that this may limit the pool of potential
new organic inspectors. The final rule is updated to reference
``relevant'' rather than ``field-based'' experience. This change
supports the use of a broader pool of qualified candidates, such as
persons with auditing or food handling experience.
(Comment) Comments recommended changing the proposed requirement
for one year of experience to a specific number of hours of related
experience.
(Response) AMS incorporated this recommendation into the final
rule. Inspectors are required to have at least 2,000 hours of relevant
experience prior to conducting their first inspection. This is
equivalent to one year of full-time work, and can be obtained across
multiple years, from one or more jobs, internships, or other qualifying
activities. This clarifies the requirement and expands the pool of
qualifying experiences across an individual's career and education.
(Comment) Comments recommended AMS adopt a ``mentoring and
evaluation system'' for inspectors in lieu of a one-year field-based
experience requirement because the proposed requirement was vague.
Comments stated requiring experience based on scope and scale was seen
as overly prescriptive and would limit the pool of qualified
inspectors.
(Response) The rulemaking does not codify an inspector mentoring
program. However, a mentorship program may be used by a certifying
agent to improve the quality and proficiency of their inspectors.
Mentorships may also count towards the 2,000-hour minimum experience
requirement, provided that the certifying agent can demonstrate that
the mentorship provided experience relevant to inspection.
Field Evaluation of Inspectors/Witness Inspections
(Comment) Several comments recommended that witness inspections
occur more frequently than once every three years, or that NOP issue
guidance for how to determine when witness inspections should be more
frequent.
(Response) Certifying agents may conduct witness audits more
frequently than once every three years ``if warranted.'' However,
certifying agents must also maintain documented policies, procedures,
and records for annual performance evaluations and witness inspections
(Sec. 205.501(a)(6)). This means that a certifying agent may choose to
conduct witness inspections more frequently than required by the
regulation (e.g., to monitor inspectors with performance issues), but
that the reason for more frequent witness audits should be justified
and documented in the certifying agent's policies and procedures.
Additionally, AMS increased the frequency of witness inspections
for inspectors with less than three years of experience from once per
three years to annually. This change was made to ensure that the
performance of new inspectors is consistently monitored and evaluated
by certifying agents.
(Comment) Comments recommended allowing virtual or remote witness
inspections.
(Response) Virtual and/or remote witness inspections were not
included in the SOE proposed rule and AMS is therefore not setting
specific policy related to virtual or remote witness inspections. The
final regulations provide flexibility so that AMS may consider virtual
witness inspection policy options in the future.
(Comment) Comments recommend allowing certifying agents to share
inspector evaluation reports with other certifying agents following
witness inspections.
(Response) AMS has addressed this recommendation in the rulemaking.
Certifying agents may share witness inspections reports with each
other. However, certifying agents using an inspector performance
evaluation or witness inspection report from another certifying must
demonstrate that they have evaluated the inspector's performance in
accordance with their
[[Page 3584]]
own internal personnel policies and procedures.
(Comment) Several comments expressed concern that the proposed
language would not allow contractors of a certifying agent to perform
witness inspections.
(Response) Certifying agents may use contractors to perform witness
inspections. However, the contracted personnel performing the witness
inspection must be qualified to evaluate the inspector (Sec.
205.501(a)(6)(i)).
(Comment) One comment stated that new inspectors should be shadowed
on 10 inspections during their first year, in addition to the proposed
20-hour training requirement.
(Response) AMS has not included this recommendation in the
rulemaking. Witness inspections will assess inspectors as they perform
their duties, with more frequent witness inspections of less
experienced inspectors. Comments did not demonstrate the benefit of
shadowing, although certifying agents may use this method if it is
documented in their policies and procedures for witness inspections.
I. Oversight of Certification Activities
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definition for Certification activity and Certification
office.
205.501............................................. General requirements for accreditation.
Paragraph (a)(22).
205.665............................................. Noncompliance procedure for certifying agents.
Paragraph (a).
----------------------------------------------------------------------------------------------------------------
This rulemaking revises the USDA organic regulations at Sec. Sec.
205.2, 205.501(a)(22) and 205.665(a) to clarify AMS's authority to
oversee the activities of certifying agents. Certifying agents must
notify AMS when opening any certification office that conducts
certification activities. In addition, this rulemaking clarifies that
AMS may issue notices of noncompliance to certifying agents based on
the certification activities of a party working on behalf of a
certifying agent.
Certifying agents, applicants for accreditation, and certified
operations may be affected by these requirements. Readers should
carefully review the regulations and policy discussion to determine if
they may be affected by this action.
Background
Certifying agents commonly have multiple offices to ensure they
provide adequate services to their clients. However, certifying agents
sometimes open new certification offices without reporting this to AMS.
Some certification offices operate independently and in different
countries or regions than a certifying agent's main office. AMS cannot
provide oversight (regular audits and reviews) or enforcement of
offices of which it is not aware. This can lead to inconsistent
application and enforcement of the regulations across certifying
agents. To address these gaps in oversight, the 2018 Farm Bill amended
OFPA to require certifying agents to report new certification offices
to AMS within 90 days of opening.\40\
---------------------------------------------------------------------------
\40\ See section 10104(d) of the Agriculture Improvement Act of
2018, Public Law No: 115-334, available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf (7 U.S.C.
6515(j)).
---------------------------------------------------------------------------
AMS also needs clear authority to initiate enforcement against
parties acting on behalf of a certifying agent (e.g., a subcontractor)
or individual certification offices. The use of subcontractors is
common in the organic industry and effective enforcement depends on
oversight of all persons involved in the certification of organic
operations. Uncertainty about whether AMS can target a certification
office or contractor for enforcement action interferes with precise and
expedited enforcement. Therefore, AMS revised the organic regulations
to clarify that entities acting on behalf of a certifying agent are
subject to oversight and enforcement.
90-Day Notification of New Certification Offices
To support the consistent application of the organic regulations
across all certifying agents, Sec. 205.501(a)(22) requires certifying
agents to notify AMS within 90 calendar days of the opening of any
office performing certification activities. A certification office is
defined as any site or facility where certification activities take
place, except for activities that take place at certified operations or
other specialized facilities, such as inspection, sampling, and
testing. This notification requirement applies to any facility or
location that meets the definition of certification office, regardless
of how the office is classified by a certifying agent (e.g.,
``central'' vs. ``satellite'' offices).
Notification of a new office opening must include basic information
to support effective oversight of the certification office, including
the countries serviced, location and nature of the certification
activities, and the qualifications of the personnel that will provide
the certification activities. Information on the location of new
offices allows AMS to efficiently use personnel and travel resources to
schedule on-site audits, and to be precise in any adverse action that
may affect only a portion of certifying agent's accreditation, e.g., a
certification office or activities in a specific country or region.
Information on the types of certification activities being conducted
allows AMS to better evaluate the need for additional oversight; for
instance, a new office located in a high-risk area with a history of
organic fraud may require additional oversight.
Authority To Issue Notices of Noncompliance
AMS is clarifying its authority to issue notices of noncompliance
to certifying agents based on the activities of persons acting on
behalf of a certifying agent, the activities of a certification office,
or the activities in a specific country. AMS added the term
certification activity to Sec. 205.2 of the organic regulations to
define activities that are essential to the function of a certifying
agent and therefore subject to NOP oversight. Certification activity is
any business conducted by a certifying agent, or by a person acting on
behalf of a certifying agent (e.g., a specific office operating in
specific countries, or a subcontractor or subcontractor organization).
Any business activity conducted by a certifying agent as it implements
the USDA organic regulations is considered a certification activity,
including review, inspection, and certification of organic operations.
The definition includes a non-exhaustive list of certification
activities that fall under AMS oversight authority.
[[Page 3585]]
AMS's authority to initiate enforcement action for a portion of a
certifying agent's operation is reinforced in Sec. 205.665(a)(1). This
states that AMS may send notifications of noncompliance to a certifying
agent based upon review of the certification activities of:
A person acting on behalf of the certifying agent or
A certification office.
This means that AMS may issue notices of noncompliance to a
certifying agent based on the activity of certifying agent
subcontractors, or an individual certification office(s) that may be in
a different location from the certifying agent's main office. Further,
AMS may suspend or revoke a portion of accreditation for activities in
a specific certification office, country, or region.
Summary of Changes to the Final Rule
AMS made no changes to the proposed regulatory text in Sec. Sec.
205.2, 205.501(a)(22), and 205.665(a) with respect to oversight of
certification activities and has finalized the proposed requirements.
Summary of Public Comment
The majority of public comments supported AMS's proposed
clarification. Commenters were primarily concerned that the proposed
definition of certification office would subject remote staff and home
offices to NOP audits. Commenters stated that NOP audits of home
offices and remote workers does not align with NOP's intent for adding
the term certification office. Comments suggested excluding home
offices and telework locations from the definition for certification
office, and some explained that certifying offices which solely operate
virtually should qualify as a certification office and individual
workers working remotely on a temporary basis should not be subject to
NOP audits.
Commenters were also concerned that the 90-day timeframe for
certifying agents to notify AMS of new offices conducting certification
activities is too long.
Responses to Public Comment
Definition of Certification Office
(Comment) AMS received comments requesting that the definition of
certification office exclude home offices and remote workers.
Commenters asserted that if home offices for remote staff are included
in the definition of certification offices, they will be subject to
audits, which would be unreasonable.
(Response) Home offices are not excluded in the definition of
certification office because some certifying agents may maintain home
offices as their primary location or certification office from which
they conduct certification activities.
90-Day Notification of New Offices
(Comment) We received comments stating that the 90-day timeframe
for certifying agents to notify AMS of new offices conducting
certification activities is too long. Some suggested that timeframes of
30 or 45 days would be more appropriate.
(Response) The 2018 Farm Bill established the 90-day timeframe.
Section 10104 (j) of the 2018 Farm Bill and 7 U.S.C. 6515(j) state
``Not later than 90 days after the date on which a new certifying
office performing certification activities opens, an accredited
certifying agent shall notify the Secretary of the opening.'' While
certifying agents may choose to notify AMS earlier, AMS is retaining
the 90-day notification requirement in the organic regulations.
(Comment) Commenters asked what office types (e.g., satellite
offices or main offices) would require a certifying agent to notify
AMS.
(Response) Certifying agents must notify AMS of the opening of any
type of office where certification activities take place. This
requirement for notification is based on the activities of an office
not the type.
J. Accepting Foreign Conformity Assessment Systems
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definitions for Conformity assessment system and Technical
requirements.
205.511............................................. Accepting foreign conformity assessment systems.
Entire section.
----------------------------------------------------------------------------------------------------------------
AMS has added a new section to the USDA organic regulations, Sec.
205.511, on accepting foreign conformity assessment systems that
oversee organic certification in foreign countries. Section 205.511
replaces former Sec. 205.500(c).
Affected entities may include, but are not limited to:
Trade partners who have established an organic equivalence
determination or are interested in establishing an equivalence
determination with the United States.
Foreign certifying agents and certified operations not
accredited or certified by the USDA.
Foreign organic producers who export products to the
United States.
The above list is a general description of entities likely to be
affected by this action. Other types of entities could also be
affected. You should carefully examine the regulatory text to determine
if you or your organization may be affected by this action.
Background
The OFPA, under 7 U.S.C. 6505(b), allows imported organic products
to be sold or labeled in the United States as organically produced if
the Secretary determines that the products have been produced and
handled under an organic certification program with requirements and
oversight determined to be at least equivalent to those described in
the OFPA. Under this authority, the U.S. government, including the USDA
and the U.S. Trade Representative, work closely together to implement
processes that determine the equivalence of foreign organic
certification programs and then negotiate an arrangement or agreement
as appropriate.
USDA organic regulations formerly addressed USDA's authority to
make equivalence determinations in general terms under Sec.
205.500(c), but did not describe the criteria, scope, and other
parameters to establish, oversee, or terminate such equivalence
determinations, which are critical to the enforcement of organic
imports. This new Sec. 205.511 does not change current policy or add
any new requirements. It codifies existing practices and clarifies the
procedures followed when determining organic equivalence, which
strengthens oversight and enforcement capacity of organic imports by
supporting the government's authority to reassess, continue, and
terminate equivalence determinations, as
[[Page 3586]]
necessary. Without this clear implementation of Federal authority in
the USDA organic regulations, the government could face challenges
establishing and enforcing terms under current and future equivalence
determinations that are critical to ensuring the integrity of imported
organic products.
Definitions
The rulemaking adds two new terms in Sec. 205.2: conformity
assessment system and technical requirements. These terms are defined
to ensure that the process and requirements described in Sec. 205.511
are clear. The rulemaking defines conformity assessment system as all
activities, including oversight, accreditation, compliance review, and
enforcement, undertaken by a government to ensure that the applicable
technical requirements for the production and handling of organic
agricultural products are fully and consistently applied. The
rulemaking defines technical requirements as a system of relevant laws,
regulations, regulatory practices, standards, policies, and procedures
that address the certification, production, and handling of organic
agricultural products.
Foreign Product Certification
Section 205.511(a) describes the U.S. government's authority under
OFPA to make equivalence determinations and explains the conditions in
which foreign-produced product can be labeled and sold as organic in
the United States.
Equivalency Determination Request
Section 205.511(b) describes the process used by the U.S.
government and other foreign governments for initiating a request for
an equivalence determination. Since there are several factors that may
impact whether the U.S. government moves forward to review an
equivalence determination request (e.g., agency resources, capacity to
oversee the potential trade arrangement or agreement, relative benefits
for the U.S. organic sector), this section clarifies that the U.S.
government will determine if it can proceed with the evaluation process
on a case-by-case basis.
Equivalency Reviews and Reassessments
Section 205.511(d) lays out the current process that AMS and other
foreign governments use to monitor equivalence determinations that have
been made. The section provides some flexibility in the timing of
reviews to accommodate unavoidable factors in both countries that can
impact timing (e.g., federal budgets, election cycles, growing
seasons).
Equivalence Termination Procedures
Section 205.511(e) describes the conditions under which the U.S.
government may terminate equivalence determinations. These conditions
for termination are commonly accepted among countries that maintain
equivalence determinations and are based upon the core concepts
underlying equivalence. The U.S. government must be able to terminate
equivalence determinations under these conditions in order to fulfill
its statutory obligation to assure that organic products sold in the
United States are compliant with OFPA and the USDA organic regulations
and maintain a level playing field for U.S. farms and businesses.
In addition to the conditions described in Sec. 205.511(e), the
U.S. government may also terminate an equivalence determination ``for
other good cause.'' This includes risks that may negatively affect the
integrity of organic products imported from a country with which the
U.S. government has an equivalence determination, policy changes, or
resource constraints that impact either government. Examples include:
Repeated cases of organic fraud that are not corrected by
a foreign government;
Increasing levels of organic fraud that a foreign
government is unable or unwilling to address;
Political instability, safety concerns, or limitations on
access that make it impossible for USDA to travel to and assess a
foreign government's equivalence determination;
Reduction in funding or other resources that compromises a
foreign government's or USDA's ability to operate its organic program
and oversee the equivalence determination; or
Changes in a foreign government's unilateral equivalence
determination with the USDA that may restrict domestic producers'
access to foreign markets.
In all cases, the U.S. government would provide notice and
justification to the foreign government prior to termination, and give
notice to affected organic stakeholders along with a reasonable
timeline to transition.
Summary of Changes to the Final Rule
AMS made several revisions to the proposed regulatory text when
writing this final rule. Changes to the proposed rule are discussed
below and are followed by responses to specific themes from public
comment.
AMS added ``oversight, accreditation, compliance review,
and enforcement'' to the definition of conformity assessment system to
clarify the scope of the assessment of a foreign organic certification
system's eligibility for an equivalence determination.
AMS added ``standards, policies'' and ``certification'' to
the definition of technical requirements to clarify the scope of this
term and to ensure that the definition covers all parts of a country's
framework for regulating organic products.
AMS corrected the syntax of Sec. 205.511(a) and (b) to
state that foreign product ``may be sold, labeled, or represented in
the United States as organically produced.'' This accurately reflects
the intent to allow foreign organic product to be exported to the
United States and sold as organic, but does not allow foreign organic
product to be labeled as domestically produced in the United States.
AMS removed the reference to a two-year review cycle in
Sec. 205.511(d) and replaced with a statement explaining how AMS will
determine the timing and scope of reviews of equivalence
determinations. This gives AMS the flexibility to determine timelines
for audits and reassessments of equivalence determinations, and allows
AMS to accommodate unavoidable factors when scheduling audits and
reassessments of equivalence determinations.
Summary of Public Comment
Public comments showed overall support for codifying AMS's existing
practices for determining organic equivalence, agreeing that the
proposed updates would strengthen the integrity of imported organic
products.
Several of these comments largely focused on how the specifics of
the proposed Sec. 205.511 would improve the transparency and oversight
of equivalence determinations and recognition agreements. Some of these
comments recommended requiring certified foreign operations to be
listed in the Organic Integrity Database and for NOP to investigate any
countries with equivalence determinations found to be noncompliant.
Some comments expressed opinions in opposition to some existing trade
arrangements, and/or suggested that USDA not allow equivalence
determinations and require direct certification via USDA-accredited
certifying agents instead. Some comments were also uncertain the
proposed requirements of Sec. 205.511 apply to recognition agreements.
Several comments expressed concern that the proposed Sec.
205.511(a) and (b)
[[Page 3587]]
would allow organic products produced under foreign equivalence
determinations to be sold as ``produced in the United States.'' Some
comments pointed out that the two and five-year inspection timelines
may conflict with other regulations.
Responses to Public Comment
Definition of Conformity Assessment Systems
(Comment) AMS received comments requesting that several activities
be included in the definition of conformity assessment systems.
Commenters stated that it is critical to ensure that foreign
governments have sufficient oversight, accreditation, compliance, and
enforcement mechanisms in place to ensure that organic technical
requirements are being enforced.
(Response) The definition of conformity assessment systems has been
modified from the proposed rule to include the following activities:
oversight, accreditation, compliance review, and enforcement. The
additional activities were added to the definition of conformity
assessment systems to clarify the scope of the assessment of a foreign
organic certification system's eligibility for an equivalence
determination.
Definition of Technical Requirements
(Comment) We received comments requesting that the definition of
technical requirements include the terms standards, policies, and
certification. Commenters stated that it was important that these terms
be added to ensure that the definition covers all parts of a country's
framework for regulating organic products.
(Response) The terms standards, policies, and certification have
been added to the definition of technical requirements. The new terms
were added to ensure that the definition covers all parts of a
country's framework for regulating organic products.
Labeling of Foreign Product Origin
(Comment) Comments noted that Sec. 205.511(a) could be interpreted
to allow labeling of foreign-produced organic product as ``produced in
the United States.''
(Response) The final rule corrects the syntax of Sec. 205.511(a)
to state foreign organic product ``. . . may be sold, labeled, or
represented in the United States as organically produced.'' This
accurately reflects the intent to allow foreign organic product to be
exported to the United States and sold as organic, but does not allow
foreign organic product to be labeled as domestically produced in the
United States.
Equivalence Reviews and Reassessments
(Comment) We received comments requesting AMS clarify its timeline
for audits and reassessments of equivalence determinations.
Additionally, commenters noted the difference between proposed Sec.
205.511(d), which requires a two-year midcycle review, and the proposed
rule preamble, which states, ``The review cycles mirror ISO standards,
which include a five-year reassessment cycle and mid-cycle reviews.''
(Response) The final rule has been revised to allow AMS additional
flexibility to determine timelines for audits and reassessments of
equivalence determinations. The final rule replaces ``two-year cycle''
and ``five years'' with the phrase ``regular reviews and
reassessments.'' The new regulatory language allows AMS to accommodate
unavoidable factors when scheduling audits and reassessments of
equivalence determinations.
(Comment) AMS received comments asking if recognition agreements
would be subject to AMS audits and reassessments per new Sec. 205.511.
(Response) Recognition agreements will be subject to AMS audits and
reassessments of equivalence per Sec. 205.511.
Equivalence Determination Procedures
(Comment) We received comments requesting AMS describe in Sec.
205.511(e) the criteria used to determine termination of an equivalence
determination.
(Response) Each equivalence determination is unique and is assessed
using the general criteria described in Sec. 205.511. To ensure fair
assessment of each unique equivalence determination, AMS has not
codified specific criteria used to determine termination of
equivalence.
K. Compliance and Noncompliance Procedures
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.660............................................. General.
Paragraph (c).
205.661............................................. Investigation.
Change section heading only.
205.100............................................. What has to be certified.
Paragraph (c).
205.662............................................. Noncompliance procedure for certified operations.
Paragraphs (e)(3), (f)(1), and (g)(1).
----------------------------------------------------------------------------------------------------------------
Authority To Pursue Enforcement Action Against Any OFPA Violator
The NOP currently pursues enforcement actions against uncertified
parties when AMS has evidence of OFPA violations. In 2021, more than
half of the complaints received by the NOP alleging violations of OFPA
involved uncertified operations representing products as organic.
Continued AMS enforcement against uncertified operations is central to
the effective administration of the OFPA.
The rulemaking updates the USDA organic regulations by adding new
paragraph (c) to Sec. 205.660, to clarify that the NOP Program Manager
may initiate an enforcement action against any violator of OFPA,
regardless of certification status. Consistent with the new paragraph
(c) to Sec. 205.660, to clarify that the NOP Program Manager may
initiate an enforcement action against any violator of the OFPA, AMS
changed the title of Sec. 205.661 from ``Investigation of Certified
Operations'' to ``Investigation.''
Enforcement Action Against Responsibly Connected Persons
Person(s) responsibly connected to a violator of the OFPA may be
complicit in the OFPA violation(s) because of their association to the
violator. Because of this, the rulemaking clarifies at Sec. Sec.
205.100 and 205.662 that any person who is responsibly connected to an
operation that violates OFPA or the USDA organic regulations may be
subject to a suspension of certification, civil penalties, or criminal
charges and/
[[Page 3588]]
or may be ineligible to receive certification. This clarification
strengthens AMS's enforcement capacity by ensuring that enforcement
actions and penalties for violations of the OFPA extend to all
accountable parties.
Responsibly connected persons who are suspended or revoked may
request to have their certification reinstated, if suspended, or their
eligibility to become certified reinstated, if revoked. AMS has
published guidance for Reinstating Suspended Operations (NOP 2605),
which applies to both suspended and revoked operations that want to
become certified again.\41\
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\41\ Instruction NOP 2605, Reinstating Suspended Operations:
https://www.ams.usda.gov/sites/default/files/media/2605.pdf.
---------------------------------------------------------------------------
Timely Updates to the Organic Integrity Database
Timely updates to the Organic Integrity Database (OID) are critical
to inform other certifying agents, operations in the supply chain, and
consumers when an operation is no longer certified and can help prevent
noncompliant products from entering or continuing in the stream of
commerce. At Sec. 205.662(e)(3) of the regulations, AMS requires
certifying agents to provide timely updates on the status of an
operation that has been suspended or revoked (or that has surrendered
its organic certification). These updates should be viewable in the
Organic Integrity Database within three business days of issuing a
notification of suspension or revocation, or from the effective date of
a surrender. This publicly available information helps businesses in
the supply chain confirm that an operation from which they purchase or
receive organic products has a valid organic certification.
In most cases, the effective date of an operation's surrender means
that the certifying agent has received notification from the operation
and confirmed the surrender status. AMS recognizes that in some cases
the effective date of the surrender may date prior to certifying agent
confirmation of surrender and the Organic Integrity database updates
will extend past the three-day window.
Federal Civil Penalty Inflation Adjustment
Finally, AMS amended Sec. 205.662(g)(1) of the regulations to
update the citation which specifies the maximum civil penalty amount
for violations of the OFPA. Title 7 CFR 3.91(b)(1)(xxxvi) provides the
civil penalty amount for each violation of OFPA. This amendment aligns
with the Federal Civil Penalties Inflation Adjustment Act Improvements
Act of 2015, Public Law 114-74, sec. 701.\42\
---------------------------------------------------------------------------
\42\ https://www.govinfo.gov/content/pkg/PLAW-114publ74/html/PLAW-114publ74.htm. As of the publication of this rule the civil
penalty amount is $20,130 per violation of OFPA occurring on or
after February 15, 2022. The civil penalty amount will be adjusted
in the future so readers should refer to 7 CFR 3.91(b)(1)(xxxvi) for
the current amount.
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Changes From Proposed to Final Rule
AMS made one change to the proposed regulatory text when writing
this final rule:
Removed the phrase ``directly or indirectly'' from
205.660(c) because its meaning was confusing. The intent of 205.660(c)
is to clarify the scope of potential enforcement actions which may
include blatant and subtle false labeling and representation of
nonorganic products as organic.
No other changes were made to the proposed regulatory text in
Sec. Sec. 205.100(c), 205.660(c), 205.662(e)(3)), and 205.662(f)(1)
and AMS has finalized the proposed requirements with respect to AMS's
authority to enforce against any OFPA violator and all responsibly
connected persons connected to a violator. AMS also made no changes to
proposed requirement to timely update the Organic Integrity Database.
Summary of Public Comments
In general, most public comments supported the proposed revisions
to clarify AMS's authority to enforce against any violator of the OFPA
and the organic regulations. Many comments also discussed the revisions
in detail and offered recommendations or changes to the proposed
policy.
Many comments discussed the proposed three-day timeframe to submit
updates to the Organic Integrity Database (Sec. 205.662(e)(3)). Some
comments describe the requirement as too burdensome, while some support
the three-day timeframe. Comments opposing the proposed requirement
recommended alternatives ranging from 7 to 30 days. Other comments
state that updates should be immediate, or made within 48 hours, so
that noncompliant products do not continue in the stream of commerce.
Several comments also claim that identifying and tracking all
responsibly connected persons would be difficult, and requested more
guidance on how this should be done. A few comments asked AMS if
revocation of an operation's certification should also result in the
revocation of all responsibly connected persons' certification.
Some comments also asked AMS to clarify the phrase ``or submit a
request for eligibility to be certified'' in Sec. 205.662(f)(1). A few
comments also asked if this applies to persons responsibly connected to
a suspended operation. One comment also asked if this section applies
to revocation of certification.
Responses to Public Comment
Timely Updates to the Organic Integrity Database
(Comment) AMS received comments that the three-day requirement to
update the Organic Integrity Database is too burdensome. Commenters did
not quantify negative impacts to certifying agents, nor did they
clearly explain why this would be burdensome for certifying agents.
Others supported the three-day timeframe or recommended that updates
should be immediate or within 48 hours, so that noncompliant products
do not continue in the stream of commerce. Other commenters recommended
alternatives ranging from 7 to 30 days.
(Response) Certifying agents will have a one-year implementation
period before this requirement takes effect. During the implementation
period, there is no fixed time frame for updating data in the Organic
Integrity Database. This requirement is limited in scope and applies
when an operation is suspended, revoked, or has surrendered organic
certification. Public accessibility of an operation's correct
certification status is essential for movement of products in organic
supply chains. AMS believes that three days for certification status
updates is adequate and supports organic verification across supply
chains of different speeds. Extending the deadline beyond three days
may interfere with the timely verification of an operation's accurate
certification status. This is critical data and inaccurate information
can delay legitimate transactions and fail to prevent sales of products
from suspended or revoked operations. Further, AMS provides certifying
agents with an API to upload data to the Organic Integrity Database,
which reduces redundant or duplicative work for certifying agents.
Enforcing Against Responsibly Connected Persons
(Comment) AMS received comments stating that identifying and
tracking all responsibly connected persons would be difficult because
these entities are not listed in the Organic Integrity
[[Page 3589]]
Database. Commenters requested guidance on how this should be
accomplished.
(Response) AMS is not specifying how certifying agents must
identify responsibly connected persons, nor are we requiring
responsibly connected persons to be listed and searchable as such in
the Organic Integrity Database. Obtaining responsibly connected persons
from organic system plans and/or identifying all known responsibly
connected persons in adverse action letters are best practices that
certifying agents should pursue.
Use of Term ``Indirectly'' in 205.660(c)
(Comment) Commenters requested clarification of what is meant by a
label or information which ``indirectly'' implies that product was
produced with organic methods if product was produced in violation of
the OFPA or the organic regulations.
(Response) AMS removed the phrase ``directly or indirectly'' from
205.660(c) because its meaning was confusing. The intent of 205.660(c)
is to clarify the scope of potential enforcement actions which may
include blatant and subtle false labeling and representation of
nonorganic products as organic.
Civil Penalty Citation
(Comment) For civil penalty fines, commenters requested AMS cite
the regulation, not the amount, since the latter changes and becomes
outdated.
(Response) The proposed and final rules cite the regulation that
sets the civil penalty amount.
Documented Delivery Confirmation
(Comment) Commenters requested AMS allow ``documented delivery
confirmation'' to accommodate electronic communication rather than only
certified paper mail.
(Response) AMS accepts that ``dated return receipts,'' which are
required when certifying agents or NOP sends an adverse action notice
to an operation, may include electronic communications. This means that
the adverse action notices may be sent electronically to the recipient
and delivery confirmation may include, for example, confirmation that
an email has been delivered.
L. Mediation
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.504............................................. Evidence of expertise and ability.
Introductory text and paragraph (b)(8).
205.663............................................. Mediation.
Entire section.
----------------------------------------------------------------------------------------------------------------
Background
AMS revised Sec. 205.663 to improve the general readability of
this section and to more clearly explain how mediation may be used in
noncompliance procedures. When successful, mediation is an efficient
way to bring operations into compliance and resolve conflicts among
certifying agents and operations. The USDA organic regulations require
that certifying agents and State organic programs provide applicants
for certification and certified operations the right to request
mediation when they issue a denial of certification, notice of proposed
suspension, or proposed revocation of certification (Sec. Sec.
205.405(d) and 205.662(c)). Section 205.663 provides requirements for
requesting mediation, responding to a mediation request, the time frame
for reaching an agreement, and what happens when mediation is
unsuccessful.
The USDA organic regulations require certifying agents and State
organic programs to notify operations of the option to request
mediation as an alternative dispute resolution to resolve noncompliance
findings that have led to a proposed suspension, revocation, or denial
of certification. This will facilitate resolution of these issues
before they escalate to an appeal to AMS or a State organic program.
Mediation Is a Collaborative Process
The requirements for mediation support a process that is efficient
and accessible to producers and handlers who want to resolve a denial
of certification, proposed suspension, or revocation of certification.
Mediation is a collaborative process between a certifying agent and an
operation or applicant for certification. A successful mediation
addresses the noncompliance(s) and leads to full compliance with the
USDA organic regulations. To ensure that mediation is readily
accessible, certifying agents and certified operations or applicants
may engage in mediation without a third-party mediator, provided that
all parties agree upon the person who will serve as the mediator.
Mediation Must Be Requested in Writing
After a certifying agent issues a denial of certification, proposed
suspension, or revocation of certification, a certified operation and
certifying agent may discuss the option of mediation prior to receiving
a request for mediation. However, for mediation to proceed as a form of
alternative dispute resolution, an operation must request mediation in
writing to the certifying agent. The request for mediation must be
submitted to the certifying agent within 30 calendar days from the date
of the proposed adverse action or denial of certification (Sec.
205.663(b)(1)). This aligns with the length of time provided to submit
an appeal of a proposed adverse action.
Mediation Acceptance Criteria
A certifying agent determines whether to accept or reject a written
request for mediation. Certifying agents must include mediation
acceptance decision criteria as part of the administrative policies and
procedures which certifying agents are required to submit to
demonstrate their ability to comply with the certification program
(Sec. 205.504(b)(8)). The mediation acceptance criteria must be fair
and reasonable and not arbitrary. The criteria must be based on factors
that will likely determine potential success or failure of the
mediation process. The certifying agent must document how it applied
the criteria to accept or reject requests for mediation. Parties to the
mediation may develop conditions, such as cost, timeframes to reach a
settlement agreement within the allowed maximum of 30 days, and any
incremental steps, only after a certifying agent accepts a mediation
request. A certifying agent must not impose any preconditions for the
acceptance of mediation (i.e., the certifying agent cannot require that
the operation take a specific action--other than submitting a written
request for mediation--before it will consider mediation).
[[Page 3590]]
If a certifying agent decides to reject a request for mediation,
based on its criteria for acceptance of mediation, it must inform the
operation in writing, with the justification for the rejection. That
notification must explain that the operation has the right to appeal
the rejection of mediation (Sec. 205.663(b)(3)). While an operation
appeals a rejection of mediation, the proposed suspension or revocation
which led to the request for mediation must not be finalized (Sec.
205.663(b)(4)). The date that the notification is received by the
operation is important because it starts the 30-day window for filing
an appeal and may be used to determine whether an appeal has been
timely filed. Likewise, when mediation is unsuccessful, the certifying
agent must inform the operation in writing to document the start of the
30-day window for filing an appeal. This means that certifying agents
must send rejection and termination of mediation notices using a method
with delivery confirmation.
Use of Settlement Agreements
In accepting mediation, a certifying agent may also, at its
discretion, offer a settlement agreement for an operation to consider
(Sec. 205.663(e)). The outcome of successful mediation is a settlement
agreement that brings an operation into compliance with the USDA
organic regulations. A settlement agreement must clearly describe the
corrective actions and timeframes for implementing corrective actions,
and may impose additional actions (e.g., unannounced inspections,
sampling for residue testing) to ensure the operation maintains
compliance. A settlement agreement may also include a suspension of
organic certification.
A settlement offer may be useful when the corrective action(s) is
clear and the noncompliance(s) is not recurrent. As part of the
mediation, an operation may accept or reject the settlement agreement,
negotiate the terms with the certifying agent, or request a mediator to
try and reach a settlement agreement.
Use of a Third-Party Mediator
This rule clarifies that mediation does not require a third-party
mediator to reach a settlement agreement (Sec. 205.663(c)). The
certifying agent and operation may agree that mediation will be between
only those two parties. For example, mediation may consist of a phone
call or series of phone calls between the operation and the certifying
agent to discuss the terms of a settlement offer prior to signing the
agreement.
In some cases, the use of a third-party mediator may be
appropriate, either because the operation initially requested this, or
the operation rejected a settlement offer and then requested a
mediator. To demonstrate their ability to comply with the certification
program, each certifying agent must submit a process to identify a
qualified mediator and set the time and location of mediation
session(s), mediation format (in-person, video, phone), and mediation
fees and payment (Sec. 205.504(b)(8)).
Role of the Program Manager
The Program Manager does not require, manage, or otherwise
participate in mediation between operations and certifying agents or
State organic programs. The Program Manager may review an agreement
that results from the mediation for conformity to the OFPA and the USDA
organic regulations and reject any nonconforming provision or agreement
(Sec. 205.663(f)). The Program Manager may direct the certifying agent
or State organic program to revise any nonconforming provisions, and
the operation would have a new opportunity to accept or reject the
revised settlement agreement.
Mediation under the USDA organic regulations is an alternative
dispute resolution mechanism, conducted between a certified operation
or applicant for certification and a certifying agent or State organic
program. The Program Manager is not involved in determining the outcome
of a mediation, notwithstanding his or her authority to review dispute
resolution terms for conformity with the OFPA and the USDA organic
regulations.
This does not affect AMS's ability to carry out oversight,
compliance, and enforcement activities on behalf of the Program
Manager. For example, AMS may conduct informal mediation, at its
discretion, and enter into mutually agreeable settlement agreements
with parties that receive a proposed adverse action (Sec. 205.663(g)).
Changes From Proposed to Final Rule
AMS made minor revisions to the proposed regulatory text when
writing this final rule. Changes to the final rule are discussed below
and are followed by specific themes from public comment.
AMS added the words ``of receipt'' to Sec. 205.663(b)(3)
and (e) so that the 30-day time frame for requesting an appeal when
mediation is rejected or terminated provides adequate due process and
aligns with the appeal filing time frame for other adverse action
notices.
AMS added a requirement for termination of mediation to be
documented in a written notice so it is clear when an operation may
exercise its right to file an appeal.
AMS revised the introductory paragraph at Sec. 205.504 to
include the cross-reference to Sec. 205.663 because certifying agents
must submit mediation procedures as part of the evidence of their
ability to comply with and implement mediation requirements.
AMS relocated the requirement to submit mediation policies
and procedures from Sec. 205.663(a) to Sec. 205.504(b), where
requirements for certifying agents' policies and procedures are
identified.
AMS added a requirement that certifiers document the
reason for denying mediation. If the rejection is appealed, this will
allow the Administrator to determine whether the rejection was
reasonable and consistent with the certifier's criteria for rejection.
AMS added the word ``reasonable'' to Sec. 205.504(b)(8)
to describe parameters for the criteria that certifiers must set for
accepting mediation. This supports fair and consistent decisions on
requests for mediation across certifying agents.
AMS revised Sec. 205.663(e) to require that a settlement
agreement be reached within 30 days from the start of mediation. This
clarifies when the 30-day timeframe begins and supports timely
resolution of compliance issues.
AMS added a new provision at Sec. 205.663(b)(4) to
clarify that an adverse action (e.g., proposed suspension or
revocation) must not be finalized during the appeal proceeding. This
clarification supports the right to adequate due process before an
adverse action takes effect.
Responses to Public Comment
Settlement Agreements
(Comment) Several commenters asked questions about the management
of settlement agreements.
(Response) AMS is not addressing questions about management of
settlement agreements in this rule because they are beyond the scope of
this rule. More information on settlement agreements is available
through the Organic Integrity Learning Center and annual training for
certifying agents.
Mediation
(Comment) AMS received a comment stating certifying agents should
be allowed to propose mediation and offer settlement agreements.
(Response) The regulations do not prohibit a certifying agent from
[[Page 3591]]
informing an operation of its willingness to engage in mediation prior
to an operation requesting mediation. In addition, the regulations do
not prohibit a certifying agent from offering a settlement agreement as
part of mediation to resolve an adverse action.
(Comment) AMS received a comment to replace the terms ``mediation
session'' with ``mediation'' to allow informal mediation at Sec.
205.663(e).
(Response) AMS replaced ``mediation session'' with ``mediation'' to
account for informal mediation which may not use the same format as
formal mediation.
(Comment) AMS received a comment to change the deadline to submit a
request for mediation from ``30 days from receipt'' to ``30 days from
date of issue.''
(Response) AMS is declining to make this change, in order to align
with USDA's Office of Administrative Hearings and Appeals, which uses
date of receipt and not date of issue. This practice preserves due
process rights of operations being notified of adverse actions. AMS
believes that the use of electronic communications and the availability
of electronic delivery confirmation will make this requirement less
burdensome.
(Comment) Comments requested that AMS align language for timeframes
for requesting mediation and requesting an appeal.
(Response) AMS agrees that the timeframes for requesting mediation
and requesting an appeal when mediation fails should be consistent. We
changed Sec. 205.663(b)(3) to state that an operation has 30 days from
receipt of the rejection of request for mediation to file an appeal. We
also changed Sec. 205.663(e) to state that an operation has 30 days
from receipt of a written notice of termination of mediation to file an
appeal. These changes make the timeframes to file an appeal consistent
whether mediation is rejected or terminated.
(Comment) AMS received a comment that both parties agreeing on the
person conducting mediation should only apply to formal mediation.
(Response) AMS disagrees that consensus on the person conducting
mediation should only apply for formal mediation. Informal mediation
also requires that parties agree on who will facilitate the mediation,
even when the parties to the mediation facilitate the process
themselves.
M. Adverse Action Appeal Process
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definition for Adverse action.
205.680............................................. Adverse Action Appeal Process--General.
Entire section.
205.68.............................................. Adverse Action Appeal Process--Appeals.
Paragraphs (a), (a)(2), (b), (c), and (d)(1) and (2).
----------------------------------------------------------------------------------------------------------------
General Appeals
AMS revised parts of the adverse action appeals process in
Sec. Sec. 205.680 and 205.681. These changes clarify which actions can
be appealed, recognize the use of alternative dispute resolution in
lieu of a formal administrative proceeding to resolve an appeal, and
reinforce that appeal submissions need to comply with the basic
requirements in the regulations.
The OFPA calls for an expedited appeals procedure that gives
persons affected by a proposed adverse action the opportunity to appeal
that action (7 U.S.C. 6520). All appealed adverse actions are
expeditiously reviewed and decided in an unbiased manner by persons
that are not involved in the initial decision to issue an adverse
action. In December 2014, AMS issued guidance to explain how it
administers the adverse action appeal process, the status of an
appellant during an appeal, and the possible outcomes of an appeal in
NOP 4011, Adverse Action Appeal Process.\43\
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\43\ NOP 4011, Adverse Action Appeal Process. December 23, 2011:
https://www.ams.usda.gov/sites/default/files/media/4011.pdf.
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The original USDA organic regulations described how certified
operations, accredited certifying agents, and applicants for
certification or accreditation may appeal a noncompliance decision that
would affect their certification or accreditation status or eligibility
to become certified or accredited (Sec. 205.680(a)). The regulations
explained when an appeal may be submitted, how it must be submitted,
and what the appeal submission must contain. Specifically, appeals of
noncompliance decisions of a certifying agent or NOP are appealable to
the AMS Administrator, or to the State organic program if the appellant
is in a State with an approved State organic program. A decision to
sustain an appeal will result in a favorable action with respect to the
appellant's certification or accreditation. Following a decision to
deny an appeal, AMS will initiate a formal administrative proceeding
(i.e., a hearing), unless the parties resolve the issue through
settlement, or the appellant waives the hearing. If an appeal is not
timely filed, the adverse action which led to the appeal will be final
and cannot be appealed further.
Adverse Action Defined
The new term adverse action clarifies which actions may be appealed
under the USDA organic regulations. Adverse action replaces the use of
``noncompliance decision'' throughout this section. Adverse action is
defined as a noncompliance decision that adversely affects
certification, accreditation, or a person subject to the Act, including
a proposed suspension or revocation; a denial of certification,
accreditation, or reinstatement; a cease-and-desist notice; or a civil
penalty.
Option To Request Mediation or Appeal of an Adverse Action Issued by a
Certifying Agent or State Organic Program
When a certifying agent or State organic program issues a proposed
suspension or revocation, operations have the option to request
mediation or appeal the proposed adverse action. Mediation is covered
in more detail in Sec. 205.663. The mediation process can be a viable
path to resolve noncompliances that are correctable and are not willful
or recurrent. If mediation is rejected or is not successful, the
operation maintains the right to appeal. The time frame for filing an
appeal is calculated from receipt of the notice of rejection or
termination of mediation (Sec. 205.663(b)(3) and (e)).
Administrative Requirements
Appeals must be properly filed as described in paragraphs (c) and
(d) of Sec. 205.681. This means that an appeal must be:
[[Page 3592]]
Filed in writing within the time period provided in the
letter of notification or within 30 days from receipt of the
notification, whichever occurs later.
Sent to the correct physical or email address:
[cir] 1400 Independence Ave. SW, Room 2642, Stop 0268, Washington,
DC 20250.
[cir] [email protected].
Include a copy of the adverse action and explain why the
adverse action is incorrect.
An adverse action will become final and nonappealable unless an
appeal is timely filed. Appeals will be considered ``filed'' on the
date received by the Administrator or by the State organic program.
Denied Appeals
AMS supports the use of alternative means, such as mediation and
settlement agreements to expedite resolution of an adverse action
dispute while preserving due process and avoiding prolonged formal
proceedings. When an appeal is denied, AMS offers the appellant the
option to waive further hearing. When an appellant waives a hearing,
the appeal decision is final and takes effect. Failing to timely submit
a request for hearing is regarded as a waiver of hearing. In some
cases, when an appeal is denied, AMS may pursue a settlement agreement
in lieu of initiating a formal administrative proceeding. AMS assesses
the potential for a settlement agreement on a case-by-case basis and
will exercise this option when a settlement may offer a viable route
for the operation to come back into compliance or to exit the organic
sector. Even when an appellant requests a hearing, AMS and the
appellant may enter into a settlement agreement prior to the hearing.
This provides flexibility to resolve appeals outside of a lengthy
formal administrative process. The appellant reserves the right to an
administrative hearing. Entering into a settlement agreement is an
optional, not compulsory, alternative to a hearing.
Changes From Proposed to Final Rule
AMS made several revisions to the proposed regulatory text when
writing this final rule, including revising Sec. 205.681(a)(2) and
(b)(2) to state that the Administrator will initiate a formal
proceeding and identify the conditions when that would not occur, i.e.,
the parties settle beforehand, or the appellant waives its right to a
hearing. These sections explain that failing to timely request a
hearing constitutes a waiver of hearing. AMS also deleted ``policies
and procedures'' from 205.681(d)(3) to clarify that the USDA organic
regulations are the basis for enforcement.
Summary of Public Comments
Comments were generally supportive of the clarifications to the
appeals sections of the USDA organic regulations. The main concern in
comments was the revision to state that AMS ``may'' rather than
``will'' initiate a formal administrative proceeding if the
Administrator denies an appeal. The comments stated that this change
removes due process rights of an appellant and should not be at the
discretion of AMS. Other comments requested changes to appeal filing
timeframes and delivery confirmation.
Responses to Public Comment
(Comment) Comments opposed the change to not require AMS to
initiate the hearing process following an appeal denial.
(Response) AMS made changes to Sec. 205.681(a)(2) and (b)(2) to
state that AMS will begin formal administrative proceedings once an
appeal is denied. Those sections also explain that an administrative
proceeding would not begin if the appellant waives or fails to timely
request a hearing or AMS and the appellant reach a settlement
agreement. This revision does not change AMS's intent that appellants
always have the right to request a hearing following a denial of an
appeal; it only provides options for a more expedient resolution in
lieu of a hearing if the appellant consents to that outcome.
(Comment) AMS received comments stating that the proposed revisions
to Sec. 205.681(b) do not clearly provide appeal rights for certifying
agents.
(Response) Person, as defined in the regulations at Sec. 205.2,
includes certifying agents and Sec. 205.681(b) allows persons to
appeal an adverse action by the NOP Program Manager. Further, Sec.
205.681(b)(1) explains what happens to accreditation when an appeal is
sustained.
(Comment) AMS received comments suggesting that dated return
receipts should be replaced with documented delivery confirmation.
(Response) AMS interprets dated return receipts to include
electronic confirmation of electronic delivery, such as registered
email which shows that a message has been delivered to recipient's
email and the date of delivery.
(Comment) AMS received comments that appeals should be filed within
30 days of date of notice rather than date of receipt of notice.
(Response) AMS is not making this change because it could interfere
with due process rights of an appellant. We believe that appellant
should have the full 30 days to appeal from the time that they receive
the notice and not lose time due to possible delays in the mail or
delivery service. Therefore, we are keeping this timeframe to 30 days
from the date of receipt of notice to ensure that appellants have 30
days to review the notice and to decide how to respond.
(Comment) Comments requested that NOP timely respond to appeals
because operations are allowed to remain certified during the appeal
process and any subsequent hearing proceeding.
(Response) AMS has procedures to thoroughly and efficiently
evaluate NOP appeals. AMS generally resolves appeals within 6 months of
receipt. AMS also frequently uses settlement agreements to resolve
appeals which decreases the number of appeals that may potentially
proceed to a hearing.
N. Producer Group Operations
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definitions for Producer group member, Producer group
operation, Producer group production unit, and Internal
control system.
205.201............................................. Organic production and handling system plan.
Paragraph (c).
205.400............................................. General requirements for certification.
Paragraph (g).
205.403............................................. On-site inspections.
Paragraph (a)(2).
----------------------------------------------------------------------------------------------------------------
[[Page 3593]]
The organic industry has a longstanding practice of certifying
groups of producers. This practice helps small farmers access the
organic market and enables handlers to source products that are not
produced in the United States. Compared with traditional producers and
handlers, these groups of producers have unique needs in quality
control and compliance. AMS is establishing requirements for producer
group operations that promote consistent certification practices and
ensure their continued viability and integrity. This rule codifies key
provisions of the 2002 and 2008 NOSB recommendations on producer group
certification, including:
Establishing eligibility criteria for operations to
qualify as producer group operations.
Clarifying the function and responsibilities of Internal
Control Systems (ICS).
Clarifying inspection requirements for producer group
operations.
Additionally, this rule builds upon the NOSB recommendations with
additional detail based on public comment and NOP's programmatic
experience auditing certifying agents and witnessing producer group
inspections. These additions include requirements for more specific ICS
requirements, more specific member and group information in OSPs, and
an improved inspection sampling rate.
This rule strengthens the oversight of organic supply chains by
enabling certifying agents to more readily assess a producer group
operation's compliance with the USDA organic regulations. Certifying
agents and operations that are certified as part of a producer group
may be affected by these requirements. Readers should carefully review
the regulatory text and policy discussion to determine if the
requirements apply to them.
Background
Producer group operations export important organic agricultural
products to the United States, such as coffee, cocoa, bananas, tea, and
spices.\44\ Globally, there are about 2.6 million organic producers
organized across 5,900 producer group operations in 58 countries
(mainly in Africa, Asia, and Latin America), managing a total area of
about 4.5 million hectares (11 million acres) of certified organic
land.\45\
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\44\ Producer groups may also be called ``grower groups.'' The
latter term is commonly used when certification of group operations
is limited to the production or harvest of crops or wild crops.
\45\ Florentine Meinshausen, Toralf Richter, Johan Blockeel and
Beate Huber Project: Consolidation of the Local Organic
Certification Bodies--ConsCert (2014-2018)//March 2019 https://orgprints.org/id/eprint/35159/7/fibl-2019-ics.pdf.
---------------------------------------------------------------------------
Producer group operations present unique certification challenges.
Producer groups may have thousands of members spread across a large
area. The collection, handling, and processing of crops may be
centralized, and these groups may also rely on centralized input
procurement, training, and marketing to sell their product. These
centralized practices can introduce risks to traceability and organic
integrity due to producer group operations' unique structure, size, and
reliance upon internal quality control systems (the ICS) as the first
layer of oversight. Through certification audits and field visits, USDA
has witnessed many of the common problems created by the lack of a
codified producer group standard.
The most common, and difficult to address, challenge is lack of a
well-functioning ICS. The ICS is the first line of oversight and
enforcement and is responsible for critical functions such as education
and inspection of members, and ensuring adherence to the organic
regulations. A poorly functioning ICS often leads to poorly trained
members who do not understand basic organic principles, and the ICS's
lack of effective oversight means members' mistakes go unreported,
resulting in a breakdown of the basic oversight necessary to ensure
that products meet the USDA organic standard. As a result, NOP audits
have uncovered issues such as application of prohibited synthetic
fertilizers and pesticides, mixing of conventional and organic
products, decentralized storage that causes mixing and contamination,
and poor or nonexistent recordkeeping that makes traceability and
verification of integrity difficult. These issues sometimes persist
because the current regulations lack ICS responsibilities and NOP
therefore has no mechanism or basis for citing noncompliance.
Conflict of interest can also become a challenge if not
specifically addressed by the ICS. Often, ICS personnel are relatives
or friends of the members and may withhold or obscure evidence of
noncompliance or fraud. In other cases, the influence of a buyer or
exporter will lead members to compromise organic integrity in order to
meet specific quality or volume targets.
In addition to the ICS, the lack of general criteria that producer
groups must meet creates challenges for certifying agents. This is most
often seen as an absence of critical information about the producer
group and its members. Producer groups often do not provide certifying
agents with basic information, such as accurate maps, location of
plots, acreage, and production practices and inputs. During inspection,
certifying agents commonly cannot locate members, plots, boundaries, or
central distribution points, making it difficult to complete basic
audit techniques such as yield analysis or mass balance.
The unique conditions of producer group production mentioned above,
when combined with poor oversight and enforcement mechanisms at the ICS
level, create an environment where loss of organic integrity and
organic fraud are more likely to occur. The organic regulation
currently does not have the specificity to address these unique
challenges, making it challenging to both discover and correct issues
that are prevalent in producer groups. The provisions in this rule
codify specific eligibility criteria, ICS requirements, and inspection
techniques to address these challenges, and the rule will give
certifying agents the ability to successfully certify and oversee
producer group operations and the products they produce.
The International Federation of Organic Agriculture Movements
(IFOAM) \46\ started developing criteria for producer group
certification in 1994, and in 2003 published its position on ``Small
Holder Group Certification for organic production and processing'' to
support the concept.\47\ The criteria formed the basis for acceptance
of producer group certification in the European Union (EU) and the
United States. Producer group operation certification is also used by
other standards organizations, such as the International Accreditation
Forum and Global G.A.P., to provide small-holder farming operations
access to markets, expand consumer choices, and ensure the integrity of
the supply chain.\48\
---------------------------------------------------------------------------
\46\ https://www.ifoam.bio/.
\47\ https://www.ifoam-eu.org/sites/default/files/page/files/small_holder_group_certification_0.pdf.
\48\ https://www.iaf.nu/; https://www.globalgap.org/uk_en/.
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[[Page 3594]]
Organic certification standards for producer group operations
support strong and consistent oversight and enforcement of producer
group operations. This final rule addresses 2002 and 2008 NOSB
recommendations on producer group certification and adds detail about
documentation requirements and inspection methods in response to public
comments to the proposed rule.\49\ While there are only a few known
producer groups in the U.S. at this time, setting requirements for
producer groups may help U.S. producer group members access the organic
cost-share program and crop insurance. These regulations support the
legitimate status of U.S. producer group members as part of an organic
operation.
---------------------------------------------------------------------------
\49\ NOSB Recommendation: Criteria for Certification of Grower
Groups. October 20, 2002: https://www.ams.usda.gov/sites/default/files/media/Rec%20Criteria%20for%20Certification%20of%20Grower%20Groups.pdf.
NOSB Recomendation: Certifiying Operations with Multiple
Production Units, Sites, and Facilities under the National Organic
Program. November 19, 2008: https://www.ams.usda.gov/sites/default/files/media/NOP%20Final%20Rec%20Certifying%20Operations%20with%20Multiple%20Sites.pdf.
---------------------------------------------------------------------------
Qualifying as a Producer Group Operation
Certifying agents must assess whether operations that apply for or
maintain producer group certification meet the characteristics in the
definitions for producer group member, producer group operation, and
producer group production unit and the qualifications for certification
as producer group operations in 205.400(g). Operations that do not meet
all criteria must not be certified as a producer group operation.
The smallest unit of a producer group operation is a producer group
member. A producer group member is an individual engaged in the
activity of producing or harvesting agricultural products as a member
of a producer group operation. The practices of each producer group
member must align with the organic system plan (OSP) of the producer
group. Each member must use practices that comply with the requirements
for producers and handlers in the USDA organic regulations. Some
requirements may be met collectively by the producer group operation,
such as submitting an organic system plan.
Producer group members are organized into production units. A
producer group production unit is a defined subgroup of producer group
members in geographic proximity within a single producer group
operation that use shared practices and resources to produce similar
agricultural products. Each producer group operation determines the
producer group production units in its operation and must identify
these in the organic system plan per Sec. 205.201(c)(4).
A producer group operation is a producer, organized as a person,
consisting of producer group members and production units in geographic
proximity governed by an internal control system under one organic
system plan and certification. A producer group operation must define
its geographic proximity criteria for its producer members and
production units Sec. 205.201(c)(4). The site-specific conditions of
an operation, such as infrastructure, topography, common soil, water
source, and products produced will affect ``geographic proximity.''
Therefore, AMS is requiring that certifying agents document and adopt
their own criteria or guidelines for internal consistency when
establishing acceptable distances or evaluating the geographic reach of
a producer group operation.
Producer group operations may be certified for crops, wild crops,
livestock, and handling. The requirements for production and handling
operations in the USDA organic regulations also apply to producer group
operations.
Structure and Organization of Producer Group Operations
A producer group operation must be organized as a person (Sec.
205.400(g)(1)). Organization as a person provides a path to
certification because OFPA and the USDA organic regulations apply to a
person as the basic regulatory unit. The definition for person at 7
U.S.C. 6502(16) and Sec. 205.2 includes groups (e.g., ``. . .
association, cooperative, or other entity''). Therefore, certification
may be granted to the producer group operation, rather than individual
producer group members.
A producer group operation must use centralized processing,
distribution, and marketing facilities and systems (Sec.
205.400(g)(2)). A group may have several facilities for aggregating the
products of producer group members and production units and moving into
commerce.
An internal control system (ICS) is a defining component of
producer group operations and is critical for management of the
operation. The ICS is an additional tier of oversight and enforcement
between the producer group members and the certifying agent. All
producer group operations must have an ICS that implements the
practices and procedures described in the organic system plan (Sec.
205.400(g)(4)). Further ICS requirements are discussed in the following
section.
All products sold, labeled, or represented as organic by a producer
group operation must be produced or harvested only by producer group
members on land and using facilities that are included in the producer
group operation's certification (Sec. 205.400(g)(5)). This means that,
for example, a producer group member from one operation (A) must not
use a handling facility owned by another producer group operation (B)
unless the facility is included in the organic system plan and the
producer group operation's (A) certification. A producer group
operation must not buy products from non-member producers and sell,
label, or represent them as organic using the producer group
certification. Likewise, producer group members must not sell, label,
or represent their products as organic outside of the producer group
operation unless they are individually certified (Sec. 205.400(g)(6)).
This accommodates producer group operations with members of varying
production levels where some members have the capacity and need for
marketing channels in addition to the producer group operation. When
this occurs, clear and careful recordkeeping is essential for
successful mass-balance audits.
Producer group operations must provide a comprehensive inventory of
the producer group operation and its capacity to the certifying agent.
Specifically, the operation must provide the name and location of each
producer group member and producer group production unit(s), and
identify all products produced, estimated yield(s), and the sizes of
the production and harvesting areas (Sec. 205.400(g)(7)). Producer
group operations must provide this information to the certifying agent
at least annually and should inform the certifying agent more
frequently of changes that may affect its compliance with OFPA or the
USDA organic regulations, e.g., additional crops produced, inclusion of
new land area and producer group members.
Producer group operations must also show evidence of compliance
with the USDA organic regulations through internal inspections and
reporting sanctions imposed on producer group members. It is not
feasible for certifying agents to inspect each producer member
annually, due to the number of members in any one producer group
operation. However, the producer member must attend the internal
inspection to provide complete information about their
[[Page 3595]]
production activities (Sec. 205.400(g)(8)). Internal inspections must
include mass-balance audits and reconciliation of each producer group
member's and each producer group production unit's yield and group
sales. Records are critical to demonstrate compliance and producer
group operations must maintain a recordkeeping system so that products
are traceable from producer group members' individual production parcel
to aggregation and handling at the production unit and through sale or
transport when the products leave the custody and ownership of the
producer group operation (Sec. 205.400(g)(9)).
Internal Control Systems
Pursuant to the 2002 NOSB recommendation ``Criteria for
Certification of Grower Groups'' \50\ and an August 2020 IFOAM position
paper,\51\ all producer group operations must have an internal control
system (ICS). The internal control system is an internal quality
management system that establishes and governs the review, monitoring,
training, and inspection of the producer group operation, and the
procurement and distribution of shared production and handling inputs
and resources, to maintain compliance with the USDA organic
regulations. The ICS consists of both the personnel and the procedures
that form a producer group's internal governance, verification, and
enforcement system. The ICS is responsible for the overall governance
and compliance of the producer group operation and verifies each
member's adherence to the organic system plan and USDA organic
regulations.
---------------------------------------------------------------------------
\50\ NOSB Formal Recommendation, Criteria for Certification of
Grower Groups, October 20, 2002: https://www.ams.usda.gov/sites/default/files/media/Rec%20Criteria%20for%20Certification%20of%20Grower%20Groups.pdf.
\51\ ``Internal Control Systems (ICS) for Group Certification,''
IFOAM Organics International, August 2020, https://www.ifoam.bio/our-work/how/standards-certification/internal-control.
---------------------------------------------------------------------------
ICS Functions
A producer group operation must have an OSP that meets the
requirements for all operations in Sec. 205.201(a) and additionally
must describe its ICS procedures and practices. Section 205.201(c)
describes the OSP requirements that are specific to producer group
operations. The OSP for a producer group operation needs to include a
description of the ICS and how it verifies the operation's compliance
with the USDA organic regulations. This includes defining the
organizational structure, roles, qualifications, and responsibilities
of all ICS personnel (Sec. 205.201(c)(1)). Personnel qualifications
could include, for example, knowledge of local production practices,
organic production and handling practices, ICS procedures, USDA organic
regulations, and fluency in the language(s) of the producer group
operation.
The ICS must also describe and prevent conflicts of interest
between ICS personnel and the producer group operation that it oversees
(Sec. 205.201(c)(3)). The USDA organic regulations identify conflict
of interest scenarios for certifying agent and operations (Sec.
205.501(a)(11)). The ICS personnel-producer member relationship is
different than the certifying agent-certified operation relationship so
these criteria are not wholly applicable to producer group operations.
For example, certifying agents are not permitted to consult with
operations to overcome obstacles to certification. However, ICS
personnel are required to provide training, education, and resources to
assist producer members with awareness of, and compliance with, organic
requirements. A generally accepted criteria for conflict of interest is
whether an oversight entity, e.g., the ICS, has a financial interest in
the regulated party or likely bias based on familial relations. For
example, internal inspectors should not inspect family members or
production units where the inspector is a member.
The oversight function of the ICS places its personnel at a higher
risk for retribution from producer group operations. To support the
integrity of ICS oversight, the ICS must also describe how it will
protect ICS personnel from retaliation for carrying out their
responsibilities, and, in particular, finding and reporting
noncompliances (Sec. 205.201(c)(3)). This could include obtaining a
written guarantee from the producer group operation that ICS personnel
will not be subject to retribution and requiring ICS personnel to
disclose any conflicts of interest prior to internal inspections or
review.
The ICS must document and apply procedures for adding new members
to a producer group operation (Sec. 205.201(c)(5)). These procedures
must cover how each new member will be inspected by the ICS and
evaluated to determine whether they can fully comply with the organic
production and handling requirements before they are added as a
producer member.
Producer group members use common practices to produce, harvest,
and handle their collective products and common inputs. Shared farming
or harvesting practices could include fertility and pest management,
procurement of inputs (including seeds or soil amendments), and shared
resources could include post-harvest handling facilities. The ICS must
describe how shared resources, including production practices and
inputs, are procured and provided to all producer group members and
personnel (Sec. 205.201(c)(7)). Shared practices and inputs are
critical to fostering compliance among many individual farmers and
documenting these practices is an important indicator of compliance for
the entire operation. Training, education, and technical assistance are
critical practices to support consistent and compliant practices among
producer members and the description of the ICS must explain how these
resources are provided (Sec. 205.201(c)(8)).
Internal Oversight
The ICS is the first line of oversight of a producer group
operation and is responsible for assessing the compliance of producer
group members. The USDA organic regulations include several
requirements to ensure that the ICS provides competent and thorough
oversight. More generally, the ICS must have documented clear policies
and procedures to verify the producer group operation's and producer
group members' compliance with the USDA organic regulations (Sec.
205.201(c)).
The ICS must identify criteria for high-risk producer group members
and production units (Sec. 205.201(c)(6)). Certifying agents must also
determine which producer members are high risk. Examples of risk
factors that may be used by both the ICS and the certifying agent are
listed below in the discussion of on-site inspection by the certifying
agent.
Clear and comprehensive records are a critical component of an ICS.
They help certifying agents understand how the operation is
implementing its organic system plan and complying with the USDA
organic regulations. The organic system plan must describe the system
of records maintained by the ICS (Sec. 205.201(c)(9)). The system of
records must show how records will support and be used for mass-balance
calculations and traceability throughout the operation. For full
traceability, records would need to cover the purchase, acquisition, or
production of products for each producer member through sale or
transport.
The description of the ICS must explain internal monitoring,
surveillance, sanctions, inspection, and auditing methods used to
assess compliance of all producer group
[[Page 3596]]
members (Sec. 205.201(c)(10)). As a best practice, internal monitoring
and surveillance should cover critical organic control points may
include, for example, buffer areas, condition of crops and/or wild
crops and animals, soil quality indicators, handling practices, input
and equipment use and storage areas. A description of sanctions may
cover the review of internal inspection results to determine member
compliance; and the processes to address noncompliances, impose
sanctions, remove noncompliant producer group members and reporting
noncompliances to the certifying agent. A description of the auditing
methods could cover mass-balance audits to reconcile the expected and
actual yields and sales of producer members, producer group production
units, and producer group operations.
On-Site Inspections by the Certifying Agent
Certifying agents are the second tier of oversight for producer
group operations. Certifying agents, in addition to verifying that
producer group operations are fully compliant with the eligibility,
certification and ICS requirements, must follow specific requirements
for on-site inspections of producer group operations. Initial and
annual on-site inspections of producer group operations must comply
with the general requirements for inspections in Sec. 205.403. During
annual on-site inspections of producer group operations, certifying
agents are required to evaluate the ICS, review internal inspections
conducted by the ICS of individual members, and observe ICS personnel
conducting internal inspections (Sec. 205.403(a)(2)(i)-(ii)). At least
one producer group member from each producer group production unit must
be inspected, and each handling facility, including all collection
sites, must be inspected (Sec. 205.403(a)(2)(iii)-(iv)). Collection
sites, where the harvest from multiple producer group members is stored
before transport, are handling facilities, and are inspected by
certifying agents. USDA organic regulations do not set a minimum number
or percentage of witness inspections that a certifying agent must
conduct at each producer group operation inspection. Witness
inspections are a key component of assessing the ICS and certifying
agents will need to ensure that the number of witness inspections at a
given operation is sufficient to evaluate ICS rigor.
During on-site inspections, certifying agents must inspect at least
1.4 times the square root or 2% of the total number of producer group
members, whichever is higher (Sec. 205.403(a)(2)(iii)).\52\ The square
root sampling rate aligns with industry practice. Two sampling rates
are provided because the power of the square root sampling power begins
to decline when operations exceed 5,000 members so that a smaller
proportion of members are inspected relative to the total number of
members. The addition of the 2% rate more evenly distributes the number
of external inspections across producer groups regardless of the number
of members as shown in Table 1. For each producer group operation,
certifying agents need to calculate the number of members to inspect
using the square root method and the 2% rate and use the higher number.
---------------------------------------------------------------------------
\52\ The square root sampling scheme was developed in the 1920s
as a sampling scheme for agricultural regulatory inspectors. The
formula used was the square root (Sqrt) of the lot size (N) + 1.
Blanck, F.C. (1927). ``Report of the Committee on Sampling,'' J.
Assoc. Official Agricultural Chemists, 10, 92-98.
Table 1--Certifying Agent ICS Inspection Sampling Rates
----------------------------------------------------------------------------------------------------------------
Producer group members (N) Square root Flat 2% Final rule
--------------------------------------------------------------- method ---------------------------------
---------------- Greater of 1.4 *
N 1.4 * [radic]N 2% [radic]N or 2%
----------------------------------------------------------------------------------------------------------------
50............................................................ 10 1 10
100........................................................... 14 2 14
250........................................................... 23 5 23
500........................................................... 32 10 32
1000.......................................................... 45 20 45
5000.......................................................... 99 100 100
7500.......................................................... 122 150 150
10000......................................................... 140 200 200
----------------------------------------------------------------------------------------------------------------
The number of producer group members inspected by the certifying
agent must include all high-risk members (Sec. 205.403(a)(2)(iii)).
Certifying agents must inspect at least one producer group member in
each production unit (as defined in Sec. 205.2) to ensure all producer
group production units are inspected, as well as each handling
facility. As a best practice, AMS recommends that certifying agents
also select members from across the risk spectrum--including lower-risk
members--so that the same producer members are not inspected year after
year. This may require a sample size larger than the minimum required
(i.e., more than 1.4 times the square root or more than 2% of the
number of producer group members). All numbers must be rounded up to
the next whole number (e.g., using square root method, 50 members = 10
inspections, 100 members = 14 inspections, 500 members = 31
inspections, and 1,000 members = 44 inspections). The certifying agent
has the discretion to inspect more producer group members than the
minimum indicated by the calculation.
Risk-based inspections rely upon certifying agents having policies
and procedures to determine the risk factors associated with producer
group operations. While the ICS determines which producer members and
production units are high-risk according to their criteria, the
certifying agent needs to independently determine which members are
high-risk (Sec. 205.403(a)(2)(iii)). The certifying agent should apply
the risk assessment procedures to determine and instruct the inspector
on which producer group members to inspect during the annual
inspection. After all risk-based and other inspection selection
criteria are satisfied, certifying agents should randomly select the
remaining member inspections so that different lower-risk producer
group members are inspected each year.
Risk factors may include, but are not limited to, producer group
administrative capacity, organization complexity, and variations in
members and production units (such as product quantity and value,
member size,
[[Page 3597]]
number of products), rate of growth, and compliance and enforcement
history. For example, a producer group member selling products outside
of the producer group or a producer group member that is considerably
larger than the other producer group members in a production unit
represent compliance risks to the overall producer group operation.
When assessing the risks of the producer group operation to determine
which producer group members to inspect, examples of risk factors that
the certifying agent may consider include, but are not limited to:
Noncompliance history of overall producer group and of
individual members;
The criteria used to designate a collection of producer
group members as a single producer group production unit;
High-risk members identified in the ICS and producer
groups member with noncompliances;
Application of prohibited materials adjacent to member
fields;
Split or parallel operations (i.e., operations that are
also producing nonorganic agricultural products);
Producer group members with incomes greater than $5,000
USD per year;
The procurement, availability, and distribution of inputs
and resources to members;
The prevalence of nonorganic production of similar
products and crops in the region;
Post-harvest handling practices designed to prevent
commingling and contact with prohibited substances;
New producer group members;
Size of producer group member's production or gathering
areas; and
Significant expansion of a producer group member's
production area.
As a best practice, the inspection of the ICS should also include:
document review; auditing of production and sales/distribution records;
reconciliation of product inventory; review of procurement and
distribution of inputs; review of the inspections conducted by the ICS;
review of ICS personnel qualifications and training; witness audits to
observe ICS inspectors; review of noncompliance actions for producer
group members; examination of organic control points and high-risk
areas; interviews with managers responsible for the OSP, governance of
the ICS, and producer group members and individuals overseen by the
ICS; and review of training provided to ICS staff and producer group
members.
Summary of Changes to Final Rule
AMS made several changes to the proposed regulatory text when
writing this final rule. Changes to the final rule are discussed below
and are followed by responses to specific themes from public comment.
AMS revised the definitions of producer group member,
producer group operation, producer group production unit and internal
control system to allow livestock production and to clarify that the
operation is regulated as a person. Use of the term ``individual'' in
producer group member and ``person'' in producer group operation more
clearly indicates that the operation is the legal regulated entity,
which is consistent with current regulation and ties to the existing
defined term person (see Sec. 205.2).
AMS replaced ``crop/wild-crop'' with ``agricultural
product'' throughout so that livestock and livestock products are not
excluded from producer group operation production. Public commenters
argued that a prohibition on livestock in producer group certification
may disproportionately affect poor and small-scale farmers that depend
on producer groups to access the organic market. Livestock production
in producer group certification is consistent with EU organic
standards, IFOAM, the 2008 NOSB recommendation, and current practice in
the organic industry. Allowing livestock production avoids market
disruption and negative impact to operations that depend on producer
group certification for market access.
AMS added more specificity to the description of the ICS
in the organic system plan, including: describing qualifications of ICS
personnel; procedures for approving new members; policies to protect
ICS personnel from retribution; description of technical assistance to
members; and a system of records that covers each member and support
mass-balance audits and traceability. Public comments stressed the
importance of the ICS and suggested modifications to strengthen the
ICS's ability to enforce the organic regulations and maintain organic
integrity. AMS agrees with public comments and has revised ICS
requirements to be more specific because this is necessary to bolster
the oversight and enforcement of producer groups.
AMS clarified that producer group operations must only
sell products from the land and facilities included in the
certification. The proposed text only specified ``from grower group
members.'' Additionally, requiring that producer groups only sell
products produced using land and facilities within the certified
operation improves oversight because these facilities and land are
routinely inspected by the ICS and the certifying agent.
AMS added a requirement that producer group operations
must maintain an ICS as described in the organic system plan. Although
it was implied, proposed Sec. 205.400(g) did not include an explicit
requirement to maintain an ICS and did not reference the ICS
requirements (Sec. 205.201(c)). Adding this explicit requirement makes
an ICS a clear condition of certification that must be included as part
of an organic system plan.
AMS clarified that producer group members must be present
during internal inspections. Having producer group members present
during onsite internal inspections is necessary so that ICS personnel
can interact with and ask questions of the members to ensure a full
understanding of the activities on the members' production sites.
AMS removed a redundant requirement from Sec. 205.400(g)
that the producer group operation must document and report the use of
sanctions; the description and implementation of a system of sanctions
is covered in Sec. Sec. 205.201(c)(10) and 205.400(g)(4) and (10).
AMS adjusted the sampling rates certifying agents must use
when inspecting producer groups to 1.4 times the square root or 2% of
the total number of producer group members, whichever is higher. The
proposed inspection rate of 1.4 times the number of members is a
digressive rate, which samples a smaller percentage of members as a
group grows larger. Combining this with a linear 2% sampling rate
ensures that larger producer groups (those with more than 5,000
members) are inspected at a similar rate as smaller groups.
AMS revised Sec. 205.403(a)(2)(iii) to clarify that a
certifying agent must inspect all producer group members determined to
be high-risk by the certifying agent. The proposed rule had stated that
high-risk members should be chosen based on the ICS's risk criteria.
This change improves oversight by ensuring that a certifying agent
conducts independent risk assessments based on their own risk criteria,
rather than relying only on the ICS's assessment.
Summary of Public Comments
The majority of public comments received supported AMS's
codification of producer group standards in the USDA organic
regulations. Many comments provided suggestions and
[[Page 3598]]
recommendations to the proposed policy.
Many comments strongly opposed the proposed prohibition of
livestock production within producer groups, requesting that AMS revise
the standard to allow ``scope neutrality'' and the production of
livestock and livestock products. Several commenters stated that many
certified producer groups already produce livestock and livestock
products, and that prohibiting livestock would negatively impact these
operations.
Several comments suggested AMS add more specificity to the proposed
ICS requirements to ensure the ICS can manage the unique challenges of
producer groups. Commenters requested more detail about conflict of
interest, training, risk assessment, inspections, recordkeeping,
personnel qualifications, protections for farmers, and evaluation of
the ICS by the certifying agent. Commenters pointed to specific details
found in the preamble describing organic system plans and the internal
control system and requested these be added to the final rule to
support clarity and consistency.
The proposed rule asked if producer group risk should be managed by
placing limits on scale (e.g., number of members, size of individual
members, geographic distribution of members). Most commenters agreed
that the risks of uncontrolled size or scale should be addressed but
felt prescriptive limits may arbitrarily exclude members, disrupt well-
functioning groups, restrict economic opportunity, or force producers
to revert to conventional methods. The majority of commenters advocated
for ``scale neutrality'' and requested NOP develop alternate strategies
to manage the risks of large producer group operations.
Several comments requested that AMS require the use of risk
criteria and assessment to control issues of scale. Others recommended
that AMS develop a separate scope of accreditation specifically for
producer groups, arguing that certification of these operations
requires specialized skill and oversight. A few comments noted the
difficultly of identifying producer groups in the Organic Integrity
Database, and asked for identification to be mandatory. Some comments
noted differences between the proposed policy and other international
standards, and asked AMS to align its producer group standards with EU
and IFOAM. Finally, a few comments expressed concern that the producer
group standard may be used by large livestock or poultry cooperatives
in the United States, which they argue is against the intent of the
standard to support opportunity and growth for very small organic
farmers.
Responses to Public Comments
(Comment) Some commenters recommended specific limits on parcel
size and number of members in a producer group operation because a lack
of controls on scale could lead to inadequate and inconsistent
enforcement. Commenters mentioned that an ICS could be reluctant to
enforce against a large producer member without which the producer
group could fail.
(Response) AMS is not setting size limitations, in terms of land
area or number of members, on producer group operations. The ICS
requirements support effective oversight of producer group operations
regardless of their size.
(Comment) Comments opposed the proposed prohibition of livestock
producer group operations. Commenters argued that this may
disproportionately affect poor and small-scale farmers that depend on
producer groups to access the organic market. Some comments mentioned
that livestock producer group operations are already certified for beef
and honey production.
(Response) AMS revised the proposed rule to allow the certification
of livestock production as producer group operations. This allowance
aligns with the EU organic standards for producer group operations and
the 2008 NOSB recommendation, which did not restrict producer group
certification to crop and wild crop operations. Livestock producer
group operations may be more complex and higher risk than crop and wild
crop producer group operations. In practice, this will require careful
oversight of the ICS and qualifications of ICS inspectors and
personnel. Further, some types of livestock production may be
unsuitable for group certification (e.g., intensive livestock farming,
variability between producer members) because it is more difficult for
them to meet the requirements for certification as a producer group
operation.
(Comment) Comments requested a separate scope of accreditation for
producer group certification to ensure that certifying agents are
sufficiently qualified to certify producer groups.
(Response) Establishing a separate scope of accreditation would
require more input and assessment of impacts, as this was not included
in the proposed rule. This type of certification is complex and
presents higher risks for organic integrity. AMS will assess certifying
agents' oversight of and qualifications for producer group
certification through rigorous audits.
(Comment) Comments suggested that the ICS should describe the
qualifications of all ICS personnel and the procedure to ensure the
availability of a sufficient number of qualified personnel. Comments
specified that the ICS should describe how ICS personnel are familiar
with the local production practices, general organic production and
handling practices, the USDA organic regulations, ICS procedures and
regulations, and be fluent in the language(s) of the producer group
members and the ICS.
(Response) The description of the ICS must describe the
qualifications and responsibilities of ICS personnel. AMS has
identified examples of the knowledge qualifications for ICS personnel,
but is not adding these as required to give flexibility to certifying
agents to determine the suitable qualifications on specific operations.
(Comment) Comments asserted that producer group operations must
ensure that all group members understand and can comply with the USDA
organic regulations. Commenters urged that the ICS should describe how
the training, education, and technical assistance that is provided to
producer group members and ICS personnel ensures their understanding of
and compliance with internal control system's policies, the organic
system plan, and the USDA organic regulations.
(Response) Producer group operation compliance requires that each
member understand the required and prohibited practices for organic
production and handling. AMS has added a requirement for the ICS to
include training, education, and technical assistance to producer
members (205.201(c)(8)). Given that producer group operations are
located in areas with varying language and literacy proficiency, it is
the responsibility of the operation to effectively communicate this
information to all members on an ongoing basis.
(Comment) Comments stated that the ICS should explain how it
manages conflicts of interest by addressing or prohibiting internal
inspectors from inspecting or acting as buying officers for their own
relatives. Comments also requested guidance around conflict-of-interest
scenarios and that internal inspectors are not restricted from
providing training, education, or technical assistance to producer
group members.
(Response) The description of the ICS must explain how it will
prevent potential conflicts of interest. The development of guidance on
specific examples of conflict of interest needs further public input
and discussion and
[[Page 3599]]
that level of detail was not included in the scope of this rule.
Certifying agents will review the ICS to determine if known potential
conflicts of interest are identified and prevented. AMS agrees that
internal inspectors inspecting or procuring products from their
relatives would be potential conflicts of interest because the
relationship may compromise the inspector's objectivity in assessing
compliance.
(Comment) Comments stressed that group members need to be present
during their internal inspection and that more guidance is needed to
ensure the ICS is addressing noncompliances and reporting major
noncompliances to the certifying agent.
(Response) AMS has added the requirement for producer members to be
present at the inspection of their production site(s). Maintaining an
organized, transparent, and equitable system of sanctions is critical
for producer group certification. The ICS must have procedures for
implementing a system of sanctions, and the producer group operation
must report sanctions for noncompliant members to the certifying agent.
The requirements for recordkeeping that covers internal inspection
reports, sanctions, and corrective actions plus the external inspection
requirements will help certifying agents to assess whether the ICS is
reporting noncompliances and sanctions to the certifying agent.
(Comment) Comments supported that the ICS describe the
recordkeeping system that must cover signed member agreements, internal
inspection reports, documents related to internal sanctions and
corrections, and formal agreements for each producer group member that
commits them to complying with ICS, OSP, and USDA organic regulations,
along with all training records for members and personnel. The ICS
procedures should state how lists of individual members, locations,
products, acreage, copies of inspection reports, sanctions, and
corrections are stored and made available during inspection by the
certifying agent.
(Response) The USDA organic regulations require a description and
implementation of the recordkeeping system. The critical objective of
recordkeeping is to support traceability of production, inputs, and
transactions throughout the producer group operation. Information about
sanctions and internal inspection reports are required by separate
provisions.
(Comment) Comments requested clarification about what types of
noncompliances (i.e., major vs minor) must be reported to the
certifying agent.
(Response) The requirement to report noncompliances to the
certifying agent enables the certifying agent to assess ICS oversight.
It also leaves flexibility for the ICS to describe different timing and
reporting methods for noncompliances of varying scope and severity.
Noncompliances that may result in removal of the member(s) from the
producer group, for example, application of prohibited substances,
warrant timely notification to the certifying agent. In contrast,
maintaining records of correctable noncompliances for the certifying
agent to review during external inspections would be acceptable.
(Comment) Comments stated that the use of 1.4 times the square root
of the number of members is not adequate for external inspections. They
explained that this inspection rate is either too low for a producer
group with more than 5,000 members, resulting in potentially inadequate
oversight of very large groups, or the inspection rate is too high and
burdensome for small producers, resulting in pressure to grow larger to
reduce certification costs. Comments suggested other rates including a
flat percentage rate of 2-3%, a combination of square root and flat
rate methods, or a minimum of 10% of producer group members.
(Response) The external inspection sampling rate should be equally
stringent for producer member operations regardless of size. The USDA
organic regulations specify that certifying agents must use the higher
result of 2 sampling rates to set the minimum number of producer
members that need to be inspected. Setting 2 rates is necessary because
the square root sampling power begins to decline when producer groups
are larger than 5,000 members. The use of 1.4 times the square root or
2% of the total number of producer members is a minimum and does not
prevent certifying agents from using sampling sizes that exceed the
results of those rates. Higher levels of inspection rates may be
warranted when necessary if a producer group operation has a history of
inadequate internal controls and poorly trained personnel with
ineffective policies, procedures, or sanctions, and is failing to
enforce against noncompliant members, failing to inspect all members,
or is not completing mass-balance audits.
O. Calculating the Percentage of Organically Produced Ingredients
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.302............................................. Calculating the percentage of organically produced
ingredients.
Paragraphs (a)(1), (2), and (3).
----------------------------------------------------------------------------------------------------------------
This rulemaking revises Sec. 205.302(a) to clarify that the
percentage of organic ingredients in multi-ingredient products should
be calculated by dividing the weight or volume of the organic
ingredients at formulation by the total weight or volume of the product
at formulation, with water and salt added as ingredients at formulation
excluded from the calculation.
This policy may affect certified operations, noncertified
operations that process products containing organic ingredients,
applicants for organic certification, and certifying agents. The reader
should carefully examine the regulatory text and discussion below.
Background
Section 205.301 of the organic regulations classify products
containing organic ingredients into several categories based on percent
composition--e.g., ``100 percent organic,'' ``organic,'' ``made with
organic (specified ingredients or food group(s)).'' Clear and easily
understood instructions for calculating product composition are needed
to ensure consistent classification by the organic industry.
Previous policy had sometimes caused inconsistent implementation
because it required calculation based on ``total weight of the finished
product.'' It was unclear if this meant products before or after
processing. Because processing (e.g., cooking, baking, dehydrating,
freeze drying) often causes water loss from ingredients, using the
total weight of the product after processing sometimes resulted in
inflated percent organic content calculations. This rulemaking
clarifies that organic content must be calculated from the weight of
ingredients at formulation (i.e., before processing such
[[Page 3600]]
as baking or cooking). This will ensure correct calculation of organic
content so that labels on multi-ingredient organic products are
accurately listed. This requirement also addresses an existing point of
confusion and will increase the consistency of organic labeling claims
in processed organic products. This policy is consistent with both an
April 2013 NOSB recommendation \53\ and NOP 5037 Draft Guidance
published by AMS in December 2016.\54\
---------------------------------------------------------------------------
\53\ NOSB Recommendation, Calculating Percentage Organic in
Multi-Ingredient Products, April 11, 2013: https://www.ams.usda.gov/sites/default/files/media/NOP%20CACC%20Final%20Rec%20Calculating%20Percentage.pdf.
\54\ The draft guidance and comments can be viewed at https://www.regulations.gov/document?D=AMS-NOP-16-0085-0001 and in the NOP
Program Handbook: https://www.ams.usda.gov/sites/default/files/media/NOP5037DraftGuidancePercentCalculations.pdf.
---------------------------------------------------------------------------
Calculating Percentage of Organic Ingredients
To calculate the percentage of organic ingredients in a multi-
ingredient product, divide the weight or volume of the organic
ingredients at formulation by the total weight or volume of the product
at formulation. If water and salt are added as ingredients, these must
be excluded from the calculation. If a multi-ingredient product
contains only liquids, volume must be used for calculation. If a
product contains both solid and liquid ingredients, weight must be used
for calculation. Please see Table 2, below, for an example of how to
calculate the percentage organic content of a multi-ingredient product.
Liquid ingredients being reconstituted from concentrates should be
calculated based on single-strength concentrations. The term ``single-
strength'' is defined by the Food and Drug Administration (21 CFR 101)
as equivalent to the Brix value of 100 percent juice. Brix is a
measurement referring to the percent, by mass, of soluble solids
(generally sugar) in a solution. Brix is a useful reference in
identifying single-strength identities of juices (see 21 CFR
101.30(h)(1)) as the mass of sugar and other soluble solids is not
affected by the concentration process (i.e., the same mass of sugar
will be present in 1 liter of apple juice measured at 11.5 Brix, as is
present in 0.5 liters of concentrated apple juice measured at 23 Brix).
Reconstitution is taking a concentrated juice product and adding water
to dilute the concentrated juice back to single-strength values. Using
the previous example, if a producer starts with 0.5 liters of
concentrated apple juice, they could add water to increase the total
volume to 1 liter, bringing the juice back to the original Brix value
of 11.5. Allowing for reconstituting concentrated juice gives producers
flexibility in shipping, storage, and use of juice products in organic
production.
For products that have ingredients composed of multiple ingredients
(also referred to as ``multi-ingredient ingredients''), the exact
organic content should be obtained of that multi-ingredient ingredient
when calculating the total organic content of the final organic
product. In this case, the calculation should identify the organic and
nonorganic parts of the multi-ingredient ingredient and supporting
documentation should be available for the certifying agent to review.
Alternatively, these ingredients should be calculated as contributing
either 95% organic content or 70% organic content depending on how the
product is classified (i.e., either ``organic'' or ``made with organic
(specified ingredients or food groups)'' respectively).
Table 2--Calculating Percent Organic of a Soy Beverage
----------------------------------------------------------------------------------------------------------------
Weight of
ingredient at % Organic % In Actual
Ingredient formulation content of formulation organic %
(lbs.) ingredient
----------------------------------------------------------------------------------------------------------------
Organic Soy Base..................................... 1,100 100 16.42 16.4200
Organic Cane Sugar................................... 5,288 100 78.94 78.9400
Organic Vanilla Extract.............................. 60 95 0.89 0.8455
Vitamins............................................. 50 0 0.74 0.0000
Calcium Phosphate.................................... 100 0 1.49 0.0000
Carrageenan.......................................... 100 0 1.49 0.0000
Added Water.......................................... 10,000
Added Salt........................................... 5
----------------------------------------------------------
Total weight (excluding added salt and water).... 6,698
----------------------------------------------------------
Total % Organic.................................. ............... ........... .............. 96.2055
----------------------------------------------------------------------------------------------------------------
Summary of Changes to the Final Rule
AMS replaced the parenthetical statements ``(excluding water and
salt)'' with the single statement ``Water and salt added as ingredients
at formulation are excluded from the calculation.'' This more clearly
states NOP's intent and will result in more consistent calculation of
organic content across the industry.
Summary of Public Comment
In general, almost all public comments supported AMS's
clarification that percent organic content must be calculated based on
weights/volumes at formulation. However, many comments noted that the
proposed text could be interpreted to mean that salt and water must be
excluded from each ingredient during calculation. Commenters explained
this would be difficult and unnecessary to calculate the amount of
water and salt in some ingredients and asked that AMS revise Sec.
205.302(a) to state that only water and salt added as ingredients
should be excluded from calculation. However, several comments also
asked AMS to clarify that water and salt added to individual
ingredients (e.g., broth or tea) should be excluded from calculation.
Responses to Public Comment
(Comment) Many comments noted that the proposed text could be
interpreted to mean that salt and water must be excluded from
individual ingredients during calculation. Commenters explained this
would be difficult and unnecessary to calculate the amount of water and
salt in some ingredients, and asked that AMS revise Sec. 205.302(a) to
state that only water and salt added as ingredients should be excluded
from calculation.
[[Page 3601]]
(Response) AMS has replaced the parenthetical statements
``(excluding water and salt)'' with the single statement ``Water and
salt added as ingredients at formulation are excluded from the
calculation.'' This clearly states that only water and salt added as
ingredients are excluded from calculation.
(Comment) Several comments asked NOP to clarify how to calculate
percentage organic content when ingredients are composed of more than
one ingredient (a ``multi-ingredient ingredient'').
(Response) The exact organic content of a multi-ingredient
ingredient should be used when calculating the total organic content of
the final organic product.
P. Supply Chain Traceability and Organic Fraud Prevention
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.2............................................... Terms defined.
Definitions for Organic fraud and Supply chain
traceability.
205.103............................................. Recordkeeping by certified operations.
Paragraphs (b)(2), and (3).
205.201............................................. Organic production and handling system plan.
Paragraph (a)(3).
205.501............................................. General requirements for accreditation.
Paragraphs (a)(10), (13), and (21).
205.504............................................. Evidence of expertise and ability.
Paragraphs (b)(4) and (7).
----------------------------------------------------------------------------------------------------------------
Traceability and fraud prevention are essential in complex organic
supply chains. Because protecting and verifying organic integrity is a
responsibility shared by many participants in the organic industry,
this rulemaking requires certified operations and certifying agents to
incorporate supply chain traceability and organic fraud prevention into
their practices. These actions will strengthen organic integrity and
reinforce trust in the USDA organic label.
Certified organic operations must:
Maintain records of their activities that span the time of
purchase or acquisition, through production, to sale or transport;
Maintain records that trace back to the last certified
operations in their supply chain;
Maintain audit trail documentation to facilitate supply
chain traceability, including identification of agricultural products
as organic on audit trail documents; and
Describe in their organic system plan the monitoring
practices and procedures used to prevent organic fraud and verify
suppliers and organic product status.
Certifying agents must:
Conduct risk-based supply chain traceability audits of
products they certify to verify compliance;
Maintain procedures for identifying high-risk operations
and agricultural products, conducting risk-based supply chain audits,
and reporting credible evidence of organic fraud to the USDA; and
Share information with other certifying agents to conduct
investigations, conduct supply chain traceability audits, and verify
compliance of organic products.
These requirements may affect certified organic operations,
certifying agents, and operations applying for organic certification.
Organic stakeholders should carefully examine the regulatory text and
policy discussion below.
Background
Because organic products are credence goods, the organic system
relies upon on trust between entities in organic supply chains.\55\
Therefore, traceability and verification of organic products are
essential to the function of a healthy organic market. This is
especially true of modern organic supply chains, which have grown
longer and more complex. Organic products and ingredients are often
handled by dozens of operations, including uncertified entities, on
their way to the consumer. A robust system of traceability and fraud
prevention can help reduce the risks of complex supply chains and
minimize fraud.
---------------------------------------------------------------------------
\55\ A credence good is something with value or qualities that
cannot be easily determined by the consumer before, or even after,
purchase.
---------------------------------------------------------------------------
The length and complexity of modern supply chains present many
risks to organic integrity. Activities that can compromise organic
integrity and void the use of the USDA organic label include physical
risks such as contact with substances prohibited in organic production
(e.g., pesticides, fumigants, or cleaning agents) and mixing or
commingling of organic and nonorganic products. Integrity can also be
compromised if a nonorganic product is mistakenly labeled or identified
as organic, or if poor recordkeeping cannot demonstrate that a product
was produced on a certified farm and handled according to the organic
regulations. Additionally, fraud can occur through falsification of
records and labeling to claim that a nonorganic product is certified
organic. Breach of integrity can occur at any point in a supply chain,
from production to final sale. In addition, the prevalence in organic
supply chains of uncertified operations, who do not have direct USDA or
certifying agent oversight, increases the chance that loss of integrity
may occur and/or go unreported.
Organic products therefore require additional care to verify
organic status and ensure that products bought and sold are genuinely
organic and have not been compromised. Because full visibility across
an entire supply chain is difficult, this rule focuses on using
critical information at control points where risk is highest to verify
chain of custody and confirm organic integrity. This is primarily done
by building a record of product transaction and movement that
demonstrates proper handling and maintenance of integrity. Without a
verified transaction record, operations (and by extension, consumers)
don't have a full picture of a product's history, and breaches of
integrity can go unnoticed, allowing compromised product to continue
along a supply chain to the consumer.
The current USDA organic regulations require general recordkeeping
and verification of organic integrity, but the requirements are not
specific and lack key types of information and practices that are
necessary to prove the integrity of products from long, complex supply
chains. This lack of recordkeeping information often leads to
incomplete audit trails, and operations and
[[Page 3602]]
certifying agents are often unable to verify product origin or organic
integrity. The specific recordkeeping, auditing, and fraud prevention
procedures in this rule will augment existing practice to ensure more
complete visibility into organic supply chains. This visibility will
allow operations and certifying agents to complete more rigorous
verification of organic products and identify and stop loss of organic
integrity before it moves further into organic supply chains.
All successful systems of traceability include three common
elements: (1) traceability within a single operation; (2) traceability
one step forward and one step back from an operation in a supply chain;
and (3) bidirectional traceability along a supply chain by a third
party. This rulemaking supports traceability by clarifying who is
responsible for each element: certified organic operations are
responsible for traceability within their operation, back to their
suppliers, and forward to their customers; certifying agents are
responsible for verifying and tracing products along a supply chain and
assessing a certified operation's system of traceability.
Fraud is also a significant risk to organic integrity; this
rulemaking therefore focuses effort on its prevention. To clarify what
this means, Sec. 205.2 of the organic regulations includes a
definition of organic fraud: deceptive representation, sale, or
labeling of nonorganic products as ``100 percent organic,''
``organic,'' or ``made with organic (specified ingredients or food
group(s)).'' This broad definition helps clarify portions of this
rulemaking's policy (e.g., Sec. Sec. 205.201(a)(3) and 205.504(b)(7)),
but is not intended to be used as a mechanism or criterion for
enforcement.
Certified Operations
Recordkeeping
Section 205.103 of the organic regulations describes the
recordkeeping responsibilities of certified operations. Records are
used by operations, certifying agents, the USDA, and others to verify
the compliance of organic operations and products. Clear and auditable
records also support traceability. This rulemaking clarifies
recordkeeping requirements to support the traceability of organic
products both within and between operations.
General Recordkeeping Requirements
Section 205.103(b)(2) specifies that a certified operation's
records must describe all activities and transactions of the operation.
This includes physical and financial possession, production, handling,
title, and contractual oversight responsibilities of the organic
products and ingredients the operation produces or handles. Such
records must span the time of purchase or acquisition, through
production, to sale or transport. This requirement supports
``internal'' traceability, or the ability to track the movement,
handling, and organic status of products within a single operation.
These records are needed to verify the compliance of an organic
operation and its products, and supports on-site inspections by
providing information for mass-balance audits and traceability
verification by certifying agents (see Sec. 205.403(d)(4)-(5)).
Section 205.103(b)(2) also requires that an operation's records
must be sufficient to trace products back through a supply chain to the
last certified operation. Keeping ``external'' records back to the last
certified operation is needed to verify the source of organic products.
Note that records must reach back to the last certified operation.
Operations receiving organic products from uncertified suppliers (e.g.,
an exempt wholesaler) must keep records demonstrating how the
uncertified operation maintained organic product integrity. This may
require keeping records from several uncertified operations in
sequence; in all cases the records must show an audit trail back to the
last certified operation. Operations can demonstrate an audit trail by
using various types of documentation that are typically used during
sale, purchase, and transfer, such as receipts, invoices, shipping or
receiving manifests, shipping logs, bills of lading, or transaction
certificates. The organic industry creates and transfers this
documentation (almost always electronically) in the usual course of
business, and sales contracts often list this documentation as a
condition of the sale. Typically, handling entities along a supply
chain (such as a transporter, broker, or storage facility) will send
electronic documentation directly to the buyer either before or at
receipt of a product. A buyer may also obtain additional documents or
records directly from the certified operation that sold the product.
Maintaining records back to the last certified operation will
support supplier verification and fraud prevention plans (Sec.
205.201(a)(3)). Such records will also ensure certifying agents have
the information they need to verify the compliance of products during
on-site inspections (Sec. 205.403(d)(5)) and during supply chain
traceability audits (Sec. 205.501(a)(21)).
Section 205.103(b)(2) describes a certified operation's minimum
recordkeeping requirements. Certified operations may need to keep
additional records beyond the scope of Sec. 205.103(b)(2) to comply
with other portions of the organic regulations and the Act. For
example, to comply with Sec. 205.236, Origin of livestock, livestock
operations must maintain records demonstrating that animals were
organically managed from the last third of gestation, which may include
place and date of birth. This may require records that trace purchased
animals back to the operation where the animal was born to prove origin
and organic management (i.e., the records must trace beyond the last
certified operation to prove compliance).
Audit Trail Documentation
Certified operations must keep audit trail documentation for all
organic products they produce or handle. Audit trail documents are
records used to determine the source, transfer of ownership, and
transportation of organic products (see definition of audit trail in
Sec. 205.2). For the purpose of audit trail documentation, the
``source'' of organic products is the certified operation that supplied
the product to the operation. Examples of audit trail documentation may
include but are not limited to receipts, invoices, shipping or
receiving manifests, shipping logs, bills of lading, and transaction
certificates. Audit trails must document the history of organic
products back to the last certified operation (per Sec.
205.103(b)(2)).
Audit trail documentation must identify organic products as ``100%
organic,'' ``organic,'' or ``made with organic (specified ingredients
or food group(s)),'' as appropriate. Operations may use abbreviations
or acronyms to identify products, provided that the abbreviations or
acronyms are easily understood. Certified operations should consider
describing use of any abbreviations or acronyms in their OSP; this will
facilitate on-site inspections and record audits by certifying agents,
and help ensure that records are ``readily understood and audited''
(Sec. 205.103(b)(2)).
Explicit identification of products as organic is required for
audit trail records (i.e., ``transaction'' or ``external'' records).
``Internal'' records do not need to provide explicit organic
identification (e.g., ``100 percent organic''). However, all systems of
records must be ``in sufficient detail as to be readily understood and
audited'' to meet the requirements of Sec. 205.103(b)(2). This means
that operations must be able to identify products they produce or
[[Page 3603]]
handle as organic, even if records do not explicitly state ``organic.''
For example, an operation may use an inventory management system that
uses lot codes, batch numbers, or other designation system that
indicates organic status. Such designation systems must be clear and
auditable to facilitate on-site inspection and verification of
compliance.
Audit trail documentation that clearly identifies organic products
will support an operation's verification of suppliers and
implementation of fraud prevention plans. They will also allow
certifying agents to verify compliance of suppliers and products during
on-site inspections (Sec. 205.403(d)(5)) and supply chain traceability
audits (Sec. 205.501(a)(21)).
Fraud Prevention Plans
Section 205.201(a)(3) requires all certified operations to maintain
and implement practices to verify the organic status of suppliers and
products in their supply chain and to prevent organic fraud. Often
called ``fraud prevention plans,'' these procedures and practices
support early detection, prevention, and mitigation of fraud, and
strengthen integrity across organic supply chains.
A fraud prevention plan must be included in an operation's OSP.
This allows certifying agents to assess the effectiveness of certified
operations' anti-fraud practices and compliance with the organic
regulations. A fraud prevention plan must be appropriate to the
activities, scope, and complexity of the operation, and should be
sufficient to address the verification and anti-fraud needs of the
particular operation. This means not all fraud prevention plans will be
alike. For example, a producer who does not handle another operation's
organic products may develop a simple fraud prevention that verifies
purchased inputs comply with organic regulation. In contrast, a
processor that receives many organic ingredients from numerous
suppliers should develop a fraud prevention plan that describes
practices to detect, prevent, minimize, and mitigate organic fraud
risks in lengthy supply chains.
Because fraud prevention plans must verify the organic status of
suppliers and organic products, they should include a description of
how an operation verifies organic status back to the last certified
operation in the supply chain. This supports recordkeeping and audit
trail requirements at Sec. 205.103(b)(2) and (3) and allows certifying
agents to verify compliance during on-site inspections and supply chain
traceability audits.
As a best practice, a robust plan for supply chain oversight and
organic fraud prevention may include:
A map or inventory of the operation's supply chain that
identifies suppliers;
Identification of critical control points in the supply
chain where organic fraud or loss of organic status are most likely to
occur;
A vulnerability assessment to identify weaknesses in the
operation's practices and supply chain;
Practices for verifying the organic status of any product
they acquire and/or use;
A process to verify suppliers and minimize supplier risk
to organic integrity;
Mitigation measures to correct vulnerabilities and
minimize risks;
Monitoring practices and verification tools to assess the
effectiveness of mitigation measures; and
A process for reporting suspected organic fraud to
certifying agents and the NOP.
Certifying Agents
Supply Chain Traceability Audits
Traceability of organic products across multiple operations in a
supply chain is an effective strategy to detect fraud, conduct
investigations, and verify compliance of products and operations.
Therefore, Sec. 205.501(a)(21) of the organic regulations requires
certifying agents to conduct risk-based supply chain traceability
audits of products and operations they certify.
What is a supply chain traceability audit?
A supply chain traceability audit (SCT audit) is the process of
identifying and tracking the movement, sale, custody, handling, and
organic status of a product along a supply chain. The objective of a
supply chain audit is to verify a product's compliance with the organic
regulations. SCT audits can be used to investigate evidence or
suspicion of fraud, verify compliance of high-risk products,
investigate patterns of activity, trace the source of products
contaminated with prohibited substances, surveil high-risk supply
chains, or for other compliance-related reasons.
Criteria and Procedures for Supply Chain Traceability Audits
Certifying agents must maintain criteria and procedures that
describe the use of risk-based SCT audits. This must include (1)
criteria used to identify high-risk operations and products for SCT
audits, and (2) procedures used to conduct SCT audits. SCT audits
conducted by the certifying agent must be based on these criteria and
procedures. To ensure that AMS is made aware of organic fraud when it
is discovered, certifying agents must also maintain procedures to
report credible evidence of fraud to the USDA. Copies of these
procedures and criteria should be kept by the certifying agent to
demonstrate its expertise and ability (Sec. 205.504(b)(7)); this
allows AMS to review and evaluate use of SCT audits during regular
accreditation audits.
SCT audits should be initiated by events or criteria chosen and
described by the certifying agent. For example, SCT audits may be
initiated to investigate evidence or suspicion of fraud, verify
compliance of an organic product, investigate patterns of activity,
trace the source of positive residue testing, surveil high-risk supply
chains or products, or to address any other compliance-related risk,
activity, or need identified by the certifying agent.
Use of Supply Chain Traceability Audits
The length, extent, and frequency of an SCT audit may vary and
should be determined by the objective of the audit (i.e., an SCT audit
ends when its objective is achieved). SCT audits may trace back to the
origin (production site) of a product, or until a noncompliance is
verified or cleared. For example, if a certifying agent's objective is
to verify the production origin of an ingredient, the SCT audit should
trace the ingredient through the entire supply chain to the farm or
ranch where the ingredient was produced. In contrast, if an SCT audit
is initiated to determine the source of a positive residue test, the
SCT audit may conclude when the source of the contamination is
identified (which may only be several ``steps'' back in the supply
chain).
The number, frequency, type, and extent of SCT audits should be
appropriate to the number, scope, and complexity of operations the
certifying agent certifies.
Information Sharing
To facilitate supply chain traceability audits, investigations, and
verification of organic status, AMS requires certifying agents share
compliance- and enforcement-related information with each other. Per
Sec. 205.501(a)(10), certifying agents must maintain strict
confidentiality with respect to its clients and not disclose business-
related information to third parties that are not involved in the
regulation or certification of operations, as required by the OFPA (7
U.S.C. 6515(f)).
[[Page 3604]]
Certifying agents must exchange information that is credibly needed
to determine an operation's compliance with the USDA organic
regulations, including assessment of applications for certification,
noncompliance investigations, suspension/revocation of certification,
supply chain traceability audits, verification of audit trail
documentation, and verification of the organic status of products
represented as organic (see Sec. 205.501(a)(10)(ii) and (a)(13)).
Section 205.501(a)(10)(iii) requires that compliance-related
proprietary business information exchanged between certifying agents
must remain proprietary, and that all certifying agents involved in the
exchange must preserve the confidentiality of the information during
and after the exchange. Certifying agents must maintain copies of the
procedures used to exchange information and maintain confidentiality of
information (Sec. 205.504(b)(4)). These requirements will ensure
confidentiality of information during compliance activities that span
multiple certified operations and certifying agents, such as supply
chain traceability audits and investigations.
Conclusion
The traceability and fraud prevention requirements discussed above
are part of a holistic organic control system that enhances the
oversight, enforcement, and integrity of organic products. Many other
sections of this rule support and facilitate traceability and fraud
prevention; stakeholders should read the following sections to better
understand how to implement this rule's traceability and fraud
prevention requirements:
Section III. A: Applicability and Exemptions from
Certification;
Section III. B: Imports to the United States;
Section III. C: Labeling of Nonretail Containers;
Section III. D: On-Site Inspections;
Section III. G: Paperwork Submissions to the
Administrator; and
Section III. H: Personnel Training and Qualifications.
Summary of Changes to the Final Rule
AMS made several changes to the proposed regulatory text when
writing this final rule. Changes to the proposed rule are discussed
below and are followed by responses to specific themes from public
comment:
AMS revised the definition of organic fraud to remove
``intentional'' and ``for illicit economic gain.'' ``Intentional'' is
not needed because this defined term is not used for enforcement; it is
used to help explain the objective of this rulemaking and many of its
provisions. AMS removed the phrase ``for illicit economic gain''
because not all fraud results in or is motivated by economic gain. The
final defined term is more flexible than proposed and encompasses a
broader range of potential fraud types.
AMS added the new term supply chain traceability audit. A
similar definition was used in the preamble of the proposed rule to
help stakeholders understand the rule and its objectives. AMS added
this new term to more formally clarify its purpose and objective, and
to more clearly define the expectations of traceability audits by
certifying agents (see Sec. 205.501(a)(21)).
AMS removed the requirement in Sec. 205.103(b)(2) to
identify specific labeling categories (e.g., ``100% organic'') in
records. Removing this requirement avoids the potential for additional
recordkeeping burden that some comments noted the proposed rule could
unintentionally create, and gives operations more flexibility in how
they keep records.
AMS specified the scope of recordkeeping in Sec.
205.103(b)(2) to more clearly indicate the types of records that
operations should keep, and what timeframe they should span. This
presents clear expectations that support traceability and verification
of organic products, but also puts clear boundaries on the scope of
records to control burden and cost to operations.
AMS added a requirement to identify organic status (e.g.,
``100 organic'') in audit trail documentation at Sec. 205.103(b)(3)
and added ``or similar terms, as applicable.'' The proposed rule had
included this at (b)(2) as a general requirement for all records; the
rulemaking only requires such identification on audit trail
documentation (see audit trail at Sec. 205.2). This change will avoid
the potential for additional recordkeeping burden that some comments
noted the proposed rule could unintentionally create, but still ensures
that this critical information is available to trace organic products
between operations and to verify integrity.
AMS revised Sec. 205.201(a)(3) to clarify that fraud
prevention plans must be appropriate to an operation's activities,
scope, and complexity. This change responds to public comments that
were concerned about disproportionate burden (i.e., greater cost) on
small operations, especially small producers. This change may allow
operations with less complex activities and/or a more limited scope to
write and implement simpler fraud prevention plans.
AMS removed ``back to the source'' in Sec. 205.501(a)(21)
because public comments indicated this phrase was unclear and that the
length of supply chain traceability audits varies. The new term supply
chain traceability audit states the objective of such an audit--to
verify an organic product's compliance--and therefore serves to clarify
that the length and extent of supply chain traceability audits will
vary depending on the objective and findings of the process.
In Sec. 205.501(a)(15), AMS added references to Sec.
205.504(b)(7) and Sec. 205.501(a)(13). This more clearly specifies
that certifying agents are to use their own criteria for identifying
high-risk operations and conducting supply chain traceability audits,
and that they are to share information with other certifying agents to
conduct audits and verify compliance.
AMS added the term supply chain traceability audit to
Sec. 205.504(b)(7) to more clearly state the need for and objectives
of the risk criteria and procedures in this paragraph.
AMS did not change Sec. 205.501(a)(10), Sec.
205.501(a)(13), or Sec. 205.504(b)(4).
Summary of Public Comment
The majority of public comments supported AMS's proposed revisions
to recordkeeping requirements for certified operations. Many comments
noted that including a description of full organic status (e.g., ``100
percent organic . . .'') on all records may be burdensome and suggested
that AMS allow the use of abbreviations, acronyms, or shorthand when
identifying organic ingredients. Other comments asked for additional
clarity about the definition of audit trail and what types of
documentation are needed to meet the requirements of Sec.
205.103(b)(3). Finally, a few comments claimed that keeping full
organic identification on all records may be burdensome and asked that
AMS not finalize this requirement in cases where inventory management
systems can indicate organic status via lot codes or batch numbers.
Comments largely supported AMS's proposed use of fraud prevention
plans by certified operations. However, many comments requested
additional specificity about what should be included in fraud
prevention plans. Other comments noted that fraud prevention plans may
be difficult for very small businesses to write and implement and
recommended AMS develop templates, examples, and
[[Page 3605]]
generic forms for small operations to use.
AMS received many comments about the proposed definition of organic
fraud. Some comments requested that AMS remove ``illicit'' and from the
definition, arguing that fraud may not always constitute illegal
activity. Others suggested removing ``intentional,'' citing the
difficulty of proving intent. Several comments also suggested AMS
harmonize the proposed definition with existing definitions from other
organizations such as GFSI, the EU, ISO, and FDA.
Public comment generally supported the proposed use of supply chain
traceability audits. Many comments asked AMS to clarify the
requirements of and extent of supply chain traceability audits,
particularly how far back an audit should trace a product. Others
suggested adding a definition of supply chain audit or traceability.
Opinions varied widely on the number of supply chain traceability
audits to be conducted, with many comments suggesting a minimum
percentage of operations or a risk-based selection. Many comments also
discussed the administrative impacts of supply chain traceability
audits: a few comments claimed some certifying agents may not have the
capacity of expertise to conduct audits; others highlighted challenges
with information sharing and coordination among certifying agents. A
few comments expressed a desire for AMS to coordinate supply chain
traceability audits.
Finally, some comments suggested alternatives to AMS's proposed
traceability and fraud prevention strategy, including trusted trader
programs, increased surveillance by AMS, and exemptions for businesses
that already participate in other traceability programs.
Responses to Public Comment
Definition of Organic Fraud
(Comment) Comments asked AMS to use ``willful'' instead of
``intentional'' in the definition of organic fraud.
(Response) The rulemaking does not use ``willful'' or
``intentional'' in the final definition. This allows for a more
flexible definition that encompasses a broader range of potential fraud
types. ``Willful'' and ``intentional'' are not needed because organic
fraud is not used for enforcement; it is used to help explain the
objective of this final rule and many of its provisions.
(Comment) Comments asked AMS to remove ``for illicit economic
gain,'' claiming that not all fraud is illicit or economic in nature.
Comments also asked AMS to harmonize the definition of organic fraud
with terms used by other standards organizations such as ISO, GFSI,
FDA, and the EU.
(Response) Many of the organizations mentioned in public comment
focus on ``economic gain'' as a key factor in defining fraud. The final
rule does not include the phrase ``for illicit economic gain'' because
not all fraud results in or is motivated by economic gain. This
definition is more flexible and encompasses a broader range of
potential fraud types than terms used by other standards organizations.
Recordkeeping
(Comment) Comments requested that the regulatory text explicitly
allow use of abbreviations for indicating organic status on records.
(Response) AMS amended Sec. 205.103(b)(3) to allow use of similar
terms such as acronyms or abbreviations for identifying organic status
on audit trail documentation. Abbreviations or acronyms should be
easily understood to meet the requirement that all records ``be readily
understood and audited'' (Sec. 205.103(b)(2).
(Comment) Comments are concerned that the requirement to identify
organic products as such on all records will add an unnecessary
recordkeeping burden that duplicates existing recordkeeping or
inventory management systems.
(Response) The requirement to identify products as ``100%
organic,'' ``organic,'' or ``made with organic (specified ingredients
or food group(s)),'' has been revised to apply only to audit trail
documentation. Other records should also indicate organic status to
meet the requirement that all records ``be readily understood and
audited'' (Sec. 205.103(b)(2)). However, operations may use a system
of recordkeeping or inventory management system that uses lot codes,
batch numbers, or other designation system that indicates organic
status, as long as such designations are clear and auditable.
(Comment) Commenters requested clarity on the use of ``internal''
vs. ``external'' records for purposes of supply chain traceability.
(Response) The requirements of Sec. 205.103(b)(2) applies to
broadly all records maintained by an operation, including both
``external'' and ``internal'' records. Section 205.103(b)(3) applies
only to audit trail documentation, i.e., ``external'' or
``transaction'' records.
Fraud Prevention Plans
(Comment) Comments asked AMS for more detail about the scope of
fraud prevention plans and what elements should be included in them.
(Response) The preamble of this rulemaking describes best practices
that operations may use to develop and implement fraud prevention
plans. The final regulatory text does not include specific practices or
requirements; this provides maximum flexibility for operations and
certifying agents to determine what is appropriate for individual
operations. A fraud prevention plan must describe the operation's
monitoring practices and procedures they use to verify suppliers,
verify products received, and prevent organic fraud. The plan must be
appropriately tailored to the activities, scope, and complexity of the
operation.
(Comment) Comments stated that the fraud prevention plan
requirement would cause a disproportionate burden (i.e., greater cost)
on small operations, especially small producers.
(Response) The final rule regulatory text and the preamble explain
that an operation's fraud prevention plan must be appropriate to the
operation's complexity, scope, and activities. This may allow
operations with less complex activities and/or a more limited scope to
write and implement simpler fraud prevention plans.
Supply Chain Traceability Audits
(Comment) Comments requested greater clarity about the proposed
rule's use of the terms traceback, mass-balance, and supply chain
audits.
(Response) Verification of traceability back to the last certified
operation and mass-balance audits are routine practice during on-site
inspection of certified operations. Section 205.403(d)(4)-(5) describe
the use of these mechanisms. In contrast, supply chain traceability
audits are triggered by criteria defined by the certifying agent. A
supply chain traceability audit generally encompasses at least a
portion of a supply chain and is conducted to verify the compliance of
a product with the organic regulations and the Act.
``Traceback'' is a term commonly used in the organic industry.
However, this term was used inconsistently in public comment and there
was no clear preference for how to define it. Therefore, AMS has
avoided using this term in the final rule. AMS defines and uses the
term supply chain traceability audit to describe certain activities,
and the regulatory text clarifies the extent of other traceability
requirements (e.g., Sec. 205.103(b)(2)) requires that an operation's
records must be traceable back to the last certified operation).
(Comment) Comments asked AMS for clarification about the phrase
``back to
[[Page 3606]]
the source'' in the proposed rule's revision to Sec. 205.501(a)(21).
(Response) This phrase is not used in the SOE final rule. The
length and extent of supply chain traceability audits will vary
depending on the objective and findings of the process. Some supply
chain traceability audits may extend back to the site of production,
while others may only go a few steps back in a supply chain; the audit
ends when its objective (e.g., verification of compliance) is achieved.
(Comment) Many comments discussed the administrative impacts of
supply chain traceability audits: a few comments claimed some
certifying agents may not have the capacity or expertise to conduct
audits; others highlighted challenges with information sharing and
coordination among certifying agents.
(Response) Supply chain audits are an important tool for oversight
in the organic market. AMS has added flexibility for certifying agents
to define the conditions for when supply chain audits are necessary.
Further, there are other requirements in this rule that will support
supply chain audits: certification of additional handlers in supply
chains, mandatory NOP Import Certificates, identifying organic products
on audit trail documentation, and information sharing among certifying
agents.
Q. Technical Corrections
The table below includes the regulatory text related to this
section of the rule. A discussion of the policy follows.
----------------------------------------------------------------------------------------------------------------
Section Final regulatory text
----------------------------------------------------------------------------------------------------------------
205.301............................................. Product composition.
Paragraphs (f)(2) and (3).
205.400............................................. General requirements for certification.
Paragraph (b).
205.401............................................. Application for certification.
Paragraph (a).
----------------------------------------------------------------------------------------------------------------
AMS has revised Sec. 205.301 to correct a technical error in the
description of the prohibition of ionizing radiation and sewage sludge.
A previous technical correction (80 FR 6429) contained an error in the
language used to describe the prohibition on ionizing radiation and
sewage sludge. The terms ``produced'' and ``processed'' were
erroneously used to describe the use of ionizing radiation and sewage
sludge, respectively, in the current regulatory text. This action
corrects the language at paragraphs (f)(2) and (f)(3) to clarify that
all products labeled as ``100% organic'' or ``organic'' and all
ingredients identified as organic in the ingredient statement of any
product must not be processed using ionizing radiation or produced
using sewage sludge.
AMS also revised Sec. Sec. 205.400(b) and 205.401(a) to correct
the references to organic system plans (Sec. 205.201), which was
incorrectly cited in the previous organic regulation.
R. Additional Amendments Considered But Not Included in This Rule
The Strengthening Organic Enforcement proposed rule asked the
public for feedback on two additional subjects: packaged product
labeling and expiration of certification. AMS did not propose amending
the portions of the USDA organic regulations that relate to these
subjects. The specific questions asked in the proposed rule were meant
to elicit feedback from stakeholders about the two topics for possible
future consideration. AMS has summarized the public comment received
below.
Summary of Public Comments: Packaged Product Labeling
Processed and/or packaged food products are often manufactured or
packaged by one business and labeled for sale/distribution by another
business. This type of relationship, sometimes called contract
manufacturing and private labeling, is common in both the organic and
nonorganic markets. This rulemaking does not change how such products
are labeled for retail sale. However, in the proposed rule AMS asked
for public comment on private-labeled product labeling, prompting
feedback about preferred terminology and which businesses should be
listed on labels.
Overall, there was no consensus among comments about issues of
organic private-labeled products, including who should be certified,
what terminology to use, and which operations and certifying agents
should be listed on labels. Because private label and brand/contract
relationships are on a contract-by-contract basis to protect
proprietary information, some comments argued that creating a single
set of rules to govern these relationships may change how private
labels operate in the future. The comments received reflect this, and
include a variety of opinions based on a commenter's position in the
organic supply chain. Responses from public comments are summarized
below along with background information to provide context and help
explain comments.
Preferred Terminology To Describe Private Label Products and Parties
Throughout the supply chain there are many steps where brand
companies can leverage contracted companies to produce items for sale
under the brand. After raw material sourcing, there are opportunities
for a company to contract out steps such as manufacturing, packaging,
and distribution.
Because of the variable use and function of contracted
organizations in organic production, it is important to use common
terminology to refer to organic operations and their certifying agents.
Many comments requested consistent regulatory terminology to categorize
these operations in relation to the organic supply chain, but there was
no clear preference for certain terminology. Terms and relationships
between contract food producers and brand owners are highly variable in
the organic industry, but comments highlighted opportunities to align
with commonly used and understood terminology. Comments suggested terms
that could be consistently used to prevent confusion about which
companies should appear on product labels, including contract
manufacturer or ``co-man,'' contract packer or ``co-packer,'' external
distributors, Private label entities/owners, and brand owners.''
Listing Contract Manufacturers on Labels
The SOE proposed rule asked the public if private label products or
brands that use contract manufacturers should list those manufacturers
on the product label. The majority of
[[Page 3607]]
comments supported optionally listing contract manufacturers. Those who
did not agree with this opinion requested that products should list the
brand name and the contract manufacturer. Currently, it is mandatory
for some product categories such as meat, poultry, and dairy to have an
Establishment Number that can trace back to the facility where it was
processed. For other products that are not currently mandated to
provide this information, identity of the contract manufacturer is
often considered proprietary information, and in some instances, there
could be multiple contract manufacturers operating at the direction of
one brand owner.
Commenters were concerned that listing contract manufacturers would
result in a loss of competitiveness; mandatory listings would expose
proprietary information and undercut the success of these
relationships. For brand owners that use several contracted companies,
their products would need multiple versions of labels and traceability
would become more complex. Comments also questioned the purpose of
listing contract manufacturers on labels, some arguing that it would
not improve organic integrity or traceability, especially because
certifying agents are already listed on products. Some comments
discussed that certifying agent information is enough to trace the
product back to the manufacturer, making the listing of contract
manufacturers unnecessary.
Listing Certified Operations on Private-Label Packaged Products
The organic regulations currently require listing a certified
operation on branded products. The proposed rule asked commenters which
certified operations should be added to the packaging of private label
products, in the interest of furthering traceability. Many comments
recommend the brand owner/distributor and their certifying agent be
listed on retail labels, with some comments stating no preference. Some
commenters stated listing the brand owner would require companies to
impose traceability standards on the contract companies they use.
Some individuals recommend listing the last certified operation in
the supply chain, to improve clarity and traceability, while others
contradict this point by discussing the confidentiality concerns of
listing the contract manufacturer. Commenters noted that distributors
may be the best certified operation to list because they are often the
last step in the organic handling process and can trace a product back
through manufacturing and sourcing. Conversely, others noted that not
all companies handle distribution internally (choosing instead to use a
contracted company).
Other comments claim that listing co-packers on labels is not
necessary if brand owners are certified; however, some comments
indicated it is unclear if brand owners need to be certified. Finally,
a few comments recommended AMS assess the labeling requirements'
alignment with the FDA.
Listing Certifying Agents on Private-Label Packaged Products
Multiple certifying agents are typically involved in the production
and processing of organic products (from raw materials to material
refining, manufacturing, and distribution); each assures that an
individual process or step meets the organic standard. In the case of
brand companies with contract manufacturers, comments did not clearly
agree on which certifying agent (that of the brand company or that of
the contract manufacturer) to list on the product label. Many
individuals supported listing the certifying agent of the brand owner/
distributor, but the brand owner may not be certified. For example,
some comments pointed out that retailers are often the brand owners/
distributors of organic products, but they are often exempt from
organic certification. In this case, some commenters recommended
listing the contract manufacturer's certifying agent.
Others recommended listing the certifying agent that certified that
last handling operation in the supply chain, arguing that this would
aid traceability. However, due to the variety of different
manufacturing/branding relationships, this could be either the
certifying agent of the brand owner or the manufacturer.
Matching the Certifying Agent to the Listed Operation
Organic product labels currently must include both a certifying
agent and an operation. Commenters generally agreed that if a specific
operation is listed (i.e., contract manufacturer), that the certifying
agent on the label should match. Comments explained that matching the
two organizations would make it easier to contact a responsible party
or file a complaint. Commenters on the proposed rule also agree that a
label that lists the brand name next to the contract manufacturer's
certifying agent would be confusing. However, given that some brand
owners may not be certified, commenters noted this mismatch may already
be happening in the marketplace.
Summary of Public Comments: Expiration of Certification
Under current USDA regulation, organic certification continues
until surrendered, revoked, or suspended (Sec. 205.404(c)). Certified
operations must undergo an annual recertification process (Sec.
205.406), but certification does not expire after one year. While
developing the SOE proposed rule, AMS considered, but did not propose,
adding a mechanism where certification would expire if an operation did
not complete the annual recertification process timely.
The proposed rule included specific questions about expiration of
certification and asked the public to comment on the subject. At this
time, AMS has chosen not to pursue a policy of expiration of
certification. The following is a summary of public comments received
in response to the questions AMS asked the public in the SOE proposed
rule.
Potential Improvements to Organic Integrity
The SOE proposed rule asked the public how annual expiration of
certification could improve organic integrity. Some comments suggested
that expiration could be an incentive for operations to punctually
renew. Some comments adverted that it may help address the common
incident of adverse action circumstances by encouraging operations to
update their (organic system plan) OSP and pay fees on time. Commenters
expressed if operations understood the annual expiration date,
operations with unresolved noncompliances would risk losing
certification via expiration. Those who did not agree indicated that
current regulation specifies that operations are certified unless
suspended or revoked. The annual expiration would disrupt this current
system of recertification.
Limitations of Expiration of Certification
The proposed rule requested the public to comment on what the
limitations of requiring expiration of certification may be. Commenters
forecast potential negative effects such as marketplace disruption,
communication burdens and administrative burdens. Commentators
mentioned that expiration may negatively impact the status of inventory
of operations who allowed their certification to expire. One remark
stated that the requirement could place additional administrative
burden on the certifying agent: expiration of certification would
result in the
[[Page 3608]]
certifying agent having to update systems, train staff, educate
operations on the policy change, and frequently remind operations of
the upcoming expiration date.
Minimum Requirement for Renewing Certification
The SOE proposed rule asked for comments on what the minimum
requirement for renewing certification should be. Many commenters
recommended the following process: submit required paperwork, pay
annual fee, and confirm interest in renewing. It was also recommended
that on-site inspection should not be a requirement for
recertification.
Operations With Adverse Actions
The proposed rule asked the public if an operation with adverse
actions that are in the appeals process could renew certification.
Comments expressed contrasting views on this matter, some finding that
operations should be able to renew, and some communicating that those
operations should not have the flexibility to renew their
certification. Some comments pointed out that the appeal process for a
proposed suspension is lengthy, and that not allowing an operation with
pending adverse actions to renew certification would promptly remove
them from the system and prevent potentially noncompliant product from
entering the market. Some individuals stated that depending on the
severity of the pending adverse action, AMS should administer a system
that would not block an operation from renewing its certification due
to minor non-compliances. Others asked that if an operation has a
record of failing to address certain adverse actions, then the system
should prevent them from renewing their certification.
Grace Period for Renewing Certification
The SOE proposed rule asked commenters if a grace period would be
appropriate for operations that failed to renew by the expiration date.
Commenters were also asked what the length of the grace period should
be. Overall, comments proffered a 30- or 90-day grace period or
mentioned that the current system already has a grace period built into
the timeline. Some individuals suggested that a grace period would
improve assurance among farmers.
Process of Regaining Certification
The SOE proposed rule asked the public to express their opinion on
what process should exist for an operation to regain organic
certification should they allow it to expire. Many individuals
communicated that the process of regaining an expired certification
should be different than regaining a suspended/revoked certification.
They stated the process should also be dependent on the presence and
severity of adverse actions and there should be leniency within the
duration. Some commentators proposed that operations with expired
certification should apply as a new applicant, unless applying within
the grace period. However, a commenter identified a potential loophole
in tracking pending adverse actions of operations with expired
certification; they recommended a system that would keep a record of
operations with any pending adverse actions.
Notification of Upcoming Expiration of Certification
The SOE proposed rule asked the public if certified agents should
notify certified operations of their upcoming expiration of
certification. Commenters clarified that notifying certified operations
is currently a widespread practice. Moreover, a commenter suggested
that notification should be sent from the Organic Integrity Database,
which may normalize the process.
IV. Regulatory Analyses
A. Summary of Economic Analyses
Executive Orders 12866 and 13563 control regulatory review.\56\
Executive Orders 12866 and 13563 direct agencies to assess all costs
and benefits of available regulatory alternatives, and, if regulation
is necessary, to select regulatory approaches that maximize net
benefits (including potential economic, environmental, public health
and safety effects, distributive impacts, and equity). Executive Order
13563 emphasizes the importance of quantifying both costs and benefits,
reducing costs, harmonizing rules, and promoting flexibility.
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\56\ Executive Order 12866, Regulatory Planning and Review,
September 30, 1993: https://www.archives.gov/files/federal-register/executive-orders/pdf/12866.pdf.
Executive Order 13563, Improving Regulation and Regulatory
Review: https://www.federalregister.gov/documents/2011/01/21/2011-1385/improving-regulation-and-regulatory-review.
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The Regulatory Flexibility Act (5 U.S.C. 601-612) requires agencies
to consider the economic impact of each rule on small entities and
evaluate alternatives that would accomplish the objectives of the rule
without unduly burdening small entities or erecting barriers that would
restrict their ability to compete in the market.
This rulemaking amends amending several portions of the USDA
organic regulations (7 CFR part 205) to strengthen oversight and
enforcement of the production, handling, sale, and marketing of organic
agricultural products in the United States. The amendments address gaps
in the organic standards to deter organic fraud and create a level
playing field for farms and businesses. This reinforces the value of
the organic label by assuring consumers and stakeholders that organic
products meet a robust and consistent standard.
The revised organic standards in this rule affect: certifying
agents; certified operations (farms, processers, and handlers); and
certain operations that are currently excluded or exempt from organic
certification (e.g., certain brokers, traders, importers, exporters).
The following discussion summarizes the economic analysis AMS
performed to estimate the impacts of this rule. A complete economic
analysis of this rulemaking is available at https://www.regulations.gov/. You can access the economic analysis by searching
for document number AMS-NOP-17-0065.
B. Regulatory Impact Analysis
The costs of this rule are primarily due to new or additional
reporting and recordkeeping (paperwork) activities. In addition, there
is cost for some currently excluded and exempt operations to become
certified to handle organic products. AMS estimated the benefits of
this rule by quantifying the organic fraud that will be prevented by
implementation of the rule. The estimated benefits are expected to
outweigh the estimated costs. Total estimated costs and benefits of the
rule are summarized below.
[[Page 3609]]
Costs and Benefits of Rulemaking Discounted at 3% and 7%
----------------------------------------------------------------------------------------------------------------
Average annual cost \a\ Total cost \b\
---------------------------------------------------------------
Amendments 3% Discount 7% Discount 3% Discount 7% Discount
rate rate rate rate
----------------------------------------------------------------------------------------------------------------
Domestic Certifying Agents
----------------------------------------------------------------------------------------------------------------
Imports to the United States.................... $50,247 $37,534 $753,710 $563,016
Certificates of Org. Operation & Cont. of 22,742 21,892 341,130 328,377
Certification..................................
Personnel Training & Qualifications............. 144,661 108,061 2,169,922 1,620,918
On-Site Inspections............................. 96,402 72,012 1,446,031 1,080,176
Supply Chain Traceability & Organic Fraud 4,089 3,054 61,333 45,815
Prevention.....................................
Mediation....................................... 139 134 2,091 2,013
----------------------------------------------------------------------------------------------------------------
Domestic Excluded Handlers
----------------------------------------------------------------------------------------------------------------
Applicability and Exemptions.................... 8,349,390 6,236,939 125,240,844 93,554,079
Imports to the United States.................... 369,807 276,243 5,547,100 4,143,647
----------------------------------------------------------------------------------------------------------------
Domestic Certified Operations
----------------------------------------------------------------------------------------------------------------
Labeling of Nonretail Containers................ 901,966 673,763 13,529,496 10,106,444
Supply Chain Traceability & Organic Fraud 609,066 454,968 9,135,993 6,824,526
Prevention.....................................
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Total Costs and Benefits, Discounted Over 15 Years
----------------------------------------------------------------------------------------------------------------
Total Expected Domestic Costs............... 10,548,510 7,884,601 158,227,651 118,269,011
Total Expected Foreign \c\ Costs............ 8,769,681 6,550,892 131,545,210 98,263,398
Total Expected Domestic & Foreign Costs..... 19,318,191 14,435,494 289,772,861 216,532,409
Total Expected Benefit of Rulemaking........ 32,944,811 24,272,099 494,172,179 364,081,491
----------------------------------------------------------------------------------------------------------------
\a\ These are the estimated annual averages of the 15-year Net Present Value domestic costs discounted at 3 and
7 percent.
\b\ These are the estimated total domestic costs for affected industry in Net Present Value of the stream of
future costs, discounted at 3 and 7 percent.
\c\ AMS assumes all foreign costs will pass through to U.S. consumers and therefore includes these costs in the
final rule. See the full Regulatory Impact Analysis for more detail.
Estimation of Benefits
AMS expects that this rule will reduce organic fraud in the U.S.
market. Therefore, AMS quantified the estimated benefits of the
rulemaking as the value of the projected reduction in organic fraud in
the U.S. organic marketplace following implementation. AMS reviewed
economic studies that identify and quantify fraudulent activity in
retail food markets. AMS then used these estimates of fraud as a
benchmark to quantify the benefits of the rulemaking.
Based on analysis of these food fraud studies, AMS estimated that 2
percent of organic products sold in the United States are currently
subject to some form of fraud. This estimate aligns with rates of food
fraud reported in multiple studies. Therefore, AMS estimated the total
value of organic fraud in the United States as 2 percent of the total
annual organic premiums for domestic organic production and organic
imports, or approximately $109 million annually. AMS chose to use
organic premiums (the cost difference between organic and nonorganic
products) to estimate fraud because this more accurately measures the
value lost to fraud than total sales value (i.e., a fraudulent organic
product only loses the value of its organic attributes, not its entire
value as a food product).
AMS expects the changes from this rule will reduce the amount of
organic fraud (estimated at $109 million annually) by half (an
estimated $54 million). However, it is unclear what proportion of this
$54-million fraud reduction translates directly into social welfare
loss. For example, some certified operations and other compliant
entities in organic supply chains may unknowingly experience some
economic gain from fraud elsewhere in the supply chain. Additionally,
AMS cannot accurately predict how fraud reduction efforts would impact
organic prices, and hence premiums. Given this uncertainty about the
true value of social welfare loss, AMS reduced the estimated $54
million fraud reduction by half for an estimated social welfare gain
(benefit) of $27 million in the first year following implementation of
the rule. Estimated over a 15-year period, and accounting for projected
future annual growth rates of the U.S. organic market, annual benefits
from fraud reduction are estimated to reach $57 million in year 2036.
When discounted over the 15-year period, total economic benefits of the
rulemaking range from $364 to $494 million. When averaged, the economic
benefits range from $24.3 to $32.9 million annually.
Estimation of Costs
The costs of this rule are driven primarily by new or additional
reporting and recordkeeping (paperwork) activities. AMS estimated
additional paperwork cost for each provision of the rule by identifying
the affected population (e.g., number of producers affected by a
change), estimating the time for each affected entity to comply with a
new change, and assigning an appropriate labor category and wage rate.
This accounting of new reporting and recordkeeping costs is discussed
in more detail in the Paperwork Reduction Act section of this
rulemaking.
This rule would also require some currently excluded and exempt
operations to become certified to handle organic products. AMS predicts
that these businesses fall within NAICS categories 425 (Wholesale
Electronic Markets and Agents and Brokers) and 4244 (Grocery and
Related Product Merchant Wholesalers). These categories are very broad
and include mostly businesses that do not handle organic products.
Therefore, AMS used participation rates in the organic sector to
estimate that 1,985 domestic businesses would need to become
[[Page 3610]]
certified organic. Using historic knowledge of certification costs, AMS
estimated that each of the affected 1,985 domestic businesses would
spend $2,000 to become certified organic.
AMS also estimated the cost of this rule to foreign entities,
including both paperwork and recordkeeping burden and costs for certain
businesses to obtain certification. AMS assumes that all foreign costs
will be passed along to U.S. consumers. This may create some tendency
to overstate U.S.-borne costs, as competitive pressures will lead some
compliance costs to be absorbed by businesses and other entities as the
cost of doing business.
Alternatives
AMS also considered three alternatives when developing this
rulemaking.
1. Make no change to the organic regulations. This option would not
implement this rulemaking and leave the organic regulation as-is. AMS
did not select this option because it does not address organic fraud or
other issues affecting organic integrity. AMS considers this a costly
alternative because it forgoes the fraud reduction benefits of the
rulemaking. Regulatory inaction would create social costs that increase
over time. AMS believes the rulemaking will mitigate social welfare
losses by approximately half through the use of practical, risk-based
oversight and enforcement.
2. Require NOP Import Certificates for individual imported
shipments of organic product. The rulemaking will allow NOP Import
Certificates to be issued for multiple shipments over a time span to be
determined at the discretion of each certifying agent. In contrast,
this alternative would require the use of NOP Import Certificates for
each physical shipment of organic products imported into the United
States. AMS found this alternative to be inferior to the rulemaking
because it would create greater cost with limited additional benefit.
AMS believes that the rulemaking's option to issue NOP Import
Certificates on a periodic basis is the most practical, effective, and
cost-sensitive means to address fraudulent imported organic products.
3. Require less-stringent data reporting and training requirements
for certifying agents. AMS also considered a less-stringent alternative
to the rulemaking to assesses if this could lower costs while
maintaining the effectiveness of the rulemaking. Relative to the
rulemaking, this alternative would (1) omit the requirement for
certifying agents to issue standardized certificates of organic
operation generated in the USDA Organic Integrity Database; and (2)
reduce the annual training hours that must be completed by organic
inspectors and certification review personnel. AMS chose not to pursue
this alternative because it would weaken other critical, interdependent
amendments in the rulemaking. AMS predicts any cost reduction of this
alternative would be accompanied by a significant reduction in
effectiveness of the rulemaking.
Regulatory Flexibility Act
AMS also performed additional analysis to determine the rule's
impact to domestic small businesses. This analysis revealed that small
businesses producing, selling, handling, and marketing organic products
would not be adversely affected by the amendments in this rule. AMS
expects that most of the entities affected by this rule are small
businesses as defined by Small Business Administration criteria. For
each category of affected entity (certifying agents, certified
operations, and exempt or excluded operations that need to become
certified), AMS estimates that the costs of the rule for each business
type will be less than one percent of the annual revenue.
A full economic analysis of this rulemaking is available at https://www.regulations.gov/. You can access this rule and the economic
analysis by searching for document number AMS-NOP-17-0065.
C. Executive Order 12988
Executive Order 12988 instructs each executive agency to adhere to
certain requirements in the development of new and revised regulations
in order to avoid unduly burdening the court system. This rule cannot
be applied retroactively. States and local jurisdictions are preempted
under the OFPA from creating programs of accreditation for private
persons or state officials who want to become certifying agents of
organic farms or handling operations. A governing state official would
have to apply to USDA to be accredited as a certifying agent, as
described in section 6514(b) of the OFPA. States are also preempted
under sections 6503 through 6507 of the OFPA from creating
certification programs to certify organic farms or handling operations
unless the state programs have been submitted to, and approved by, the
Secretary as meeting the requirements of the OFPA.
Pursuant to section 6507(b)(2) of the OFPA, a state organic
certification program that has been approved by the Secretary may
contain additional requirements for the production and handling of
agricultural products organically produced in the state and for the
certification of organic farm and handling operations located within
the state under certain circumstances. Such additional requirements
must (a) further the purposes of the OFPA, (b) not be inconsistent with
the OFPA, (c) not be discriminatory toward agricultural commodities
organically produced in other States, and (d) not be effective until
approved by the Secretary.
In addition, pursuant to section 6519(c)(6) of the OFPA, this
rulemaking does not supersede or alter the authority of the Secretary
under the Federal Meat Inspection Act (21 U.S.C. 601-624), the Poultry
Products Inspection Act (21 U.S.C. 451-471), or the Egg Products
Inspection Act (21 U.S.C. 1031-1056), concerning meat, poultry, and egg
products, respectively, nor any of the authorities of the Secretary of
Health and Human Services under the Federal Food, Drug and Cosmetic Act
(21 U.S.C. 301-399), nor the authority of the Administrator of the
Environmental Protection Agency under the Federal Insecticide,
Fungicide and Rodenticide Act (7 U.S.C. 136-136(y)).
OFPA at 7 U.S.C. 6520 provides for the Secretary to establish an
expedited administrative appeals procedure under which persons may
appeal an action of the Secretary, the applicable governing State
official, or a certifying agent under this title that adversely affects
such person or is inconsistent with the organic certification program
established under this title. The OFPA also provides that the U.S.
District Court for the district in which a person is located has
jurisdiction to review the Secretary's decision.
D. Paperwork Reduction Act
In accordance with the Paperwork Reduction Act of 1995 (44 U.S.C.
3501-3520) (PRA), AMS is requesting OMB approval for a new information
collection totaling 368,321 hours for the reporting and recordkeeping
requirements contained in this rulemaking. OMB previously approved
information collection requirements associated with NOP and assigned
OMB control number 0581-0191. AMS intends to merge this new information
collection (0581-0321), upon OMB approval, into the approved 0581-0191
collection. Below, AMS has described and estimated the annual burden
(i.e., the amount of time and cost of labor), for entities to prepare
and maintain information to participate in this voluntary labeling
program. The Organic Foods Production Act of 1990
[[Page 3611]]
(OFPA) provides authority for this action.\57\
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\57\ The Organic Foods Production Act of 1990, 7 U.S.C. 6501-
6524, is the statute from which the Agricultural Marketing Service
derives authority to administer the NOP, and authority to amend the
regulations as described in this rulemaking. This document is
available at: https://uscode.house.gov/view.xhtml?path=/[email protected]/chapter94&edition=prelim.
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Title: National Organic Program.
OMB Control Number: 0581-0321.
Expiration Date of Approval: 3 years from OMB date of approval.
Type of Request: New collection.
Abstract: Information collection and recordkeeping are necessary to
implement reporting and recordkeeping necessitated by amendments to
Sec. Sec. 205.2, 205.100, 205.101, 205.103, 205.201, 205.273, 205.300-
205.302, 205.310, 205.307, 205.310, 205.400, 205.403-205.404, 205.406,
205.500-501, 205.504, 205.511, 205.660-205.663, 205.665, 205.680, and
205.681 of the USDA organic regulations. The rulemaking will protect
organic product integrity and build consumer and industry trust in the
USDA organic label by strengthening organic control systems, improving
organic import oversight, clarifying organic certification standards,
and enhancing farm to market traceability.
This rulemaking amends several sections of the USDA organic
regulations, 7 CFR part 205, to strengthen the NOP's ability to oversee
and enforce the production, handling, marketing, and sale of organic
agricultural products as established by the OFPA. The rule will improve
organic integrity throughout the organic supply chain and benefit
stakeholders at all levels of the organic industry. The amendments will
close gaps in the current regulations to build consistent certification
practices, deter organic fraud, and improve transparency and product
traceability. NOP identified the need for many of the amendments as
part of its direct experience in administering this program,
particularly via complaint investigation and audits of certifying
agents. Other amendments are based on changes to the OFPA included in
the Agriculture Improvement Act of 2018; \58\ the recommendations of a
2017 Office of Inspector General audit; \59\ the recommendations of the
National Organic Standards Board (a federal advisory committee to NOP);
and industry stakeholder feedback.
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\58\ The Agriculture Improvement Act of 2018 (Public Law No:
115-334), commonly known as the ``2018 Farm Bill,'' is available at
https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
Organic certification is discussed in Title X, Section 10104.
\59\ The National Organic Program International Trade
Arrangements and Agreements Audit Report 01601-0001-21, September
2017: https://www.usda.gov/sites/default/files/01601-0001-21.pdf.
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This rulemaking strengthens enforcement with amendments to the USDA
organic regulations and modifies the reporting and recordkeeping
burdens as summarized below.
1. Reduces the types of uncertified handling operations in the
organic supply chain that operate without USDA oversight.\60\ The
amendments require certification of operations that facilitate the sale
or trade of organic products, including but not limited to certain
brokers, importers, and traders. These handlers must obtain organic
certification and develop an organic system plan (OSP) to describe the
practices and procedures used in their operations. Certifying agents
customize the format of the OSP to cover standards applicable to
operations seeking certification. Because traders and brokers do not
farm or manufacture organic products, the OSPs for traders and brokers
will address fewer sections of the organic regulations than OSPs for
operations that farm or manufacture organic products. Therefore,
uncertified traders and brokers will take 40 hours in the first year
after the rule going into effect to prepare an initial OSP. In
subsequent years, AMS estimates each of these entities will incur a
recordkeeping burden of 10 hours annually, and a reporting burden of 20
hours annually, to update their OSP (Sec. Sec. 205.2, 205.100,
205.101, and 205.103).
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\60\ Mandated by the Agriculture Improvement Act of 2018. See
section 10104(a).
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Burden is increased in the rulemaking due to refinements in NAICS
code 425 and the addition of operations from NAICS code 4244 in
response to public comment. The 2018 Farm Bill mandates that NOP reduce
the number of operations excluded from certification at Sec. 205.101.
AMS's revised estimate indicates 1,985 formerly excluded domestic
operations now require organic certification. This includes 855
operations in NAICS code 425 (Wholesale Electronic Markets and Agents
and Brokers) and 1,130 operations in NAICS code 4244 (Grocery and
Related Product Merchant Wholesalers). See the accompanying Regulatory
Impact Analysis (RIA) for more information. AMS assumes the 1,985
domestic excluded operations represent 59 percent of the global total
of excluded handlers (using a benchmark 59 percent to 41 percent ratio
of domestic to foreign operations). Therefore, AMS estimates there are
an additional 1,379 foreign formerly excluded operations, for a total
of 3,364 new handlers that will need organic certification.
2. Requires all currently certified organic operations and new
applicants to describe their procedures for monitoring, verifying, and
demonstrating the organic status of their suppliers and products
received to prevent organic fraud. Operations will include this
information as a supplemental part of the OSP; therefore, AMS allocates
the time to develop these procedures separately from the initial 40
hours to develop an OSP. AMS estimates that each currently certified
operation and applicant seeking certification will need 30 minutes to
describe the supply chain verification procedures and monitoring
practices required by this regulation (Sec. Sec. 205.103 and 205.201).
Burden is increased in the rulemaking due to industry growth.
3. Mandates the use of NOP Import Certificates. Each shipment of
organic products imported into the United States must be declared as
organic to U.S. Customs and Border Protection (CBP) and associated with
a valid NOP Import Certificate (currently form NOP 2110-1).\61\ The NOP
Import Certificate contains specific information about the quantity and
source of a shipment of imported organic products. NOP Import
Certificates are currently used for organic products imported from
countries with which NOP has trade arrangements. This rulemaking will
expand and make compulsory the use of NOP Import Certificates,
regardless of an imported product's country of origin.
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\61\ Office of Management and Budget (OMB) approved form NOP
2110-1 NOP Import Certificate. https://www.ams.usda.gov/resources/nop-2110-1.
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In response to public comments, the final rule allows NOP Import
Certificates to be issued for a given time period (e.g., quarterly)
rather than with every shipment as proposed. AMS estimates that NOP
Import Certificates will be issued quarterly, as this will reduce costs
and limit disruption to the speed of imports. Additionally, the
estimated number of annual shipments has increased from 67,023 in 2017
to 80,109 in 2020 due to industry growth.\62\ Therefore, AMS estimates
3,856 exporters will request from their certifying agents an annual
total of 15,424 NOP Import Certificates,
[[Page 3612]]
covering 80,109 annual shipments.\63\ AMS estimates each exporter and
certifying agent will spend an average of 30 minutes to request and
approve each NOP Import Certificate. This estimate accounts for some
learning within the first year, as well as the option to issue a single
NOP Import Certificate for multiple shipments over a specific timeframe
and amount or volume. Additionally, AMS estimates that importers and
their certifying agents will need an average of one tenth (0.1) of an
hour, or 6 minutes, to compare the shipping manifest of each shipment
with its respective NOP Import Certificate to verify the accuracy and
organic compliance of each shipment.
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\62\ Data source: USDA Foreign Agricultural Service (FAS) Global
Agricultural Trade System (GATS). Select: Partners, World Total,
Product Type, Imports--General, Products: All Aggregates; Product
Groups: Organic--Selected: https://apps.fas.usda.gov/gats/default.aspx.
\63\ NOP International Division reports that 3,303 organic
exporters are certified by foreign (non-USDA) certifiers. Plus, the
Organic Integrity Database shows that 553 foreign-based handlers are
certified by USDA-accredited certifying agents. The total number of
NOP Import Certificates assumes each exporter is issued NOP Import
Certificates quarterly (four annually).
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Further, certifying agents must have and implement a documented
organic control system for intaking and approving or rejecting the
validity of an NOP Import Certificate request, and importers must have
and implement a documented organic control system to verify that
shipments of organic products are accompanied by accurate NOP Import
Certificate data and have not had contact with prohibited substances or
ionizing radiation (Sec. Sec. 205.273 and 205.300).
4. Clarifies nonretail containers used to ship or store organic
products must display organic identification and information that links
the container to audit trail documentation. This will help maintain the
integrity of organic products by reducing misidentification and
mishandling, facilitating traceability through the supply chain,
reducing organic fraud, and allowing accurate identification of organic
product by customs officials and transportation agents.
The rulemaking reduces burden because the revised regulation
requires less information on nonretail container labels and provides
exceptions for certain types of containers in response to public
comment. AMS estimates that 35,698 producers and/or processers will
need one tenth (0.1) of an hour, or 6 minutes, to add the required
information to the labels that are displayed on the nonretail
containers of an estimated 275,596 annual shipments (Sec.
205.307).\64\
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\64\ 29,929 (existing and new domestic operations and traders)
certified operations will be modifying how they label 195,387
nonretail shipments and 5,769 (existing, new, and domestic
operations and traders) certified operations will be modifying how
they label 80,109 nonretail shipments exported to the US.
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5. Codifies current practices for the certification of producer
group operations (groups of producers organized and certified as a
single operation).\65\ The rulemaking describes the criteria to qualify
as a producer group, how producer group operations must comply with the
USDA organic regulations, and how certifying agents should inspect
these operations. It also sets a risk-based benchmark to determine how
many producer group members in an operation need to be inspected by
certifying agents annually.
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\65\ NOP Policy Memo 11-10. Grower Group Certification, October
31, 2011: https://www.ams.usda.gov/sites/default/files/media/NOP-11-10-GroupGrowerCert.pdf.
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In response to public comment, AMS expects that these requirements
will add 11,800 hours of one-time paperwork burden for 5,900 producer
group operations \66\ to prepare a detailed Internal Control System for
their OSP, including procedures to address conflicts of interest and
manage the unique challenges of producer group oversight. In addition,
AMS estimates 5 hours to prepare and deliver training, outreach and
technical assistance to ICS personnel and producer group members,
leading to a total annual burden of 29,500 hours of burden annually
(Sec. Sec. 205.201, 205.400(g) and 205.403).
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\66\ Meinshausen F., Richter, T., Blockeel, J., and Huber, B.,
Group Certification: Internal Control Systems in Organic
Agriculture: Significance, Opportunities and Challenges, Research
Institute of Organic Agriculture FiBL, March 2019.
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6. Clarifies how certified operations may submit annual updates to
their OSP. This includes the option to only submit practices or
procedures that have changed since their last approved OSP, rather than
submitting an OSP in its entirety. This will reduce unnecessary
paperwork without compromising oversight because operations will
continue to maintain an OSP that accurately reflects current practices
and procedures of the operation. This codifies current policy and does
not modify the paperwork burden (Sec. 205.406).
7. Requires certifying agents to issue standardized certificates of
organic operation generated from the USDA's publicly available Organic
Integrity Database (OID).\67\ This will require an initial upload of
mandatory data for each operation and maintenance to ensure that data
in OID are current and accurate. Currently, all certifying agents have
voluntarily uploaded data and maintain an estimated 50% or more data on
all certified operations per the recommendations found in the NOP's
Data Quality Best Practices.\68\
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\67\ Organic Integrity Database: https://organic.ams.usda.gov/integrity. Accessed September 2021.
\68\ Data Quality Best Practices: https://www.ams.usda.gov/sites/default/files/media/INTEGRITY%20Data%20Quality.pdf.
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These amendments will require a new, one-time burden of reporting
hours for certifying agents to upload existing data pertaining to
currently certified operations into OID for the first time. It is
estimated that uploading these data into OID will require 30 minutes
for each operation and will be performed by administrative support
personnel who have a lower wage rate than review and compliance staff.
The rulemaking's burden increases slightly due to industry growth.
These amendments will simultaneously eliminate the requirement to
physically mail the Administrator or State organic program paper copies
of: (1) the list of operations certified annually; (2) notifications of
proposed adverse actions, approvals, or denials of corrective actions;
and (3) notifications of executions of adverse actions regarding
certified operations or operations applying for certification
(Sec. Sec. 205.405 and 205.501). AMS is not modifying the estimate of
paperwork burden associated with these changes in requirements because
any change will be very small, and these activities and tasks are still
occurring electronically as a part of maintaining the data on all
operations over time.
8. Requires certifying agents to develop procedures to: (1)
identify high-risk operations and agricultural products; (2) conduct
supply chain traceability audits, (3) share information with other
certifying agents to verify supply chains and conduct investigations,
and (4) report credible evidence of organic fraud to the USDA. Due to
the complexity of these procedures, AMS estimates each certifying agent
will spend two hours documenting these procedures (Sec. Sec. 205.501
and 205.504) rather than one hour as proposed. The rulemaking's burden
increases due to an increase in time for preparing procedures despite a
net loss of certifying agents since 2017 (the net value reflects that
while some certifiers have been suspended or have surrendered, others
have been newly accredited).
9. Requires certifying agents to submit their decision criteria for
acceptance of mediation, and a process for identifying personnel to
conduct mediation and set up mediation sessions with its administrative
policies and procedures required by Sec. 205.504(b). AMS estimates
each certifying agent will spend one
[[Page 3613]]
hour documenting these procedures, which they are already implementing.
The rulemaking's burden changes due to the net loss of 3 certifying
agents since 2017.
10. Requires certifying agents to establish procedures to conduct
inspector field evaluations (``witness inspections''), demonstrate that
they are sufficiently staffed with qualified personnel, and demonstrate
that all inspectors, certification reviewers, and in-field evaluators
meet knowledge, skills, and experience qualifications. AMS estimates
that each certifying agent will spend 60 minutes to draft policies and
procedures for conducting inspector field evaluations. Further,
certifying agents must observe an inspector performing an on-site
inspection at least once every three years (or annually for inspectors
with fewer than three years of experience).
The rulemaking's burden is reduced due to narrowed training
requirements and the net loss of 3 certifying agents since 2017. AMS
estimates each certifying agent will conduct an average of two field
evaluations of an inspector and certification review personnel per
year, rather than four as proposed, and that this activity will require
7.5 hours per evaluation (Sec. Sec. 205.2 and 205.501).
11. Requires some additional training of new inspectors and
certification review personnel. Inspectors and certification review
personnel play a crucial role in determining whether an operation is
granted organic certification initially and whether certified
operations comply with the USDA organic regulations. Certification
review personnel may also serve as inspectors. Through insight gained
during regular audits of certifying agents, AMS estimates that
inspectors and certification review staff currently receive at least 10
hours of training per year from certifying agents on topics related to
the USDA organic regulations.
In response to public comment, 40 hours of additional training is
required for inspectors and certification review personnel with less
than one year of experience.\69\ Based on an estimated separation rate
of 14 percent,\70\ AMS estimates that certifying agents will annually
hire 35 new certification review staff and hire or contract with 35
inspectors with less than one year of experience to replace the
certification review staff and inspectors that exit the labor pool.
Training offered by NOP through its online Organic Integrity Learning
Center (OILC) and training provided by the certifying agents or other
providers may qualify towards the minimum annual training requirements
(Sec. Sec. 205.2 and 205.501).
---------------------------------------------------------------------------
\69\ Ten hours of training are accounted for in the 2020
Information Collections Renewal for NOP (AMS-NOP-19-0090; OMB
Control Number: 0581-0191). Our internal on-site accreditation audit
checklist used by our accreditation audit team includes a question
on training. With the implementation of this rule, the specific
hours of training offered by the 75 certifying agents will be
documented.
\70\ The US Bureau of Labor and Statistics reports that the
average separation rate (which captures both labor force exits and
transfers in occupation) for agricultural inspectors is 14 percent.
https://www.bls.gov/news.release/jolts.t16.htm.
---------------------------------------------------------------------------
12. Requires that certifying agents conduct unannounced inspections
of at least 5 percent of the operations they certify, which is the
current recommended practice in NOP Instruction 2609.\71\ For the
purposes of estimating paperwork impacts, AMS expects that half of the
unannounced inspections (2.5% of total inspections) will meet the
requirement for a full annual inspection and will not impact current
paperwork burden. The remaining half of the unannounced inspections
(2.5% of total inspections) will be limited in scope and target high-
risk operations and will not count as a full annual inspection.
Examples of targeted, limited-scope unannounced inspections include but
are not limited to verifying livestock on pasture or performing
targeted mass-balance or traceability audits. AMS estimates that the
paperwork impacts associated with these unannounced inspections will
average inspectors 5 hours per inspection; half of the estimated 10
hours for a full annual inspection (Sec. 205.403).
---------------------------------------------------------------------------
\71\ NOP 2609, Instruction, Unannounced Inspections. September
12, 2012. Available in the NOP Program Handbook: https://www.ams.usda.gov/sites/default/files/media/2609.pdf.
---------------------------------------------------------------------------
13. Clarifies the process for accepting foreign conformity
assessment systems that oversee organic certification in foreign
countries.\72\ The OFPA (7 U.S.C. 6505(b)) and the USDA organic
regulations provide the authority to establish organic equivalency. The
revised regulations describe the criteria, scope, and other parameters
for ongoing peer review audits of foreign organic conformity systems to
determine whether the United States should continue, revise, or
terminate such equivalence determinations. These peer review audits of
equivalence determinations occur as needed and will result in new
periodic paperwork impacts for foreign governments. The rulemaking's
burden is reduced because AMS estimates it will review one foreign
government conformity assessment system per year. AMS estimates the
reporting impacts for foreign governments when USDA reviews the
applicable trade arrangement or agreement to be 60 hours. Since
recordkeeping is ongoing requirement, recordkeeping is calculated as 10
hours per year per foreign government. These impacts are comparable to
the estimated paperwork impacts for AMS audits of certifying agents
(Sec. 205.511).
---------------------------------------------------------------------------
\72\ Currently, the United States has established organic trade
arrangements with Canada, the European Union, the United Kingdom,
Israel, Japan, New Zealand, South Korea, Taiwan, and Switzerland.
---------------------------------------------------------------------------
Respondents
AMS has identified four primary types of entities (respondents)
that will need to submit and maintain information as a result of this
rulemaking: certified organic operations; accredited certifying agents;
organic inspectors; and foreign governments. Three respondent types--
certified operations (producers and handlers), certifying agents, and
inspectors--have been identified in a currently approved information
collection (0581-0191). To implement a 2018 Farm Bill mandate, AMS is
requiring certification of additional types of operations in the
organic supply chain and regular audits of trade arrangements or
agreements with foreign governments.\73\ This adds new types of
handlers as a subcategory of certified operations and foreign
governments as a new type of respondent.
---------------------------------------------------------------------------
\73\ See Section 10104(a) of the Agriculture Improvement Act of
2018, Public Law No: 115-334, available at: https://www.congress.gov/115/plaws/publ334/PLAW-115publ334.pdf.
---------------------------------------------------------------------------
To more precisely understand the paperwork impacts of this
rulemaking, AMS has divided the categories of respondents into domestic
and foreign, as appropriate, to show the potential impacts on domestic-
based versus foreign-based USDA-accredited certifying agents,
inspectors, and certified operations, along with foreign-accredited
certifying agents, and foreign governments serving as accrediting
bodies. For each type of respondent, we describe the general paperwork
submission and recordkeeping activities and estimate: (1) the number of
respondents; (2) the hours they spend, annually, creating and storing
records to meet the paperwork requirements of the organic labeling
program; and (3) the costs of those activities based on prevailing
domestic and foreign wages and benefits.
Certifying Agents
Certifying agents are State, private, or foreign entities
accredited by the USDA,
[[Page 3614]]
or by accreditation bodies of foreign governments with which USDA has a
trade arrangement or agreement. Certifying agents certify domestic and
foreign producers and handlers as organic in accordance with the OFPA
and the USDA organic regulations. Certifying agents determine whether a
producer or handler meets the organic requirements, using detailed
information from the operation about its specific practices and on-site
inspection reports from organic inspectors.
Currently, there are 75 USDA-accredited certifying agents (down
from 78 in 2017) 45 are based in the United States and 30 are
headquartered in foreign countries. Both domestic- and foreign-based
USDA-accredited certifying agents certify operations based in the
United States and abroad. AMS assumes all currently accredited
certifying agents evaluate all types of production and handling
operations for compliance with the USDA organic regulations and will be
subject to the reporting and recordkeeping burdens of this rulemaking.
In addition, AMS assumes there are 30 foreign government-accredited
foreign-based certifying agents that certify handlers in accordance
with the USDA organic regulations and that will issue NOP Import
Certificates for organic product shipments to the United States.\74\
---------------------------------------------------------------------------
\74\ An estimate based on the number of foreign-based USDA-
accredited certifying agents.
---------------------------------------------------------------------------
Certifying agents of operations that export to the United States
must issue NOP Import Certificates for all shipments of organic
products being exported. The USDA Foreign Agricultural Service (FAS)
Global Agricultural Trade System (GATS) showed 80,109 shipments of
organic product coming into the United States in 2020 (up from 67,023
in 2017 due to industry growth).\75\ In response to public comments,
AMS estimates that NOP Import certificates will be issued seasonally
(e.g., quarterly) rather than with every shipment as proposed. AMS
estimates that 3,856 foreign exporters will request from their
certifying agents an annual total of 15,424 NOP Import Certificates,
covering 80,109 annual shipments.\76\ AMS estimates each exporter and
certifying agent will spend 30 minutes to request and approve each NOP
Import Certificate.
---------------------------------------------------------------------------
\75\ Data source: USDA Foreign Agricultural Service (FAS) Global
Agricultural Trade System (GATS). Select: Partners, World Total,
Product Type, Imports--General, Products: All Aggregates; Product
Groups: Organic--Selected: https://apps.fas.usda.gov/gats/default.aspx.
\76\ NOP International Division reports that 3,303 organic
exporters are certified by foreign (non-USDA) certifiers. Plus, the
Organic Integrity Database shows that 553 foreign-based handlers are
certified by USDA-accredited certifying agents. The total number of
NOP Import Certificates assumes each exporter is issued NOP Import
Certificates quarterly (four annually).
---------------------------------------------------------------------------
Thirty (30) USDA-accredited certifying agents based in foreign
countries certify 92% of the foreign operations certified under USDA
organic standards. Of the 45 domestic-based USDA accredited certifying
agents, 15 certifying agents certify 8% of the foreign operations
certified under USDA.\77\ This means that 30 domestic-based USDA-
accredited certify agents only certify domestic-based operations that
do not import foreign organic products or ingredients. AMS estimates
there are 30 foreign-accredited certifying agents that certify foreign
operations under trade arrangements.\78\
---------------------------------------------------------------------------
\77\ Organic Integrity Database: https://organic.ams.usda.gov/integrity/.
\78\ An estimate based on the number of foreign-based USDA-
accredited certifying agents.
---------------------------------------------------------------------------
AMS will review documents regarding imports during the
accreditation audits of USDA-accredited certifying agents. AMS
estimates 30 minutes for the 3,856 exporters and their certifying
agents to prepare and approve each of the 15,424 NOP Import
Certificates and one tenth of an hour, or 6 minutes, for importers to
verify and reconcile all 80,109 subsequent associated shipments
exported to the United States.\76\ USDA-accredited domestic-based
certifying agents must work with their foreign-based operations to
verify their associated shipments for 8%, or 6,409, of 80,109 annual
shipments. USDA-accredited foreign-based certifying agents must work
with their foreign-based operations to verify their associated
shipments for 46%, or 36,850, of 80,109 annual shipments. Foreign-
accredited certifying agents must work with their foreign-based
operations to verify 46% of 80,109 annual shipments.
In addition, this rulemaking reduces the current paperwork burden
of accredited certifying agents by eliminating the need to provide
notices of approval or denial of certification to the Administrator
following the issuance of a notice of noncompliance or adverse action
to an applicant for certification. Also, the rulemaking removes the
annual requirement for certifying agents to submit by January 2 an
annual list of operations certified. Certifying agents will instead be
required to update data in OID for each operation they certify. AMS is
not modifying the estimate of paperwork burden with these changes in
requirements because any change will be very small. These activities
and tasks are still occurring electronically as a part of maintaining
the data on all operations over time. Certifying agents must issue
organic certificates generated in OID.
[[Page 3615]]
In addition, all USDA-accredited certifying agents must write
detailed procedures to identify high-risk operations and products they
certify and procedures to conduct supply-chain traceability audits.
Certifying agents must write fraud prevention and reporting procedures,
and mediation procedures per Sec. 205.504(b). Certifying agents must
write procedures to demonstrate how they are sufficiently staffed and
that all persons who perform certification review activities and on-
site inspections (inspectors) are qualified and complying with training
requirements for their new certification review personnel. AMS
estimates that 14 percent, or 35, new certification review staff with
less than one year of experience must complete 40 hours of training in
their first year in addition to the baseline training requirement of 10
hours annually already accounted for in the overall program ICR
(0191).79 80
---------------------------------------------------------------------------
\79\ Ten hours of training are accounted for in the 2020
Information Collections Renewal for the NOP (AMS-NOP-19-0090; OMB
Control Number: 0581-0191). Our internal onsite accreditation audit
checklist used by our accreditation audit team includes a question
on training. With the implementation of this rule, the specific
hours of training offered by our 75 certifying agents will be
documented.
\80\ The US Bureau of Labor and Statistics reports that the
average separation rate (which captures both labor force exits and
transfers in occupation) for agricultural inspectors is 14 percent.
https://www.bls.gov/news.release/jolts.t16.htm.
---------------------------------------------------------------------------
This rulemaking increases the overall reporting and recordkeeping
burden for certifying agents (See Summary Table 1: Certifying Agents).
AMS estimates the annual collection cost per domestic-based USDA-
accredited certifying agents will be $13,511.\81\ This cost is based on
an estimated 109.23 labor hours per certifying agent per year for staff
with certification review responsibilities at $47.97 per labor hour,
including 31.7% benefits, for a total salary component of $5,229 per
year.\82\ The estimated cost for domestic certifying agents also
includes 332.55 labor hours per certifying agent per year for
administrative support staff to upload data about certified operations
to OID at $24.90 per labor hour, including 31.7% benefits, for a total
salary component of $8,282 per year.\83\
---------------------------------------------------------------------------
\81\ In this assessment, all domestic labor rates are sourced
from the U.S. Bureau of Labor Statistics National Compensation
Survey, Occupational Employment and Wages, May 2020: https://www.bls.gov/oes/current/oes_nat.htm. Domestic benefits are based on
a Bureau of Labor Statistics News Release on Employer Costs for
Employee Compensation, which states that benefits account for 31.7%
of total average employer compensation costs, December 17, 2020.
\82\ The labor rate for certification review staff is based on
Occupational Employment Statistics group 13-1041, Compliance
Officers. Compliance officers examine, evaluate, and investigate
eligibility for or conformity with laws and regulations governing
contract compliance of licenses and permits, and perform other
compliance and enforcement inspection and analysis activities not
classified elsewhere. Compliance Officers (bls.gov).
\83\ The labor rate for administrative support staff is based on
Occupational Employment Statistics group 43-9199, Office and
Administrative Support Workers, who support general office work and
data entry functions. Office and Administrative Support Workers, All
Other (bls.gov).
---------------------------------------------------------------------------
In addition, AMS estimates the annual collection cost for all
domestic-based USDA-accredited certifying agents will be $608,001. This
cost is based on a total of 4,915 hours for all staff with
certification review responsibilities at $47.87 per labor hour,
including 31.7% benefits, for a total salary component of $235,313 for
all staff with certification review and procedure writing
responsibilities of all domestic-based USDA-accredited certifying
agents. The estimated cost for all domestic-based certifying agents
also includes 14,965 hours total hours for administrative support staff
uploading data about certified operations to OID at $24.90 per labor
hour, including 31.7% benefits for a total salary component of
$372,688.
Summary Table 1--Certifying Agents
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cost per
Respondent categories Number of Wages + Hours per respondent Total all Total all costs
respondents benefits respondent type hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
US Based USDA Certifying Agents.............................. 45 $47.87 109.23 $5,229.17 4,915.36 $235,312.78
US Based USDA Certifying Agents--data entry.................. 45 24.90 332.55 8,281.95 14,964.69 372,687.76
------------------------------------------------------------------------------------------
Subtotal U.S.-Based USDA Certifying Agents............... 45 ........... 441.78 13,511.12 19,880.05 608,000.54
------------------------------------------------------------------------------------------
Foreign-Based USDA Certifying Agents......................... 30 34.40 653.80 22,493.03 19,614.07 674,791.04
Foreign-Based USDA Certifying Agents--data entry............. 30 17.90 346.64 6,203.93 10,399.19 186,118.00
------------------------------------------------------------------------------------------
Subtotal Foreign-Based USDA Certifying Agents............ 30 ........... 1,000.44 28,696.97 30,013.26 860,909.04
------------------------------------------------------------------------------------------
Total USDA Accredited Certifying Agents...................... 75 ........... .............. 42,208.09 49,893.31 1,468,909.58
------------------------------------------------------------------------------------------
Foreign (Non-USDA) Accredited Certifying Agents.............. 30 34.40 614.17 21,129.51 18,425.07 633,885.38
All Certifying Agents........................................ 105 ........... .............. .............. 68,318.38 2,102,794.96
--------------------------------------------------------------------------------------------------------------------------------------------------------
For foreign-based USDA-accredited certifying agents, AMS estimates
the annual cost per certifying agent will be $28,697 per year. This
cost is based on an estimated 653.80 labor hours for staff with
certification review and procedure writing responsibilities at $34.40
per labor hour, including 34.63% benefits, for a total salary component
of $22,493 per foreign-based USDA-accredited certifying agent per year.
These estimated costs primarily pertain to the issuance and review of
NOP Import Certificates. The estimated cost for foreign-based USDA-
accredited certifying agents also includes 346.64 labor hours per
certifying agent per year for administrative support staff to upload
data about certified operations to OID at $17.90 per labor hour,
including 34.63% benefits, for a total salary component of $6,204 per
year.84 85
---------------------------------------------------------------------------
\84\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents, which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\85\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
AMS estimates the annual collection cost for all foreign-based USDA
accredited certifying agents will total $860,909. This cost is based on
a total of 19,614.07 hours for all staff with certification review
responsibilities at $24.90 per labor hour, including 34.63% benefits,
for a total salary component of $674,791 for staff with certification
review and procedure writing responsibilities of all foreign-based
USDA-accredited certifying agents. The estimated cost for all foreign-
based USDA-accredited certifying agents also includes 10,399.19 hours
total hours for administrative support staff uploading data about
certified operations to OID at $17.90 per labor hour, including 34.63%
[[Page 3616]]
benefits, for a total salary component of $186,118.86 87
---------------------------------------------------------------------------
\86\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\87\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
For foreign-accredited certifying agents (non-USDA accredited), AMS
estimates the annual cost will be $21,130 per certifying agent. This
cost is based on an estimated 614.17 labor hours per year for staff to
issue and review NOP Import Certificates, at $34.40 per labor hour plus
34.63% benefits. The total for all foreign-accredited certifying agents
is estimated to be $633,885. The cost is based on an estimated 18,425
total hours for all staff involved in the issuance and review of NOP
Import Certificates, at $34.40 per labor hour plus 34.63% benefits.
88 89
---------------------------------------------------------------------------
\88\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD.agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\89\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
The total cost for all certifying agents--including the 75 USDA-
accredited certifying agents, domestic- and foreign-based, and the
estimated 30 foreign-accredited (non-USDA) certifying agents who
certify operations that export products to the U.S.--is $2,102,795.
This cost is based on 68,318.38 total hours at their respective wage
rates and benefits to comply with the rulemaking's requirements.
Organic Inspectors
Inspectors conduct on-site inspections of certified operations and
operations applying for certification and report the findings to the
certifying agent. Inspectors may be independent contractors or
employees of certifying agents. Certified operations must be inspected
annually, and a certifying agent may call for additional inspections or
unannounced inspections on an as-needed basis (Sec. 205.403(a)). Any
individuals who apply to conduct inspections of operations will need to
submit information documenting their qualifications to the certifying
agent (Sec. 205.504(a)(3)).
Inspectors provide an inspection report to the certifying agent for
each operation inspected (Sec. 205.403(e)) but are not expected to
store the record. Currently, AMS estimates that inspectors spend 10
hours on average to complete an inspection report for a full annual
inspection of an organic operation. The additional unannounced
inspections required by this rulemaking are likely to be more limited
in scope (such as pasture or dairy surveillance, or mass-balance and
supply chain traceability audits). AMS projects, on average, that
inspectors will spend 5 hours to complete an inspection report for an
unannounced targeted-scope inspection. Organic inspectors do not have
recordkeeping obligations; certifying agents maintain the records of
inspection reports (see Summary Table 2: Inspectors).
Summary Table 2--Inspectors
--------------------------------------------------------------------------------------------------------------------------------------------------------
Cost per
Respondent categories Number of Wages + Hours per respondent Total all Total all costs
respondents benefits respondent type hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
USDA US based Inspectors..................................... 148 $30.79 30.86 $950.20 4,567.17 $140,629.94
USDA Foreign based inspectors................................ 102 22.13 31.12 688.53 3,173.80 70,229.73
------------------------------------------------------------------------------------------
All USDA Inspectors...................................... 250 ........... .............. .............. 7,740.97 210,859.67
--------------------------------------------------------------------------------------------------------------------------------------------------------
According to the International Organic Inspectors Association
(IOIA), there are approximately 250 inspectors currently inspecting
crop, livestock, handling, and/or wild crop operations that are
certified or have applied for certification. To comply with this
rulemaking, AMS estimates that 14 percent, or 35, new inspectors with
less than one year of experience must complete 40 hours of training in
their first year in addition to the baseline training requirement of 10
hours annually already accounted for in the overall program ICR
(0191).90 91
---------------------------------------------------------------------------
\90\ Ten hours of training are accounted for in the 2020
Information Collections Renewal for the NOP (AMS-NOP-19-0090; OMB
Control Number: 0581-0191). Our internal onsite accreditation audit
checklist used by our accreditation audit team includes a question
on training. With the implementation of this rule, the specific
hours of training offered by our 75 certifying agents will be
documented.
\91\ The US Bureau of Labor and Statistics reports that the
average separation rate (which captures both labor force exits and
transfers in occupation) for agricultural inspectors is 14 percent.
https://www.bls.gov/news.release/jolts.t16.htm.
---------------------------------------------------------------------------
AMS estimates that 148 inspectors are working for USDA-accredited
certifying agents in the United States. For the additional training of
new inspectors, and for conducting unannounced targeted-scope
inspections, AMS estimates the annual paperwork impact cost per
domestic-based inspector is $950.20. This is based on an estimated
30.86 labor hours per year at $30.79 per labor hour, including 31.7%
benefits. The total annual cost for all domestic-based inspectors is
$140,630. This cost is based on 4,567 total hours for all domestic
based inspectors at $30.79 per labor hour, including 31.7%
benefits.\92\
---------------------------------------------------------------------------
\92\ The labor rate for inspectors is based on Occupational
Employment Statistics group 45-2011, Agricultural Inspectors.
Agricultural inspectors inspect agricultural commodities, processing
equipment, facilities, and fish and logging operations to ensure
compliance with regulations and laws governing health, quality, and
safety.
---------------------------------------------------------------------------
AMS estimates that 102 inspectors are working for USDA-accredited
certifying agents in foreign countries. AMS estimates the annual
paperwork impact cost per foreign-based inspector is $688.53. This
estimate is based on an estimated 31.12 labor hours per year at $22.13
per labor hour, including 34.63% benefits for the additional training
of new inspectors and for conducting unannounced targeted-scope
inspections. This rule does not impose additional recordkeeping costs
for inspectors. The total annual cost for all foreign-based inspectors
is $70,230 at $31.12 per labor hour, including 34.63% benefits. The
total annual cost for all inspectors working for USDA-accredited
certifying agents is $210,860, at their respective wage rates and
benefits.93 94
---------------------------------------------------------------------------
\93\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\94\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
[[Page 3617]]
Producers and Handlers
Domestic and foreign producers and handlers seeking organic
certification must submit an OSP that details the practices and
activities specific to their operation. Once certified, operations are
required to update any changes in their operation or practices to their
certifying agent at least annually.
Uncertified Handlers. This rulemaking requires that operations that
facilitate the sale or trade of organic products--including, but not
limited to, certain brokers, importers, and traders--obtain organic
certification and submit and maintain an OSP. AMS estimates that 1,985
domestic \95\ and 1,379 foreign-based \96\ operations will need to
become certified as a result of the rule. Traders and brokers do not
farm or manufacture organic products, so the OSPs for traders and
brokers will address fewer sections of USDA organic regulations than
OSPs for operations that produce or manufacture organic products.
Certifying agents customize the format of the OSP to cover standards
applicable to the operations seeking certification. Therefore, AMS
estimates that preparation of an initial OSP will require 40 reporting
hours, plus 10 hours of annual recordkeeping. The estimated annual
reporting burden for each entity to update its OSP in future years is
20 hours (See Summary Table 3a: Uncertified Handlers).
---------------------------------------------------------------------------
\95\ Please refer to the ``Applicability and Exemptions from
Certification (Sec. Sec. 205.100-101)'' chapter in the Regulatory
Impact Analysis (RIA) for an explanation of how previously excluded
domestic handlers were estimated.
\96\ AMS assumes the 1,985 domestic excluded operations
represent 59% of the global total benchmarked 59%/41% ratio of
domestic to foreign operations and certifying agents. Therefore, AMS
estimate there are an additional 1,379 foreign formerly excluded
operations, for a total of 3,364 new handlers that will need organic
certification.
---------------------------------------------------------------------------
All operations that export organic products to the United States
must request an NOP Import Certificate from their certifying agent.
Further, operations that import organic products must verify and
reconcile each shipment with its associated NOP Import Certificate and
verify that organic integrity was maintained throughout the import
process. In addition, domestic and foreign handlers that must obtain
organic certification as a result of this rulemaking will also need to
comply with the labeling requirements for nonretail containers.
Summary Table 3a--Uncertified Handlers
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total cost per
Respondent categories Number of Wages + Total hours respondent Total all Total all costs
respondents benefits per respondent type hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Formerly Excluded Handlers--Domestic......................... 1,985 $48.64 50.97 $2,478.80 101,166.47 $4,920,414.48
Formerly Excluded Handlers--Foreign.......................... 1,379 34.95 53.42 1,867.02 73,660.94 2,574,623.40
------------------------------------------------------------------------------------------
All Uncertified Handlers................................. 3,364 ........... .............. .............. 174,827.41 7,495,037.88
--------------------------------------------------------------------------------------------------------------------------------------------------------
AMS estimates the annual paperwork impact for each domestic handler
to prepare their initial organic system plan, verify and reconcile
imported shipments with their respective NOP Import Certificates, and
verify that the organic integrity of the product was maintained through
shipping is 2,478.80. This is based on an estimated 50.97 labor hours
at $48.64 per labor hour, including 31.7% benefits. The total cost to
all previously uncertified domestic handlers is $4,920,415. This cost
is based on 101,166.47 total labor hours at $48.64 per labor hour,
including 31.7% benefits.\97\
---------------------------------------------------------------------------
\97\ For uncertified handlers, AMS chose to use the same labor
rate as certified producers and handlers: Occupational Employment
Statistics group 11-9013, Farmers, Ranchers, and Other Agricultural
Managers.
---------------------------------------------------------------------------
AMS estimates the annual paperwork impact for each foreign-based
handler to prepare their initial organic system plan and to work with
their certifying agent to prepare NOP Import Certificates for the
products they export is $1,867.02. This is based on an estimated 53.42
labor hours per year at $34.95 per labor hour, which includes 34.63%
for benefits. The total cost to all previously uncertified foreign
handlers is $2,574,623.40. This cost is based on 73,660.94 total labor
hours at $34.95 per labor hour, which includes 34.63% for benefits.
Total costs to the 3,364 previously uncertified handlers, domestic and
foreign, is $7,495,038, based on 174,827 total labor hours at their
respective domestic and foreign wage rates and benefits. This cost is
to prepare and keep initial OSPs and related records, and to prepare,
verify, and reconcile NOP Import Certificates for
compliance.98 99
---------------------------------------------------------------------------
\98\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD.agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\99\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
Certified Operations and New Applicants under Current Rules. There
currently are 44,725 organic operations worldwide that are certified to
the USDA organic standards. Over the next 12 months, AMS expects 2,639
operations will seek organic certification, based on the 5.9% rate of
growth in number of operations observed in the last 12 months under
current rules. Therefore, AMS estimates that 27,945 operations based in
the United States, and 19,419 operations based in foreign countries,
including the respective applicants for certification, will be impacted
by this rulemaking.\100\
---------------------------------------------------------------------------
\100\ Organic Integrity Database: https://organic.ams.usda.gov/integrity/.
---------------------------------------------------------------------------
All currently certified organic operations and projected new
applicants must describe in their OSP their procedures for monitoring,
verifying, and demonstrating the organic status of their suppliers and
products received to prevent organic fraud. All certified organic
operations must also comply with revised nonretail container labeling
requirements and must maintain all records about their organic
production and/or handling for five years (Sec. 205.103(b)(3)).
[[Page 3618]]
In addition, AMS estimates a one-time paperwork burden of 11,800
hours for 5,900 producer group operations to prepare a detailed
Internal Control System (ICS) for their OSP, including procedures to
address conflicts of interest and manage the unique challenges of
producer group oversight. In addition, training requirements for ICS
personnel and producer group members are expanded to 29,500 hours
annually (Sec. Sec. 205.201, 205.400(g) and 205.403).\101\
---------------------------------------------------------------------------
\101\ Meinshausen F., Richter, T., Blockeel, J., and Huber, B.,
Group Certification: Internal Control Systems in Organic
Agriculture: Significance, Opportunities and Challenges, Research
Institute of Organic Agriculture FiBL, March 2019.
Summary Table 3b--Certified Organic Operations and New Applicants
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total cost/
Respondent categories Number of Wages + Total hours/ respondent Total all Total all costs
respondents benefits respondent type hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Certified Producers & Handlers--New and Existing Domestic.... 27,945 $48.64 1.67 $81.07 46,579.60 $2,265,483.08
Certified Producers & Handlers--New and Existing Foreign..... 19,419 34.95 3.44 120.39 66,888.32 2,337,904.67
------------------------------------------------------------------------------------------
All New and Existing Producers & Handlers.................... 47,364 ........... .............. .............. 113,467.92 4,603,388.08
--------------------------------------------------------------------------------------------------------------------------------------------------------
AMS estimates that the average annual paperwork impact for domestic
USDA-certified organic producers and handlers to develop fraud
prevention procedures and to comply with nonretail container labeling
requirements is $81.07. This is based on an estimated 1.67 labor hours
at $48.64 per labor hour, including 31.7% benefits. The total cost for
all domestic certified organic producers and handlers to comply with
these new requirements is $2,265,483.08. This cost is based on
46,579.60 labor hours at $48.64 per labor hour, including 31.7%
benefits.\102\
---------------------------------------------------------------------------
\102\ The labor rate for producers and handlers is based on
Occupational Employment Statistics group 11-9013, Farmers, Ranchers,
and Other Agricultural Managers, who plan, direct, or coordinate the
management or operation of farms, ranches, or other agricultural
establishments.
---------------------------------------------------------------------------
AMS estimates the average annual paperwork impact for foreign-based
USDA-certified organic producers and handers to create fraud prevention
procedures and to comply with nonretail container labeling requirements
is $120.39. This is based on an estimated 3.44 labor hours per year at
$34.95 per labor hour, including 34.63% benefits. The total cost for
all foreign producers and handlers certified to the USDA organic
standards is $2,337,904.67. This cost is based on 66,888.32 labor hours
year at $34.95 per labor hour, including 34.63% benefits. The total
cost for the 47,364 current and projected certified organic producers
and handlers, domestic and foreign, is $4,603,388. This cost is based
on 113,4677.92 labor hours at their respective domestic and foreign
wages and benefits.103 104
---------------------------------------------------------------------------
\103\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\104\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
Foreign Governments
The U.S. government, including the USDA and the U.S. Trade
Representative, work closely together to implement processes that
determine the equivalence of foreign organic certification programs and
then negotiate an arrangement or agreement as appropriate.\105\
Formerly, the organic regulations only addressed this authority in
general terms under Sec. 205.500(c) but did not describe the criteria,
scope, and other parameters to establish, oversee, or terminate such
arrangements or agreements. The rulemaking describes equivalence
determinations in more detail; this creates a new type of PRA
respondent category. The rulemaking allows an equivalence determination
if the U.S. government determines that the technical requirements and
conformity assessment system under which foreign products labeled as
organic are produced and handled are at least equivalent to the
requirements of the OFPA and the USDA organic regulations. The
rulemaking requires periodic assessment.
---------------------------------------------------------------------------
\105\ The United States currently has organic trade arrangements
with Canada, the European Union, the United Kingdom, Israel, Japan,
New Zealand, South Korea, Taiwan, and Switzerland.
---------------------------------------------------------------------------
AMS expects these periodic peer review assessments will be similar
in depth and frequency to the audits of USDA-accredited certifying
agents and estimates a comparable level of reporting and recordkeeping
burden by foreign governments with which USDA has negotiated trade
arrangements or agreements. AMS estimates the collection cost for the
periodic review of a single foreign government is $602. This cost is
based on 7.5 reporting labor hours averaged as needed and an estimated
10 hours of annual recordkeeping per foreign government per year at
$24.59 per labor hour, including 34.63% benefits, for a total salary
component of $602.06 per year reviewed. The total cost for foreign
governments to be assessed for a trade arrangement or agreement is
$4,816. This cost is averaged as 140 total labor hours for all foreign
governments at $24.59 per labor hour, including 34.63% benefits.
106 107
---------------------------------------------------------------------------
\106\ The source of the data is based on average World Bank wage
rates for countries with USDA-accredited certifying agents which
were 70.3% of U.S. labor rates in 2020. https://data.worldbank.org/indicator/NY.GDP.PCAP.PP.CD. Agents: https://stats.oecd.org/Index.aspx?DataSetCode=AWCOMP.
\107\ Benefits are based on a review of data from the
Organisation for Economic Co-Operation and Development (OECD), which
indicates that benefits account for 34.63% of total compensation in
foreign countries with USDA-accredited certifying agents.
---------------------------------------------------------------------------
Total (Domestic and Foreign) Information Collection Cost (Reporting
and Recordkeeping) of Rulemaking: $14,416,897 (Also, see Summary Table
4: All Reporting and Recordkeeping Hours and Costs, and All Domestic
Reporting and Recordkeeping Hours and Costs).
Total All Reporting Burden Cost: $12,454,097.
Estimate of Burden: Public reporting burden for the collection of
information is estimated to average 0.56 hours per year per response.
Respondents: Certifying agents, certified operations, inspectors,
and foreign governments.
Estimated Number of Reporting Respondents: 51,091.
Estimated Number of Reporting Responses: 566,387.
Estimated Total Annual Burden on Reporting Respondents: 318,859
hours.
Estimated Total Annual Reporting Responses per Reporting
Respondents: 11.09 reporting responses per reporting respondents.
Total All Recordkeeping Burden Cost: $1,962,800.
Estimate of Burden: Public recordkeeping burden is estimated to be
[[Page 3619]]
an annual total of 0.90 hours per year per respondent.
Respondents: Certifying agents, certified operations, and foreign
governments.
Estimated Number of Recordkeeping Respondents: 50,811.
Estimated Total Recordkeeping Burden on Respondents: 45,636 hours.
Estimated Total Recordkeeping Responses per Recordkeeping
Respondents: 1 recordkeeping response per recordkeeping respondents.
Total Domestic Only Information Collection Cost (Reporting and
Recordkeeping) of Rulemaking: $7,934,528.
Total Domestic Only Reporting Burden Cost: $6,627,301.
Estimate of Burden: Public domestic only reporting burden is
estimated to be an annual total 0.43 hours per year per domestic
respondent.
Respondents: Certifying agents, certified operations, and
inspectors.
Estimated Number of Domestic Reporting Respondents: 30,123.
Estimated Number of Domestic Reporting Responses: 334,168.
Estimated Total Annual Reporting Burden on Domestic Respondents:
145,315 hours.
Estimated Total Domestic Reporting Responses per Reporting
Respondents: 11.09 reporting response per reporting respondents.
Total Domestic Only Recordkeeping Burden Cost: $1,307,227.
Estimate of Burden: Public domestic only recordkeeping burden is
estimated to be an annual total of 1 hours per year per respondent.
Respondents: Certifying agents and certified operations.
Estimated Number of Domestic Recordkeeping Respondents: 29,975.
Estimated Total Annual Recordkeeping Burden on Domestic
Respondents: 26,878 hours.
Estimated Number of Domestic Recordkeeping Responses: 29,929.
Estimated Total Domestic Recordkeeping Responses per Recordkeeping
Respondents: 1 recordkeeping response per recordkeeping respondents.
Summary Table 4--All Hours and Costs, All Domestic Hours and Costs, and All Foreign Hours and Costs
----------------------------------------------------------------------------------------------------------------
Number of
Hours Costs respondents Respondent types
----------------------------------------------------------------------------------------------------------------
Total for All (Reporting & 364,495 $14,416,897 51,091 Certifying agents,
Recordkeeping). certified operations,
inspectors, and foreign
governments.
All Reporting..................... 318,859 12,454,097 51,091 Certifying agents,
certified operations,
inspectors, and foreign
governments.
All Recordkeeping................. 45,636 1,962,800 50,811 Certifying agents,
certified operations,
and foreign
governments.
----------------------------------------------------------------------------------------------------------------
Just Domestic--All (Reporting & 172,193 7,934,528 30,123 Certifying agents,
Recordkeeping). certified operations,
and inspectors.
Just Domestic Reporting........... 145,315 6,627,301 30,123 Certifying agents,
certified operations,
and inspectors.
Just Domestic Recordkeeping....... 26,878 1,307,227 29,975 Certifying agents and
certified operations.
----------------------------------------------------------------------------------------------------------------
Just Foreign--All (Reporting & 192,301 6,482,369 20,968 Certifying agents,
Recordkeeping). certified operations,
inspectors, and foreign
governments.
Just Foreign Reporting............ 173,543 5,826,795 20,968 Certifying agents,
certified operations,
inspectors, and foreign
governments.
Just Foreign Recordkeeping........ 18,758 655,573 20,836 Certifying agents,
certified operations,
and foreign
governments.
----------------------------------------------------------------------------------------------------------------
E. Executive Order 13175
Executive Order 13175 requires Federal agencies to consult and
coordinate with Tribes on a government-to-government basis on policies
that have Tribal implications, including regulations, legislative
comments, or proposed legislation. Additionally, other policy
statements or actions that have substantial direct effects on one or
more Indian Tribes, the relationship between the Federal Government and
Indian Tribes, or on the distribution of power and responsibilities
between the Federal Government and Indian Tribes also require
consultation.
AMS hosted a virtual tribal listening session on April 9, 2020, to
discuss the Strengthening Organic Enforcement proposed rule and
upcoming public comment opportunity. AMS has not received comments from
Tribes during the rulemaking process. AMS conducted an analysis of
possible Tribal impacts and determined that any impact is most likely
to be positive. AMS finds oversight protections and fraud deterrence
actions that will have positive benefits for organic producers extend
to any Tribal organic producers. Further, the specific provisions
related to grower groups may benefit small producers in a Tribe who
wish to join together under a shared certification for market
development purposes.
If a tribe requests consultation in the future, AMS will work with
the Office of Tribal Relations to ensure meaningful consultation is
provided. AMS also stands ready to provide technical assistance to
Tribes and operators wishing to participate in the organic
certification process.
F. Executive Order 13132
Executive Order 13132 mandates that federal agencies consider how
their policymaking and regulatory activities impact the policymaking
discretion of States and local officials and how well such efforts
conform to the principles of federalism defined in said order. This
executive order only pertains to regulations with clear federalism
implications.
AMS has determined that this rulemaking conforms with the
principles of federalism described in E.O. 13132. The rule does not
impose substantial direct costs or effects on States, does not alter
the relationship between States and the federal government, and does
not alter the distribution of powers and responsibilities among the
various levels of government. States had the opportunity to comment on
the proposed rule. No States provided public comment on the federalism
implications of this rule. Therefore, AMS has concluded that this
rulemaking does not have federalism implications.
G. Civil Rights Impact Analysis
AMS has reviewed this rulemaking in accordance with the Department
Regulation 4300-4, Civil Rights Impact Analysis, to address any major
civil rights impacts the rule might have on minorities, women, and
persons with disabilities. After a careful review of the rule's intent
and provisions, AMS determined that this rule will affect certifying
agents and organic inspectors, handlers of organic products, and
organic producers. AMS also determined that this rule has no
[[Page 3620]]
potential for affecting producers, handlers, certifying agents, or
inspectors in protected groups differently than the general population
of producers, handlers, certifying agents, or inspectors.
Protected individuals have the same opportunity to participate in
NOP as non-protected individuals. The USDA organic regulations prohibit
discrimination by certifying agents. Specifically, Sec. 205.501(d) of
the current regulations for accreditation of certifying agents provides
that ``No private or governmental entity accredited as a certifying
agent under this subpart shall exclude from participation in or deny
the benefits of NOP to any person due to discrimination because of
race, color, national origin, gender, religion, age, disability,
political beliefs, sexual orientation, or marital or family status.''
Section 205.501(a)(2) requires ``certifying agents to demonstrate the
ability to fully comply with the requirements for accreditation set
forth in this subpart'' including the prohibition on discrimination.
The granting of accreditation to certifying agents under Sec. 205.506
requires the review of information submitted by the certifying agent
and an on-site review of the certifying agent's client operation.
Further, if certification is denied, Sec. 205.405(d) requires that the
certifying agent notify the applicant of their right to file an appeal
to the AMS Administrator in accordance with Sec. 205.681.
These regulations provide protections against discrimination,
thereby permitting all producers, regardless of race, color, national
origin, gender, religion, age, disability, political beliefs, sexual
orientation, or marital or family status, who voluntarily choose to
adhere to the rule and qualify, to be certified as meeting NOP
requirements by an accredited certifying agent. This action in no way
changes any of these protections against discrimination.
H. Related Documents
Documents related to this rule include the Organic Foods Production
Act of 1990, as amended, (7 U.S.C. 6501-6524) and its implementing
regulations (7 CFR part 205). On August 5, 2020, AMS published the
proposed rule (85 FR 47536) to notify the public of and request
comments on the potential changes to the organic regulations discussed
in this rulemaking.
List of Subjects in 7 CFR Part 205
Administrative practice and procedure, Agricultrual Commodities,
Agriculture, Animals, Archives and records, Fees, Imports, Labeling,
Livestock, Organically produced products, Plants, Reporting and
recordkeeping requirements, Seals and insignia, Soil conservation.
For the reasons set forth in the preamble, the Agricultural
Marketing Service amends 7 CFR part 205 as follows:
PART 205--NATIONAL ORGANIC PROGRAM
0
1. The authority citation for part 205 continues to read as follows:
Authority: 7 U.S.C. 6501-6524.
0
2. Section 205.2 is amended by:
0
a. Adding in alphabetical order the terms ``Adverse action'',
``Certification activity'', ``Certification office'', ``Certification
review'', and ``Conformity assessment system'';
0
b. Revising the terms ``Handle'', ``Handler'', and ``Handling
operation'';
0
c. Adding in alphabetical order the terms ``Internal control system'',
``Organic exporter'', ``Organic fraud'', ``Organic importer'',
``Organic Integrity Database'', ``Producer group member'', ``Producer
group operation'', ``Producer group production unit'', and ``Retail
establishment'';
0
d. Removing the terms ``Retail food establishment''; and
0
e. Adding in alphabetical order the terms ``Supply chain traceability
audit'', ``Technical requirements'', and ``Unannounced inspection''.
The revisions and additions read as follows:
Sec. 205.2 Terms defined.
* * * * *
Adverse action. A noncompliance decision that adversely affects
certification, accreditation, or a person subject to the Act, including
a proposed suspension or revocation; a denial of certification,
accreditation, or reinstatement; a cease and desist notice; or a civil
penalty.
* * * * *
Certification activity. Any business conducted by a certifying
agent, or by a person acting on behalf of a certifying agent, including
but not limited to: certification management; administration;
application review; inspection planning; inspections; sampling;
inspection report review; material review; label review; records
retention; compliance review; investigating complaints and taking
adverse actions; certification decisions; and issuing transaction
certificates.
Certification office. Any site or facility where certification
activities are conducted, except for certification activities that
occur at certified operations or applicants for certification, such as
inspections and sampling.
* * * * *
Certification review. The act of reviewing and evaluating a
certified operation or applicant for certification and determining
compliance or ability to comply with the USDA organic regulations. This
does not include performing an inspection.
* * * * *
Conformity assessment system. All activities, including oversight,
accreditation, compliance review, and enforcement, undertaken by a
government to ensure that the applicable technical requirements for the
production and handling of organic agricultural products are fully and
consistently applied.
* * * * *
Handle. To sell, process, or package agricultural products,
including but not limited to trading, facilitating sale or trade on
behalf of a seller or oneself, importing to the United States,
exporting for sale in the United States, combining, aggregating,
culling, conditioning, treating, packing, containerizing, repackaging,
labeling, storing, receiving, or loading.
Handler. Any person that handles agricultural products, except
final retailers of agricultural products that do not process
agricultural products.
Handling operation. Any operation that handles agricultural
products, except final retailers of agricultural products that do not
process agricultural products.
* * * * *
Internal control system. An internal quality management system that
establishes and governs the review, monitoring, training, and
inspection of the producer group operation, and the procurement and
distribution of shared production and handling inputs and resources, to
maintain compliance with the USDA organic regulations.
* * * * *
Organic exporter. The final certified exporter of the organic
agricultural product, who facilitates the trade of, consigns, or
arranges for the transport/shipping of the organic agricultural product
from a foreign country to the United States.
Organic fraud. Deceptive representation, sale, or labeling of
nonorganic agricultural products or ingredients as ``100 percent
organic,'' ``organic,'' or ``made with organic (specified ingredients
or food group(s)).''
[[Page 3621]]
Organic importer. The operation responsible for accepting imported
organic agricultural products within the United States and ensuring NOP
Import Certificate data are entered into the U.S. Customs and Border
Protection import system of record.
Organic Integrity Database. The National Organic Program's
electronic, web-based reporting tool for the submission of data,
completion of certificates of organic operation, and other information,
or the tool's successors.
* * * * *
Producer group member. An individual engaged in the activity of
producing or harvesting agricultural products as a member of a producer
group operation.
Producer group operation. A producer, organized as a person,
consisting of producer group members and production units in geographic
proximity governed by an internal control system under one organic
system plan and certification.
Producer group production unit. A defined subgroup of producer
group members in geographic proximity within a single producer group
operation that use shared practices and resources to produce similar
agricultural products.
* * * * *
Retail establishment. Restaurants, delicatessens, bakeries, grocery
stores, or any retail business with a restaurant, delicatessen, bakery,
salad bar, bulk food self-service station, or other eat-in, carry-out,
mail-order, or delivery service of raw or processed agricultural
products.
* * * * *
Supply chain traceability audit. The process of identifying and
tracking the movement, sale, custody, handling, and organic status of
an agricultural product along a supply chain to verify the agricultural
product's compliance with this part.
* * * * *
Technical requirements. A system of relevant laws, regulations,
regulatory practices, standards, policies, and procedures that address
the certification, production, and handling of organic agricultural
products.
* * * * *
Unannounced inspection. The act of examining and evaluating all or
a portion of the production or handling activities of a certified
operation without advance notice to determine compliance with the Act
and the regulations in this part.
* * * * *
0
3. Section 205.100 is amended by revising paragraph (a) and paragraph
(c) introductory text to read as follows:
Sec. 205.100 What has to be certified.
(a) Except for the exempt operations described in Sec. 205.101,
each operation or portion of an operation that produces or handles
agricultural products intended to be sold, labeled, or represented as
``100 percent organic,'' ``organic,'' or ``made with organic (specified
ingredients or food group(s))'' must be certified according to the
provisions of subpart E of this part and must meet all other applicable
requirements of this part.
* * * * *
(c) Any person or responsibly connected person that:
* * * * *
0
4. Revise Sec. 205.101 to read as follows:
Sec. 205.101 Exemptions from certification.
The following operations in paragraphs (a) through (h) of this
section are exempt from certification under subpart E of this part and
from submitting an organic system plan for acceptance or approval under
Sec. 205.201 but must comply with the applicable organic production
and handling requirements of subpart C of this part, the applicable
labeling requirements of subpart D of this part, and any requirements
described in paragraphs (a) through (i) of this section.
(a) A production or handling operation that sells agricultural
products as ``organic'' but whose gross agricultural income from
organic sales totals $5,000 or less annually.
(b) A retail establishment that does not process organically
produced agricultural products.
(c) A retail establishment that processes, at the point of final
sale, agricultural products certified under this part as ``100 percent
organic,'' ``organic,'' or ``made with organic (specified ingredients
or food group(s)).''
(d) A handling operation that only handles agricultural products
that contain less than 70 percent organic ingredients (as described in
Sec. 205.301(d)) or that only identifies organic ingredients on the
information panel.
(e) An operation that only receives, stores, and/or prepares for
shipment, but does not otherwise handle, organic agricultural products
that:
(1) Are enclosed in sealed, tamper-evident packages or containers
prior to being received or acquired by the operation; and
(2) Remain in the same sealed, tamper-evident packages or
containers and are not otherwise handled while in the control of the
operation.
(f) An operation that only buys, sells, receives, stores, and/or
prepares for shipment, but does not otherwise handle, organic
agricultural products already labeled for retail sale that:
(1) Are enclosed in sealed, tamper-evident packages or containers
that are labeled for retail sale prior to being received or acquired by
the operation; and
(2) Remain in the same sealed, tamper-evident packages or
containers that are labeled for retail sale and are not otherwise
handled while in the control of the operation.
(g) A Customs broker (per 19 CFR 111.1) that only conducts customs
business but does not otherwise handle organic agricultural products.
(h) An operation that only arranges for the shipping, storing,
transport, or movement of organic agricultural products but does not
otherwise handle organic products.
(i) Recordkeeping by exempt operations.
(1) Exempt operations described in paragraphs (a) and (c) through
(f) of this section must make available to representatives of the
Secretary, upon request, records that:
(i) Demonstrate that agricultural products identified as organic
were organically produced and handled; and
(ii) Verify quantities of organic agricultural products received
and shipped or sold
(2) All records described in this section must be maintained for no
less than 3 years beyond their creation, and the operations must allow
representatives of the Secretary and the applicable State organic
programs' governing State official access to these records for
inspection and copying during normal business hours to determine
compliance with the applicable regulations set forth in this part.
0
5. Section 205.103 is amended by:
0
a. Revising paragraph (b)(2);
0
b. Redesignating paragraphs (b)(3) and (4) as paragraphs (b)(4) and
(5); and
0
c. Adding new paragraph (b)(3).
The revision and addition read as follows:
Sec. 205.103 Recordkeeping by certified operations.
* * * * *
(b) * * *
(2) Fully disclose all activities and transactions of the certified
operation, in sufficient detail as to be readily understood and
audited; records must span the time of purchase or acquisition, through
production, to sale
[[Page 3622]]
or transport and be traceable back to the last certified operation;
(3) Include audit trail documentation for agricultural products
handled or produced by the certified operation and identify
agricultural products on these records as ``100% organic,''
``organic,'' or ``made with organic (specified ingredients or food
group(s)),'' or similar terms, as applicable;
* * * * *
0
6. Section 205.201 is amended by:
0
a. Removing the words ``or excluded'' in paragraph (a) introductory
text;
0
b. Revising paragraph (a)(3); and
0
c. Adding paragraph (c).
The revision and addition to read as follows:
Sec. 205.201 Organic production and handling system plan.
(a) * * *
(3) A description of the monitoring practices and procedures to be
performed and maintained, including the frequency with which they will
be performed, to verify that the plan is effectively implemented. This
must include a description of the monitoring practices and procedures
to verify suppliers in the supply chain and organic status of
agricultural products received, and to prevent organic fraud, as
appropriate to the certified operation's activities, scope, and
complexity;
* * * * *
(c) In addition to paragraph (a) of this section, a producer group
operation's organic system plan must describe its internal control
system. The description of the internal control system must:
(1) Define the organizational structure, roles, and
responsibilities of all personnel;
(2) Identify producer group production units and locations;
(3) Describe measures to protect against potential conflicts of
interest and protect internal control system personnel from
retribution;
(4) Define geographic proximity criteria for producer group members
and producer group production units;
(5) Describe procedures for accepting new members into the producer
group operation, including initial inspection and compliance
determination;
(6) Describe characteristics of high-risk producer group members
and producer group production units;
(7) Describe how shared resources, including production practices
and inputs, are procured and provided to all producer group members and
personnel;
(8) Describe how training, education, and technical assistance is
provided to producer group members and internal control system
personnel;
(9) Describe the system of records used to demonstrate compliance
with this part, including traceability and mass-balance audits; and
(10) Describe how internal monitoring, surveillance, inspection,
sanctions, and auditing are used to assess the compliance of all
producer group members.
0
7. Add Sec. 205.273 to subpart C to read as follows:
Sec. 205.273 Imports to the United States.
Each shipment of organic agricultural products imported into the
United States must be certified pursuant to subpart E of this part,
labeled pursuant to subpart D of this part, be declared as organic to
U.S. Customs and Border Protection, and be associated with valid NOP
Import Certificate data.
(a) Persons exporting organic agricultural products to the United
States must request an NOP Import Certificate from a certifying agent
prior to their export. Only certifying agents accredited by the USDA or
foreign certifying agents authorized under an organic trade arrangement
or agreement may issue an NOP Import Certificate.
(b) The certifying agent must review an NOP Import Certificate
request and determine whether the export complies with the USDA organic
regulations. The certifying agent must have and implement a documented
organic control system for intaking and approving or rejecting the
validity of an NOP Import Certificate request. The certifying agent
shall issue the NOP Import Certificate through the Organic Integrity
Database only if the export complies with the USDA organic regulations.
(c) Each compliant organic import must be declared as organic to
U.S. Customs and Border Protection by entering NOP Import Certificate
data into the U.S. Customs and Border Protection's Automated Commercial
Environment system. Organic imports must be clearly identified and
marked as organic on all import documents including but not limited to
invoices, packing lists, bills of lading, and U.S. Customs and Border
Protection entry data. Only NOP Import Certificate data generated by
the Organic Integrity Database are valid.
(d) Upon receiving a shipment with organic agricultural products,
the organic importer must ensure the import is accompanied by accurate
NOP Import Certificate data and must verify that the shipment has had
no contact with prohibited substances pursuant to Sec. 205.272 or
exposure to ionizing radiation pursuant to Sec. 205.105, since export.
The organic importer must have a documented organic control system to
conduct this verification.
0
8. Amend Sec. 205.300 by revising paragraph (c) to read as follows:
Sec. 205.300 Use of the term, ``organic.''
* * * * *
(c) Products produced in a foreign country and exported for sale in
the United States must be certified pursuant to subpart E of this part,
labeled pursuant to this subpart D, and must comply with the
requirements in Sec. 205.273.
* * * * *
0
9. Amend Sec. 205.301 by revising paragraphs (f)(2) and (3) to read as
follows:
Sec. 205.301 Product composition.
* * * * *
(f) * * *
(2) Be processed using ionizing radiation, pursuant to Sec.
205.105(f);
(3) Be produced using sewage sludge, pursuant to Sec. 205.105(g);
* * * * *
0
10. Amend Sec. 205.302 by revising paragraphs (a)(1) through (3) to
read as follows:
Sec. 205.302 Calculating the percentage of organically produced
ingredients.
(a) * * *
(1) Dividing the total net weight of the combined organic
ingredients at formulation by the total weight of all ingredients of
the product at formulation. Water and salt added as ingredients at
formulation are excluded from the calculation.
(2) Dividing the total fluid volume of the combined organic
ingredients at formulation by the total fluid volume of all ingredients
of the product at formulation if the product and ingredients are
liquid. Water and salt added as ingredients at formulation are excluded
from the calculation. If the liquid product is identified on the
principal display panel or information panel as being reconstituted
from concentrates, the calculation should be made based on single-
strength concentrations of all ingredients.
(3) For products containing organically produced ingredients in
both solid and liquid form, dividing the combined net weight of the
solid organic ingredients and the net weight of the liquid organic
ingredients at formulation by the total weight of all ingredients of
the product at formulation. Water and salt added as ingredients at
formulation are excluded from the calculation.
* * * * *
0
11. Revise Sec. 205.307 to read as follows:
[[Page 3623]]
Sec. 205.307 Labeling of nonretail containers.
(a) Nonretail containers used to ship or store certified organic
agricultural products must display:
(1) Identification of the product as organic; and
(2) The production lot number, shipping identification, or other
unique information that links the container to audit trail
documentation.
(b) Audit trail documentation for nonretail containers must
identify the last certified operation that handled the agricultural
product.
(c) Paragraph (a)(1) of this section does not apply to nonretail
containers used to ship or store agricultural products packaged for
retail sale with organic identification visible on the retail label.
(d) Shipping containers of domestically produced product labeled as
organic intended for export to international markets may be labeled in
accordance with any shipping container labeling requirements of the
foreign country of destination or the container labeling specifications
of a foreign contract buyer: Provided, that, the shipping containers
and shipping documents accompanying such organic products are clearly
marked ``For Export Only'' and: Provided further, that proof of such
container marking and export must be maintained by the handler in
accordance with recordkeeping requirements for exempt operations under
Sec. 205.101.
0
12. Section 205.310 is amended by revising the section heading and
paragraphs (a) and (b) to read as follows:
Sec. 205.310 Agricultural products produced or processed by an exempt
operation.
(a) An agricultural product organically produced or processed by an
exempt operation must not:
(1) Display the USDA seal or any certifying agent's seal or other
identifying mark which represents the exempt operation as a certified
organic operation; or
(2) Be represented as a certified organic product or certified
organic ingredient to any buyer.
(b) An agricultural product organically produced or processed by an
exempt operation may be identified as an organic product or organic
ingredient in a multi-ingredient product produced by the exempt
operation. Such product or ingredient must not be identified or
represented as ``organic'' in a product processed by others.
* * * * *
0
13. Section 205.400 is amended by:
0
a. Removing ``Sec. 205.200'' and adding in its place ``Sec. 205.201''
in paragraph (b); and
0
b. Adding paragraph (g).
The addition reads as follows:
Sec. 205.400 General requirements for certification.
* * * * *
(g) In addition to paragraphs (a) through (f) of this section, a
producer group operation must:
(1) Be organized as a person;
(2) Use centralized processing, distribution, and marketing
facilities and systems;
(3) Be organized into producer group production units;
(4) Maintain an internal control system to implement the practices
described in Sec. 205.201(c) and ensure compliance with this part;
(5) Ensure that all agricultural products sold, labeled, or
represented as organic are produced only by producer group members
using land and facilities within the certified operation;
(6) Ensure that producer group members do not sell, label, or
represent their agricultural products as organic outside of the
producer group operation unless they are individually certified;
(7) Report to the certifying agent, at least annually, the name and
location of all producer group members and producer group production
units, the agricultural products produced, estimated yields, and size
of production areas;
(8) Conduct internal inspections of each producer group member, at
least annually, by internal inspectors with the member present, which
must include mass-balance audits and reconciliation of each producer
group member's and each producer group production unit's yield and
group sales;
(9) Implement recordkeeping requirements to ensure traceability
from production at each producer group member and production unit
through handling to sale and transport;
(10) Implement procedures to ensure all production and handling by
the producer group operation is compliant with the USDA organic
regulations and the Act; and
(11) Address any other terms or conditions determined by the
Administrator to be necessary to enforce compliance with the USDA
organic regulations and the Act.
Sec. 205.401 [Amended]
0
14. Amend Sec. 205.401 in paragraph (a) by removing ``Sec. 205.200''
and adding in its place ``Sec. 205.201''.
0
15. Section 205.403 is amended by:
0
a. Redesignating paragraph (a)(2) as paragraph (a)(3);
0
b. Adding new paragraph (a)(2);
0
c. Redesignating paragraphs (b) through (e) as paragraphs (c) through
(f);
0
d. Adding new paragraph (b);
0
e. In newly redesignated paragraph (d)(2), removing ``Sec. 205.200''
and adding in its place ``Sec. 205.201''; and
0
f. Adding paragraphs (d)(4) and (5).
The additions read as follows:
Sec. 205.403 On-site inspections.
(a) * * *
(2) Inspections of a producer group operation must:
(i) Assess the internal control system's compliance, or ability to
comply, with the requirements of Sec. 205.400(g)(8). This must include
review of the internal inspections conducted by the internal control
system.
(ii) Conduct witness audits of internal control system inspectors
performing inspections of the producer group operation.
(iii) Individually inspect at least 1.4 times the square root or 2%
of the total number of producer group members, whichever is higher. All
producer group members determined to be high risk by the certifying
agent must be inspected. At least one producer group member in each
producer group production unit must be inspected.
(iv) Inspect each handling facility.
* * * * *
(b) Unannounced inspections. (1) A certifying agent must, on an
annual basis, conduct unannounced inspections of a minimum of five
percent of the operations it certifies, rounded up to the nearest whole
number.
(2) Certifying agents must be able to conduct unannounced
inspections of any operation they certify and must not accept
applications or continue certification with operations located in areas
where they are unable to conduct unannounced inspections.
* * * * *
(d) * * *
(4) Mass-balances, in that quantities of organic product and
ingredients produced or purchased account for organic product and
ingredients used, stored, sold, or transported (that is, inputs account
for outputs); and
(5) That organic products and ingredients are traceable by the
operation from the time of purchase or acquisition through production
to sale or transport; and that the certifying agent can verify
compliance back to the last certified operation.
* * * * *
0
16. Section Sec. 205.404 is amended by revising paragraph (b),
redesignating paragraph (c) as paragraph (d), and adding a new
paragraph (c).
The revision and addition read as follows:
[[Page 3624]]
Sec. 205.404 Certificates of organic operation.
* * * * *
(b) The certifying agent must issue a certificate of organic
operation. The certificate of organic operation must be generated from
the Organic Integrity Database and may be provided to certified
operations electronically.
(c) In addition to the certificate of organic operation provided
for in paragraph (b) of this section, a certifying agent may issue its
own addenda to the certificate of organic operation. If issued, any
addenda must include:
(1) Name, address, and contact information for the certified
operation;
(2) The certified operation's unique ID number/code that
corresponds to the certified operation's ID number/code in the Organic
Integrity Database;
(3) A link to the Organic Integrity Database or a link to the
certified operation's profile in the Organic Integrity Database, along
with a statement, ``You may verify the certification of this operation
at the Organic Integrity Database,'' or a similar statement;
(4) Name, address, and contact information of the certifying agent;
and
(5) ``Addendum issue date.''
* * * * *
Sec. 205.405 [Amended]
0
17. Amend Sec. 205.405 by removing paragraph (c)(3).
0
18. Amend 205.406 by revising paragraphs (a) and (b) to read as
follows:
Sec. 205.406 Continuation of certification.
(a) To continue certification, a certified operation must annually
pay the certification fees and submit the following information to the
certifying agent:
(1) A summary statement, supported by documentation, detailing any
deviations from, changes to, modifications to, or other amendments made
to the organic system plan submitted during the previous year;
(2) Any additions or deletions to the previous year's organic
system plan, intended to be undertaken in the coming year, detailed
pursuant to Sec. 205.201;
(3) Any additions to or deletions from the information required
pursuant to Sec. 205.401(b); and
(4) Other information as deemed necessary by the certifying agent
to determine compliance with the Act and the regulations in this part.
(b) The certifying agent must arrange and conduct an on-site
inspection, pursuant to Sec. 205.403, of the certified operation at
least once per calendar year.
* * * * *
Sec. 205.500 [Amended]
0
19. Amend Sec. 205.500 by removing paragraph (c).
0
20. Section 205.501 is amended by:
0
a. Revising paragraphs (a)(4), (5), (6), (10), (13), and (15);
0
b. Redesignating paragraph (a)(21) as paragraph (a)(23); and
0
c. Adding new paragraph (a)(21) and paragraph (a)(22).
The revisions and additions read as follows:
Sec. 205.501 General requirements for accreditation.
(a) * * *
(4) Continuously use a sufficient number of qualified and
adequately trained personnel, including inspectors and certification
review personnel, to comply with and implement the USDA organic
standards.
(i) Certifying agents must demonstrate that all inspectors,
including staff, volunteers, and contractors, have the relevant
knowledge, skills, and experience required to inspect operations of the
scope and complexity assigned and to evaluate compliance with the
applicable regulations of this part.
(A) Certifying agents must demonstrate that inspectors continuously
maintain adequate knowledge and skills about the current USDA organic
standards, production and handling practices, certification and
inspection, import and/or export requirements, traceability audits,
mass-balance audits, written and oral communication skills, sample
collection, investigation techniques, and preparation of technically
accurate inspection documents.
(B) All inspectors must demonstrate successful completion of
training that is relevant to inspection. Inspectors with less than one
year of inspection experience must complete at least 50 hours of
training within their first year and prior to performing inspections
independently. Inspectors with one or more years of inspection
experience must annually complete at least 10 hours of training if
inspecting one area of operation (as defined at Sec. 205.2) and an
additional 5 hours of training for each additional area of operation
inspected.
(C) Certifying agents must demonstrate that inspectors have a
minimum of 2,000 hours of experience relevant to the scope and
complexity of operations they will inspect before assigning initial
inspection responsibilities.
(ii) Certifying agents must demonstrate that all certification
review personnel, including staff, volunteers, or contractors, have the
knowledge, skills, and experience required to perform certification
review of operations of the scope and complexity assigned and to
evaluate compliance with the applicable regulations of this part.
(A) Certifying agents must demonstrate that all certification
review personnel continuously maintain adequate knowledge and skills in
the current USDA organic standards, certification and compliance
processes, traceability audits, mass-balance audits, and practices
applicable to the type, volume, and range of review activities
assigned.
(B) All certification review personnel must demonstrate successful
completion of training that is relevant to certification review.
Certification review personnel with less than one year of certification
review experience must complete at least 50 hours of training within
their first year performing certification review. Certification review
personnel with one or more years of certification review experience
must annually complete at least 10 hours of training if conducting
certification review related to one area of operation and an additional
5 hours of training for each additional area of operation.
(iii) Certifying agents must maintain current training
requirements, training procedures, and training records for all
inspectors and certification review personnel.
(5) Demonstrate that all persons with inspection or certification
review responsibilities have sufficient expertise in organic production
or handling techniques to successfully perform the duties assigned.
Sufficient expertise must include knowledge of certification to USDA
organic standards and evidence of education, training, or professional
experience in the fields of agriculture, science, or organic production
and handling that relates to assigned duties.
(6) Conduct an annual performance evaluation of all persons who
conduct inspections, certification review, or implement measures to
correct any deficiencies in certification services.
(i) Witness inspections--certifying agents must ensure that each
inspector is evaluated while performing an inspection at least once
every three years, or more frequently if warranted. Inspectors with
less than three years of inspection experience must undergo a witness
inspection annually. Witness inspections must be performed by
certifying agent personnel who are qualified to evaluate inspectors.
(ii) Certifying agents must maintain documented policies,
procedures, and
[[Page 3625]]
records for annual performance evaluations and witness inspections.
* * * * *
(10) Maintain strict confidentiality with respect to its clients
under the applicable organic certification program and not disclose to
third parties (except for the Secretary or the applicable State organic
program's governing State official or their authorized representatives)
any business-related information concerning any client obtained while
implementing the regulations in this part, except:
(i) For information that must be made available to any member of
the public, as provided for in Sec. 205.504(b)(5);
(ii) For enforcement purposes, certifying agents must exchange any
compliance-related information that is credibly needed to certify,
decertify, or investigate an operation, including for the purpose of
verifying supply chain traceability and audit trail documentation; and
(iii) If a certified operation's proprietary business information
is compliance-related and thus credibly needed to certify, decertify,
or investigate that operation, certifying agents may exchange that
information for the purposes of enforcing the Act, but the information
in question still retains its proprietary character even after it is
exchanged and all of the certifying agents that are involved in the
exchange still have a duty to preserve the confidentiality of that
information after the exchange.
* * * * *
(13) Accept the certification decisions made by another certifying
agent accredited or accepted by USDA pursuant to Sec. 205.500.
Certifying agents must provide information to other certifying agents
to ensure organic integrity or to enforce organic regulations,
including to verify supply chain integrity, authenticate the organic
status of certified products, and conduct investigations;
* * * * *
(15) Maintain current and accurate data in the Organic Integrity
Database for each operation which it certifies;
* * * * *
(21) Conduct risk-based supply chain traceability audits as
described in the criteria and procedures for supply chain audits, per
Sec. 205.504(b)(7), and share audit findings with other certifying
agents as needed to determine compliance, per paragraph (a)(13) of this
section.
(22) Notify AMS not later than 90 calendar days after certification
activities begin in a new certification office. The notification must
include the countries where the certification activities are being
provided, the nature of the certification activities, and the
qualifications of the personnel providing the certification activities.
* * * * *
0
21. Section 205.504 is amended by revising the introductory text and
paragraph (b)(4) and adding paragraphs (b)(7) and (8) to read as
follows:
Sec. 205.504 Evidence of expertise and ability.
A private or governmental entity seeking accreditation as a
certifying agent must submit the following documents and information to
demonstrate its expertise in organic production or handling techniques;
its ability to fully comply with and implement the organic
certification program established in Sec. Sec. 205.100 and 205.101,
205.201 through 205.203, 205.300 through 205.303, 205.400 through
205.406, and 205.661 through 205.663; and its ability to comply with
the requirements for accreditation set forth in Sec. 205.501:
* * * * *
(b) * * *
(4) A copy of the procedures to be used for sharing information
with other certifying agents and for maintaining the confidentiality of
any business-related information as set forth in Sec. 205.501(a)(10);
* * * * *
(7) A copy of the criteria to identify high-risk operations and
agricultural products for supply chain traceability audits; and
procedures to conduct risk-based supply chain traceability audits, as
required in Sec. 205.501(a)(21); and procedures to report credible
evidence of organic fraud to the Administrator.
(8) A copy of reasonable decision criteria for acceptance of
mediation, and a process for identifying personnel conducting mediation
and setting up mediation.
* * * * *
0
22. Add Sec. 205.511 to subpart F to read as follows:
Sec. 205.511 Accepting foreign conformity assessment systems.
(a) Foreign product may be certified under the USDA organic
regulations by a USDA-accredited certifying agent and imported for sale
in the United States. Foreign product that is produced and handled
under another country's organic certification program may be sold,
labeled, or represented in the United States as organically produced if
the U.S. Government determines that such country's organic
certification program provides technical requirements and a conformity
assessment system governing the production and handling of such
products that are at least equivalent to the requirements of the Act
and the regulations in this part.
(b) Countries desiring to establish eligibility of product
certified under that country's organic certification program to be
sold, labeled, or represented in the United States as organically
produced may request equivalence determinations from AMS. A foreign
government must maintain compliance and enforcement mechanisms to
ensure that its organic certification program is fully meeting the
terms and conditions of any equivalence determination provided by the
U.S. Government pursuant to this section. To request an equivalence
determination, the requesting country must submit documentation that
fully describes its technical requirements and conformity assessment
system. If the U.S. Government determines it can proceed, AMS will
assess the country's organic certification program to evaluate if it is
equivalent.
(c) USDA, working with other Federal agencies, will describe the
scope of an equivalence determination.
(d) AMS will conduct regular reviews and reassessments of countries
deemed equivalent to verify that the foreign government's technical
requirements and conformity assessment system continue to be at least
equivalent to the requirements of the Act and the regulations of this
part, and will determine if the equivalence determination should be
continued, amended, or terminated. AMS will determine the timing and
scope of reviews and re-assessments based on, but not limited to,
factors such as: the terms of the equivalence determination, changes to
the foreign country's technical requirements or conformity assessment
system, the results of previous reviews and re-assessments, instances
of suspected or verified noncompliance issues, the volume of trade, and
other factors contributing to the risk level of the equivalence
determination.
(e) The U.S. Government may terminate an equivalence determination
if the terms or conditions established under the equivalence
determination are not met; if AMS determines that the country's
technical requirements and/or conformity assessment program are no
longer equivalent; if AMS determines that the foreign government's
organic control system is inadequate to ensure that the country's
organic certification program is fully meeting the terms and conditions
under the equivalence determination; or for other good cause.
[[Page 3626]]
0
23. Amend Sec. 205.660 by redesignating paragraphs (c) and (d) as
paragraphs (d) and (e) and adding new paragraph (c).
The addition reads as follows:
Sec. 205.660 General.
* * * * *
(c) The Program Manager may initiate enforcement action against any
person who sells, labels, or provides other market information
concerning an agricultural product if such label or information implies
that such product is produced or handled using organic methods, if the
product was produced or handled in violation of the Organic Foods
Production Act or the regulations in this part.
* * * * *
0
24. Amend Sec. 205.661 by revising the section heading to read as
follows:
Sec. 205.661 Investigation.
* * * * *
0
25. Section 205.662 is amended by:
0
a. Adding paragraph (e)(3);
0
b. Revising the first sentence of paragraph (f)(1); and
0
c. Revising paragraph (g)(1).
The addition and revisions read as follows:
Sec. 205.662 Noncompliance procedure for certified operations.
* * * * *
(e) * * *
(3) Within 3 business days of issuing a notification of suspension
or revocation, or the effective date of an operation's surrender, the
certifying agent must update the operation's status in the Organic
Integrity Database.
(f) * * *
(1) A certified operation or a person responsibly connected with an
operation whose certification has been suspended may at any time,
unless otherwise stated in the notification of suspension, submit a
request to the Secretary for reinstatement of its certification, or
submit a request for eligibility to be certified. * * *
* * * * *
(g) * * *
(1) Knowingly sells or labels a product as organic, except in
accordance with the Act, shall be subject to a civil penalty of not
more than the amount specified in 7 CFR 3.91(b)(1)(xxxvi) per
violation.
* * * * *
0
26. Revise Sec. 205.663 to read as follows:
Sec. 205.663 Mediation.
(a) A certifying agent must submit with its administrative policies
and procedures: decision criteria for acceptance of mediation, and a
process for identifying personnel conducting mediation and setting up
mediation sessions per Sec. 205.504(b)(8).
(b) A certified operation or applicant for certification may
request mediation to resolve a denial of certification or proposed
suspension or proposed revocation of certification issued by a
certifying agent or State organic program.
(1) A certified operation or applicant for certification must
submit any request for mediation in writing to the applicable
certifying agent or State organic program within 30 calendar days of
receipt of the notice of proposed suspension or proposed revocation of
certification or denial of certification.
(2) A certifying agent or State organic program may accept or
reject a request for mediation based on the decision criteria required
in paragraph (a) of this section. Certifying agents must document these
criteria and how the certifying agent applied the criteria to the
request.
(3) If a certifying agent rejects a mediation request, it must
provide this rejection, and the justification for the rejection, in
writing to the applicant for certification or certified operation. The
rejection must include the right to request an appeal, pursuant to
Sec. 205.681, within 30 calendar days of the date of receipt of the
written notification of rejection of the request for mediation.
(4) When an operation appeals a rejection of mediation, the adverse
action which is contested must not be finalized during the appeal
proceeding.
(c) Both parties must agree on the person conducting the mediation.
(d) If a State organic program is in effect, the parties must
follow the mediation procedures established in the State organic
program and approved by the Secretary.
(e) The parties to the mediation have a maximum of 30 calendar days
from the start of mediation to reach an agreement. Successful mediation
results in a settlement agreement agreed to in writing by both the
certifying agent and the certified operation. If mediation is
unsuccessful, the applicant for certification or certified operation
has 30 calendar days from receipt of a written notice of termination of
mediation to appeal the denial of certification or proposed suspension
or revocation pursuant to Sec. 205.681.
(f) Any settlement agreement reached through mediation must comply
with the Act and the regulations in this part. The Program Manager may
review any mediated settlement agreement for conformity to the Act and
the regulations in this part and may reject any agreement or provision
not in conformance with the Act or the regulations in this part.
(g) The Program Manager may propose mediation and enter into a
settlement agreement at any time to resolve any adverse action notice.
0
27. Amend Sec. 205.665 by revising paragraph (a) to read as follows:
Sec. 205.665 Noncompliance procedure for certifying agents.
(a) Notification. (1) A written notification of noncompliance will
be sent to the certifying agent when:
(i) An inspection, review, or investigation of an accredited
certifying agent by the Program Manager reveals any noncompliance with
the Act or regulations in this part; or
(ii) The Program Manager determines that the certification
activities of the certifying agent, or any person performing
certification activities on behalf of the certifying agent, are not
compliant with the Act or the regulations in this part; or
(iii) The Program Manager determines that the certification
activities at a certification office, and/in specific countries, are
not compliant with the Act or the regulations in this part.
(2) Such notification must provide:
(i) A description of each noncompliance;
(ii) The facts upon which the notification of noncompliance is
based; and
(iii) The date by which the certifying agent must rebut or correct
each noncompliance and submit supporting documentation of each
correction when correction is possible.
* * * * *
0
28. Revise Sec. 205.680 to read as follows:
Sec. 205.680 General.
(a) Persons subject to the Act who believe they are adversely
affected by an adverse action of the National Organic Program's Program
Manager may appeal such decision to the Administrator.
(b) Persons subject to the Act who believe they are adversely
affected by an adverse action of a State organic program may appeal
such decision to the State organic program's governing State official,
who will initiate handling of the appeal pursuant to appeal procedures
approved by the Secretary.
(c) Persons subject to the Act who believe they are adversely
affected by an adverse action of a certifying agent may appeal such
decision to the Administrator, Except, that, when the person is subject
to an approved State
[[Page 3627]]
organic program, the appeal must be made to the State organic program.
(d) Persons subject to the Act who believe they are adversely
affected by an adverse action of a certifying agent or a State organic
program may request mediation as provided in Sec. 205.663.
(e) All appeals must comply with the procedural requirements in
Sec. 205.681(c) and (d).
(f) All written communications between parties involved in appeal
proceedings must be sent to the recipient's place of business by a
delivery service which provides dated return receipts.
(g) All appeals must be reviewed, heard, and decided by persons not
involved with the adverse action being appealed.
0
29. Amend Sec. 205.681 by revising paragraph (a) introductory text and
paragraphs (a)(2), (b), (c), and (d)(1) and (3) to read as follows:
Sec. 205.681 Appeals.
(a) Adverse actions by certifying agents. An applicant for
certification may appeal a certifying agent's notice of denial of
certification, and a certified operation may appeal a certifying
agent's notification of proposed suspension or proposed revocation of
certification to the Administrator, Except, that, when the applicant or
certified operation is subject to an approved State organic program,
the appeal must be made to the State organic program which will carry
out the appeal pursuant to the State organic program's appeal
procedures approved by the Secretary.
* * * * *
(2) If the Administrator or State organic program denies an appeal,
a formal administrative proceeding will be initiated to deny, suspend,
or revoke the certification unless the parties resolve the issues
through settlement, or the appellant waives or does not timely request
a hearing. Such proceeding must be conducted pursuant to the U.S.
Department of Agriculture's Uniform Rules of Practice, 7 CFR part 1,
subpart H, or the State organic program's rules of procedure.
(b) Adverse actions by the NOP Program Manager. A person affected
by an adverse action, as defined by Sec. 205.2, issued by the NOP
Program Manager, may appeal to the Administrator.
(1) If the Administrator sustains an appeal, an applicant will be
issued accreditation, a certifying agent will continue its
accreditation, or an operation will continue its certification, a civil
penalty will be withdrawn, and a cease and desist notice will be
withdrawn, as applicable to the operation.
(2) If the Administrator denies an appeal, a formal administrative
proceeding will be initiated to deny, suspend, or revoke the
accreditation or certification and/or levy civil penalties unless the
parties resolve the issues through settlement, the appellant waives a
hearing, or the appellant does not timely request a hearing. Such
proceeding must be conducted pursuant to the U.S. Department of
Agriculture's Uniform Rules of Practice, 7 CFR part 1, subpart H.
(c) Filing period. An appeal must be filed in writing within the
time period provided in the letter of notification or within 30 days
from receipt of the notification, whichever occurs later. The appeal
will be considered ``filed'' on the date received by the Administrator
or by the State organic program. An adverse action will become final
and nonappealable unless an appeal is timely filed.
(d) * * *
(1) Appeals to the Administrator and Requests for Hearing must be
filed in writing and addressed to: 1400 Independence Ave. SW, Room
2642, Stop 0268, Washington, DC 20250, or electronic transmission,
[email protected].
* * * * *
(3) All appeals must include a copy of the adverse action and a
statement of the appellant's reasons for believing that the action was
not proper or made in accordance with applicable program regulations.
Erin Morris,
Associate Administrator, Agricultural Marketing Service.
[FR Doc. 2023-00702 Filed 1-18-23; 8:45 am]
BILLING CODE 3410-02-P