Information From Foreign Regions Applying for Recognition of Animal Health Status, 44107-44110 [2012-18324]
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44107
Rules and Regulations
Federal Register
Vol. 77, No. 145
Friday, July 27, 2012
This section of the FEDERAL REGISTER
contains regulatory documents having general
applicability and legal effect, most of which
are keyed to and codified in the Code of
Federal Regulations, which is published under
50 titles pursuant to 44 U.S.C. 1510.
The Code of Federal Regulations is sold by
the Superintendent of Documents. Prices of
new books are listed in the first FEDERAL
REGISTER issue of each week.
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
9 CFR Part 92
[Docket No. APHIS–2007–0158]
RIN 0579–AD30
Information From Foreign Regions
Applying for Recognition of Animal
Health Status
Animal and Plant Health
Inspection Service, USDA.
ACTION: Final rule.
AGENCY:
We are amending the
regulations that govern the importation
of animals and animal products by
consolidating the list of factors APHIS
considers when evaluating the animal
health status of a foreign region and by
setting out new factors APHIS will
consider when evaluating a region as
historically free of a specific disease.
These changes will make clearer the
types of information APHIS needs from
a requesting region in order to conduct
an evaluation.
DATES: Effective Date: August 27, 2012.
FOR FURTHER INFORMATION CONTACT: Dr.
Kelly Rhodes, Regionalization
Evaluation Services, Sanitary Trade
Issues Team, National Center for Import
and Export, VS, APHIS, 4700 River
Road Unit 38, Riverdale, MD 20737–
1231; (301) 851–3300.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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Background
The regulations in 9 CFR part 92,
‘‘Importation of Animals and Animal
Products; Procedures for Requesting
Recognition of Regions’’ (referred to
below as the regulations), set forth the
process by which a foreign government
may request recognition of the animal
health status of a region.
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Section 92.2 of the regulations
requires that such requests be
accompanied by information regarding
the region that will enable the Animal
and Plant Health Inspection Service
(APHIS) of the U.S. Department of
Agriculture to evaluate the request.
On December 28, 2011, we published
in the Federal Register (76 FR 81404–
81408, Docket No. APHIS–2007–0158) a
proposal 1 to amend the regulations by
consolidating the 11 factors listed in
§ 92.2(b) that APHIS considers when
evaluating the animal health status of a
foreign region into 8 factors. We also
proposed to establish criteria for
recognizing a region as historically free
of a specific disease. Our intent was to
make clearer the types of information
APHIS needs from a requesting region to
conduct an evaluation. Additionally,
although our regulations focus on
requests from foreign regions, we noted
that APHIS could initiate an evaluation
of the disease status of a foreign region
and, if we did, would conduct the
evaluation using these same factors. We
also proposed to remove a statement in
§ 92.2(d) that supporting information
submitted with country requests will be
made available to the public prior to
initiation of rulemaking. We proposed
to replace it with a statement that a list
of regions that have requested
recognition of their animal health status
will be available to the public, and to
leave in place a statement in § 92.2(f)
that when APHIS makes its evaluation
available for public comment, the public
will have access to the information
upon which APHIS based its evaluation,
as well as the evaluation itself.
We solicited comments concerning
our proposal for 60 days ending
February 27, 2012. We received 12
comments (including two from the same
person) by that date. They were from an
organization representing pork
producers, an organization representing
cattle farmers and ranchers, an
organization representing U.S.
consumers, a wildlife conservation
society, a State board of animal health,
foreign governments, and individuals.
Six commenters supported the
proposed changes.
Three commenters objected to the
proposed rule. Two of the three said
that they oppose the concept of
1 To view the proposed rule and the comments
we received, go to https://www.regulations.gov/
#!docketDetail;D=APHIS-2007-0158.
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regionalization for animal health status.
Two also said they were concerned
about APHIS’ ability to predict
outbreaks or detect disease threats
under the current 11 factors and oppose
finalizing a rule predicated on those
factors. They cited several instances
where regions APHIS had recognized as
free of a disease had subsequently
experienced an outbreak of that disease.
One commenter also said that APHIS
should not adopt international criteria
for evaluating a region as historically
free of a disease until we have
conducted a scientific study to
determine whether such
recommendations are, in fact, capable of
adequately assessing whether a country
is historically free of a disease.
We are making no changes to the
proposed rule in response to these
comments. Regionalization is an
important principle of the World Trade
Organization Agreement on the
Application of Sanitary and
Phytosanitary Measures (WTO–SPS
Agreement). Regionalization is based on
recognition that pest and disease
conditions may vary across a country as
a result of ecological, environmental,
and epidemiological factors, and on the
premise that these differences should be
taken into account in developing
science-based regulatory measures. The
United States has successfully applied
the concept for decades in domestic
disease control and eradication
programs, and regionalization of the
United States for bluetongue and other
diseases has facilitated exports.
Our evaluations of regions for animal
health closely consider a broad range of
factors widely accepted by the
international community for assessing
the disease risks associated with a
region. As discussed above, we provide
an opportunity for the public to view
and comment on our evaluations and
the information upon which they are
based prior to making a final
determination. Finding that a region is
free of a disease based on such an
evaluation does not guarantee, however,
that the region will always remain free
of that disease. Our evaluations enable
us to determine whether a disease is
present in a region at a given time,
ensure that the region has safeguards in
place to protect against introduction of
the disease, and ensure that the region
is capable of detecting and containing
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the disease should it be introduced
despite these measures.
Two commenters did not speak for or
against the specific changes, but raised
other issues, as follows.
One expressed concern that the
reason for the changes was to expedite
the evaluations for animal health status.
The commenter stated that this should
not be done at the expense of preventing
foreign animal disease introductions
into the United States.
We agree and point out that we are
not changing the way we conduct
evaluations. Our goal is to expedite the
process of a region supplying us with
the necessary information to conduct an
evaluation.
One commenter expressed concern
that APHIS emphasizes geographic, or
zonal, freedom from disease over other
approaches to trade in animal products
that effectively mitigate disease risks.
He mentioned compartmentalization
and commodity-based trade as two
alternatives. As examples of the latter,
he cited the international standards for
trade in fresh beef from regions that
vaccinate for foot-and-mouth disease
and the international standards for trade
in milk and deboned beef from regions
where the risk of bovine spongiform
encephalopathy is neither negligible nor
controlled. He stated that eradication of
livestock diseases may not always be
realistic or feasible, especially in places
like Africa, where the means for
achieving zone freedom (fences, for
example) can conflict with wildlife
preservation efforts (e.g., ensuring
wildlife have space and freedom to
roam).
We are making no changes to the
proposed rule in response to this
comment. While this rulemaking
addresses factors we consider when
assessing the disease status of a
geographic area, APHIS’ regulations also
include commodity-based requirements
that allow for the importation of a
variety of products from regions not
considered free of diseases of concern.
These requirements are contained
largely in 9 CFR part 94. Inquiries
regarding these requirements or requests
for approval of new requirements may
be directed to the National Center for
Import and Export: Telephone (301)
851–3300 or email
AskNCIE.Products@aphis.usda.gov.
Additionally, several of the
commenters addressed specific
provisions of the proposal.
One commenter objected to the
proposal to allow APHIS to initiate an
evaluation of a foreign country’s disease
status in the absence of a request from
that foreign country, stating that
multinational meat packers might lobby
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APHIS to conduct such evaluations in
order to source meat and livestock.
We are making no changes to the
proposed rule in response to this
comment. If there is a U.S. market for
meat or livestock from a foreign region
but APHIS has not yet evaluated its
disease risk, the foreign government of
that region will likely request an
evaluation because of the value those
exports would have for the foreign
region. In any case, as stated in the
proposed rule, APHIS anticipates that
most evaluations will be done at the
request of a foreign country. There may
be instances, however, when it will be
beneficial for APHIS to initiate an
evaluation, and we reserve the right to
do so. Even in such cases, we could not
conduct the evaluation without the
cooperation of the foreign government,
which would need to supply
information and allow access for any
necessary site visits. As with any
evaluation, there would be opportunity
for the public to review and comment
on the evaluation and proposed disease
status.
One commenter objected to our
proposal to remove the statement in
§ 92.2(d) that supporting information
submitted with country requests will be
made available to the public prior to
initiation of rulemaking. The
commenter stated withholding such
information will severely limit APHIS’
transparency. Another commenter
expressed concern that this change
would reduce the amount of time that
supporting information regarding a
country’s disease status is available to
the public.
We are making no change in response
to these comments. The intent of this
statement was to assure the public that
they will have access to, and
opportunity to comment on, the
information upon which APHIS bases
its evaluation, as well as the evaluation
itself. As discussed in the proposed
rule, this has been our practice, and it
will continue to be our practice.
Moreover, there will be no change in
when we make the supporting
information available. We will continue
to make both the supporting information
and the evaluation available when we
announce our intention to recognize the
animal health status of a region and
open the public comment period. We
were concerned that the statement we
proposed to remove suggested that the
supporting information might be made
available sooner, perhaps at the time of
the initial submission of the request,
when the information may be
incomplete or inadequate. Additionally,
this is not the only information APHIS
relies upon to make its determination.
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In addition to information provided by
the requesting country, we also gather
information from literature, reports, and
site visits and consider all of this in
preparing our evaluation. We believe
that the public should consider all of
the information together, and that it
could be confusing or misleading to
release it in stages.
One commenter requested that, when
we make available to the public a list of
regions that have requested recognition
of their animal health status, we include
an indication of the animal species and
diseases under evaluation with respect
to each region. Another commenter
recommended that we encourage foreign
jurisdictions to specify the type of
animal or product they wish to export
and that we also make that information
available to the public when we have it.
We agree with the suggestions.
Paragraph § 92.2(d) in this final rule
provides that APHIS will list on its Web
site each region that has requested
APHIS recognition of its animal health
status, the disease(s) under evaluation,
and, if the information is available, the
animal(s) or product(s) the region
wishes to export.
One commenter said that while the
proposed changes would facilitate the
work of foreign governments in
submitting information, he remains
concerned about the length of time it
can take to complete assessments. The
commenter referenced provisions in
Annex C of the WTO–SPS Agreement
that recommend that Members publish
the standard processing period for
evaluation requests or communicate the
anticipated processing period to the
applicant upon request.
We are making no changes to the
proposed rule in response to this
comment. Because the time required for
each evaluation varies, estimates must
be made on a case-by-case basis, which
APHIS will communicate with the
applicant upon request, consistent with
Annex C.
One commenter asked what we mean
by the wording ‘‘safely granted’’ in
proposed § 92.2(e), which says: ‘‘If, after
review and evaluation of the
information submitted in accordance
with paragraph (b) or (c) of this section,
APHIS believes the request can be safely
granted, APHIS will indicate its intent
and make its evaluation available for
public comment through a document
published in the Federal Register.’’
We mean that APHIS has determined
that imports from the region would
present a low risk of introducing a
particular disease into the United States
and may be safely imported.
A few commenters also made
suggestions or raised issues not directly
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related to the changes we proposed,
including expanding APHIS’ oversight
of other animals, including rodents; data
sharing among regulatory agencies;
conducting post-mortem examinations
of a representative sample of imported
livestock to rule out ‘‘potential disease’’;
and the agreement between the
European Commission and the United
States on sanitary measures. Because
these matters are outside the scope of
this rulemaking, we are not addressing
them here.
Therefore, for the reasons given in the
proposed rule and in this document, we
are adopting the proposed rule as a final
rule, with the change discussed above.
Executive Order 12866 and Regulatory
Flexibility Act
This final rule has been determined to
be not significant for the purposes of
Executive Order 12866 and, therefore,
has not been reviewed by the Office of
Management and Budget.
In accordance with the Regulatory
Flexibility Act, we have analyzed the
potential economic effects of this action
on small entities. The analysis is
summarized below. Copies of the full
analysis are available on the
Regulations.gov Web site (see footnote 1
in this document for a link to
Regulations.gov) or by contacting the
person listed under FOR FURTHER
INFORMATION CONTACT.
The economic analysis identifies
importers and producers of animals and
animal products as the small entities
most likely to be affected by this action
and considers the reduction in time
between receipt of a request by APHIS
and initiation of an evaluation.
Based on the information presented in
the analysis, we expect that decreasing
the amount of time and APHIS
resources required to conduct such an
evaluation would not have a significant
economic effect on the entities affected.
Under these circumstances, the
Administrator of the Animal and Plant
Health Inspection Service has
determined that this action will not
have a significant economic impact on
a substantial number of small entities.
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Executive Order 12988
This final rule has been reviewed
under Executive Order 12988, Civil
Justice Reform. This rule: (1) Preempts
all State and local laws and regulations
that are inconsistent with this rule; (2)
has no retroactive effect; and (3) does
not require administrative proceedings
before parties may file suit in court
challenging this rule.
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Paperwork Reduction Act
This final rule contains no new
information collection or recordkeeping
requirements under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501
et seq.).
List of Subjects in 9 CFR Part 92
Animal diseases, Imports, Livestock,
Poultry and poultry products, Region,
Reporting and recordkeeping
requirements.
Accordingly, we are amending 9 CFR
part 92 as follows:
PART 92—IMPORTATION OF ANIMALS
AND ANIMAL PRODUCTS;
PROCEDURES FOR REQUESTING
RECOGNITION OF REGIONS
1. The authority citation for part 92
continues to read as follows:
■
Authority: 7 U.S.C. 1622 and 8301–8317;
21 U.S.C. 136 and 136a; 31 U.S.C. 9701; 7
CFR 2.22, 2.80, and 371.4.
2. In § 92.2, paragraphs (a) through (f)
are revised to read as follows:
■
§ 92.2 Application for recognition of the
animal health status of a region.
(a) The representative of the national
government(s) of any country or
countries who has the authority to make
such a request may request that APHIS
recognize the animal health status of a
region.1 Such requests must be made in
English and must be sent to the
Administrator, c/o National Center for
Import and Export, VS, APHIS, 4700
River Road Unit 38, Riverdale, MD
20737–1231. (Where possible, include a
copy of the request and accompanying
information in electronic format.)
(b) Requests for recognition of the
animal health status of a region, other
than requests submitted in accordance
with paragraph (c) of this section, must
include, in English, the following
information about the region. More
detailed information regarding the
specific types of information that will
enable APHIS to most expeditiously
conduct an evaluation of the request is
available at https://www.aphis.usda.gov/
import_export/animals/
reg_request.shtml or by contacting the
Director, Sanitary Trade Issues Team,
National Center for Import and Export,
VS, APHIS, 4700 River Road Unit 38,
Riverdale, MD 20737.
(1) Scope of the evaluation being
requested.
(2) Veterinary control and oversight.
1 Additionally, APHIS may choose to initiate an
evaluation of the animal health status of a foreign
region on its own initiative. In such cases, APHIS
will follow the same evaluation and notification
procedures set forth in this section.
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44109
(3) Disease history and vaccination
practices.
(4) Livestock demographics and
traceability.
(5) Epidemiological separation from
potential sources of infection.
(6) Surveillance.
(7) Diagnostic laboratory capabilities.
(8) Emergency preparedness and
response.
(c) Requests for recognition that a
region is historically free of a disease
based on the amount of time that has
elapsed since the disease last occurred
in a region, if it has ever occurred, must
include, in English, the following
information about the region. More
detailed information regarding the
specific types of information that will
enable APHIS to most expeditiously
conduct an evaluation of the request is
available at https://www.aphis.usda.gov/
import_export/animals/
reg_request.shtml or by contacting the
Director, Sanitary Trade Issues Team,
National Center for Import and Export,
VS, APHIS, 4700 River Road Unit 38,
Riverdale, MD 20737. For a region to be
considered historically free of a disease,
the disease must not have been reported
in domestic livestock for at least the
past 25 years and must not have been
reported in wildlife for at least the past
10 years.
(1) Scope of the evaluation being
requested.
(2) Veterinary control and oversight.
(3) Disease history and vaccination
practices
(4) Disease notification.
(5) Disease detection.
(6) Barriers to disease introduction.
(d) A list of those regions that have
requested APHIS’ recognition of their
animal health status, the disease(s)
under evaluation, and, if available, the
animal(s) or product(s) the region
wishes to export, is available at https://
www.aphis.usda.gov/import_export/
animals/reg_request.shtml.
(e) If, after review and evaluation of
the information submitted in
accordance with paragraph (b) or (c) of
this section, APHIS believes the request
can be safely granted, APHIS will
indicate its intent and make its
evaluation available for public comment
through a document published in the
Federal Register.
(f) APHIS will provide a period of
time during which the public may
comment on its evaluation. During the
comment period, the public will have
access to the information upon which
APHIS based its evaluation, as well as
the evaluation itself. Once APHIS has
reviewed all comments received, it will
make a final determination regarding
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Federal Register / Vol. 77, No. 145 / Friday, July 27, 2012 / Rules and Regulations
the request and will publish that
determination in the Federal Register.
*
*
*
*
*
Done in Washington, DC, this 23rd day of
July 2012.
Kevin Shea,
Acting Administrator, Animal and Plant
Health Inspection Service.
[FR Doc. 2012–18324 Filed 7–26–12; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 29
[Docket No. FAA–2012–0785; Special
Conditions No. 29–027–SC]
Special Conditions: Agusta S.p.A.
Model AW139 and AB139 Helicopter,
Installation of a Search and Rescue
(SAR) Automatic Flight Control System
(AFCS)
Federal Aviation
Administration (FAA), DOT.
ACTION: Final special conditions; request
for comments.
AGENCY:
These special conditions are
issued for the Agusta S.p.A. (Agusta)
Model AW139 and AB139 helicopters.
These model helicopters, as modified by
Agusta, will have novel or unusual
design features associated with
installing an optional SAR AFCS. The
applicable airworthiness standards do
not contain adequate or appropriate
safety standards for this design feature.
These special conditions contain the
additional safety standards the
Administrator considers necessary to
show a level of safety equivalent to that
established by the existing
airworthiness standards.
DATES: The effective date of these
special conditions is July 18, 2012. We
must receive your comments by
September 25, 2012.
ADDRESSES: Send comments identified
by docket number [FAA–2012–0785]
using any of the following methods:
• Federal eRegulations Portal: Go to
https://www.regulations.gov and follow
the online instructions for sending your
comments electronically.
• Mail: Send comments to Docket
Operations, M–30, U.S. Department of
Transportation (DOT), 1200 New Jersey
Avenue SE., Room W12–140, West
Building Ground Floor, Washington, DC
20590–0001.
• Hand Delivery of Courier: Deliver
comments to the ‘‘Mail’’ address
between 9 a.m., and 5 p.m., Monday
through Friday, except Federal holidays.
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SUMMARY:
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• Fax: Fax comments to Docket
Operations at 202–493–2251.
Privacy: The FAA will post all
comments it receives, without change,
to https://regulations.gov, including any
personal information the commenter
provides. Using the search function of
the docket Web site, anyone can find
and read the electronic form of all
comments received into any FAA
docket, including the name of the
individual sending the comment (or
signing the comment for an association,
business, labor union, etc.). DOT’s
complete Privacy Act Statement can be
found in the Federal Register published
on April 11, 2000 (65 FR 19477–19478),
as well as at https://DocketsInfo.dot.gov.
Docket: You can read the background
documents or comments received at
https://www.regulations.gov. Follow the
online instructions for accessing the
docket or go to the Docket Operations in
Room @12–140 of the West Building
Ground Floor at 1200 New Jersey
Avenue SE., Washington, DC, between
9 a.m., and 5 p.m., Monday through
Friday, except Federal holidays.
FOR FURTHER INFORMATION CONTACT:
FAA, Aircraft Certification Service,
Rotorcraft Directorate, Regulations and
Policy Group (ASW–111), Attn: Stephen
Barbini, 2601 Meacham Blvd., Fort
Worth, Texas 76137; telephone (817)
222–5196; facsimile (817) 222–5961.
SUPPLEMENTARY INFORMATION:
Reason for No Prior Notice and
Comment Before Adoption
The substance of these special
conditions has been subjected to the
notice and comment period previously
and has been derived without
substantive change from those
previously issued. It is unlikely that
prior public comment would result in a
significant change from the substance
contained herein. Further, a delay in the
effective date of these special conditions
would significantly delay issuance of
the design approval and thus delivery of
the helicopter, which is imminent.
Therefore, the FAA has determined that
prior public notice and comment are
unnecessary, impracticable, and
contrary to the public interest, and finds
good cause exists for adopting these
special conditions upon issuance. The
FAA is requesting comments to allow
interested persons to submit views that
may not have been submitted in
response to the prior opportunities for
comment.
Comments Invited
While we did not precede this with a
notice of proposed special conditions,
we invite interested people to take part
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in this action by sending written
comments, data, or views. The most
helpful comments reference a specific
portion of the special conditions,
explain the reason for any
recommended change, and include
supporting data.
We will consider all comments we
receive by the closing date for
comments. We will consider comments
filed late if it is possible to do so
without incurring additional expense or
delay. We may change these special
conditions based on the comments we
receive.
Background and Discussion
On November 11, 2008, Agusta
applied for a change to Type Certificate
(TC) No. R00002RD to install an
optional SAR AFCS in the Model AB139
and AW139 helicopters. The AB139 and
AW139 models are transport category
helicopters certificated to Category A
and Category B requirements, and
instrument flight certificated under the
requirements of Appendix B to 14 CFR
part 29, Amendment 29–40.
There is a need to use dedicated
AFCS upper modes, in which a fully
coupled autopilot provides operational
SAR profiles, for SAR operations
conducted over water in offshore areas
clear of obstructions. The SAR modes
enable the helicopter pilot to fly fully
coupled maneuvers, to include
predefined search patterns during cruise
flight, and to transition from cruise
flight to a stabilized hover and
departure (transition from hover to
cruise flight). The SAR AFCS also
includes an auxiliary crew control that
allows another crewmember (such as a
hoist operator) to have limited authority
to control the helicopter’s longitudinal
and lateral position during hover
operations.
Flight operations conducted over
water at night may have an extremely
limited visual horizon with little visual
reference to the surface even when
conducted under Visual Meteorological
Conditions. Consequently, the
certification requirements for SAR
modes must meet Appendix B to 14 CFR
part 29 for helicopter instrument flight.
While this appendix prescribes
airworthiness criteria for instrument
flight, it does not consider operations
below instrument flight minimum speed
(VMINI), whereas the SAR modes allow
for coupled operations at low speed, allazimuth flight to zero airspeed (hover).
Since SAR operations have
traditionally been a public use mission,
the use of SAR modes in civil
operations requires special
airworthiness standards (special
conditions) to maintain a level of safety
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Agencies
[Federal Register Volume 77, Number 145 (Friday, July 27, 2012)]
[Rules and Regulations]
[Pages 44107-44110]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-18324]
========================================================================
Rules and Regulations
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains regulatory documents
having general applicability and legal effect, most of which are keyed
to and codified in the Code of Federal Regulations, which is published
under 50 titles pursuant to 44 U.S.C. 1510.
The Code of Federal Regulations is sold by the Superintendent of Documents.
Prices of new books are listed in the first FEDERAL REGISTER issue of each
week.
========================================================================
Federal Register / Vol. 77, No. 145 / Friday, July 27, 2012 / Rules
and Regulations
[[Page 44107]]
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
9 CFR Part 92
[Docket No. APHIS-2007-0158]
RIN 0579-AD30
Information From Foreign Regions Applying for Recognition of
Animal Health Status
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We are amending the regulations that govern the importation of
animals and animal products by consolidating the list of factors APHIS
considers when evaluating the animal health status of a foreign region
and by setting out new factors APHIS will consider when evaluating a
region as historically free of a specific disease. These changes will
make clearer the types of information APHIS needs from a requesting
region in order to conduct an evaluation.
DATES: Effective Date: August 27, 2012.
FOR FURTHER INFORMATION CONTACT: Dr. Kelly Rhodes, Regionalization
Evaluation Services, Sanitary Trade Issues Team, National Center for
Import and Export, VS, APHIS, 4700 River Road Unit 38, Riverdale, MD
20737-1231; (301) 851-3300.
SUPPLEMENTARY INFORMATION:
Background
The regulations in 9 CFR part 92, ``Importation of Animals and
Animal Products; Procedures for Requesting Recognition of Regions''
(referred to below as the regulations), set forth the process by which
a foreign government may request recognition of the animal health
status of a region.
Section 92.2 of the regulations requires that such requests be
accompanied by information regarding the region that will enable the
Animal and Plant Health Inspection Service (APHIS) of the U.S.
Department of Agriculture to evaluate the request.
On December 28, 2011, we published in the Federal Register (76 FR
81404-81408, Docket No. APHIS-2007-0158) a proposal \1\ to amend the
regulations by consolidating the 11 factors listed in Sec. 92.2(b)
that APHIS considers when evaluating the animal health status of a
foreign region into 8 factors. We also proposed to establish criteria
for recognizing a region as historically free of a specific disease.
Our intent was to make clearer the types of information APHIS needs
from a requesting region to conduct an evaluation. Additionally,
although our regulations focus on requests from foreign regions, we
noted that APHIS could initiate an evaluation of the disease status of
a foreign region and, if we did, would conduct the evaluation using
these same factors. We also proposed to remove a statement in Sec.
92.2(d) that supporting information submitted with country requests
will be made available to the public prior to initiation of rulemaking.
We proposed to replace it with a statement that a list of regions that
have requested recognition of their animal health status will be
available to the public, and to leave in place a statement in Sec.
92.2(f) that when APHIS makes its evaluation available for public
comment, the public will have access to the information upon which
APHIS based its evaluation, as well as the evaluation itself.
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\1\ To view the proposed rule and the comments we received, go
to https://www.regulations.gov/#!docketDetail;D=APHIS-2007-0158.
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We solicited comments concerning our proposal for 60 days ending
February 27, 2012. We received 12 comments (including two from the same
person) by that date. They were from an organization representing pork
producers, an organization representing cattle farmers and ranchers, an
organization representing U.S. consumers, a wildlife conservation
society, a State board of animal health, foreign governments, and
individuals.
Six commenters supported the proposed changes.
Three commenters objected to the proposed rule. Two of the three
said that they oppose the concept of regionalization for animal health
status. Two also said they were concerned about APHIS' ability to
predict outbreaks or detect disease threats under the current 11
factors and oppose finalizing a rule predicated on those factors. They
cited several instances where regions APHIS had recognized as free of a
disease had subsequently experienced an outbreak of that disease. One
commenter also said that APHIS should not adopt international criteria
for evaluating a region as historically free of a disease until we have
conducted a scientific study to determine whether such recommendations
are, in fact, capable of adequately assessing whether a country is
historically free of a disease.
We are making no changes to the proposed rule in response to these
comments. Regionalization is an important principle of the World Trade
Organization Agreement on the Application of Sanitary and Phytosanitary
Measures (WTO-SPS Agreement). Regionalization is based on recognition
that pest and disease conditions may vary across a country as a result
of ecological, environmental, and epidemiological factors, and on the
premise that these differences should be taken into account in
developing science-based regulatory measures. The United States has
successfully applied the concept for decades in domestic disease
control and eradication programs, and regionalization of the United
States for bluetongue and other diseases has facilitated exports.
Our evaluations of regions for animal health closely consider a
broad range of factors widely accepted by the international community
for assessing the disease risks associated with a region. As discussed
above, we provide an opportunity for the public to view and comment on
our evaluations and the information upon which they are based prior to
making a final determination. Finding that a region is free of a
disease based on such an evaluation does not guarantee, however, that
the region will always remain free of that disease. Our evaluations
enable us to determine whether a disease is present in a region at a
given time, ensure that the region has safeguards in place to protect
against introduction of the disease, and ensure that the region is
capable of detecting and containing
[[Page 44108]]
the disease should it be introduced despite these measures.
Two commenters did not speak for or against the specific changes,
but raised other issues, as follows.
One expressed concern that the reason for the changes was to
expedite the evaluations for animal health status. The commenter stated
that this should not be done at the expense of preventing foreign
animal disease introductions into the United States.
We agree and point out that we are not changing the way we conduct
evaluations. Our goal is to expedite the process of a region supplying
us with the necessary information to conduct an evaluation.
One commenter expressed concern that APHIS emphasizes geographic,
or zonal, freedom from disease over other approaches to trade in animal
products that effectively mitigate disease risks. He mentioned
compartmentalization and commodity-based trade as two alternatives. As
examples of the latter, he cited the international standards for trade
in fresh beef from regions that vaccinate for foot-and-mouth disease
and the international standards for trade in milk and deboned beef from
regions where the risk of bovine spongiform encephalopathy is neither
negligible nor controlled. He stated that eradication of livestock
diseases may not always be realistic or feasible, especially in places
like Africa, where the means for achieving zone freedom (fences, for
example) can conflict with wildlife preservation efforts (e.g.,
ensuring wildlife have space and freedom to roam).
We are making no changes to the proposed rule in response to this
comment. While this rulemaking addresses factors we consider when
assessing the disease status of a geographic area, APHIS' regulations
also include commodity-based requirements that allow for the
importation of a variety of products from regions not considered free
of diseases of concern. These requirements are contained largely in 9
CFR part 94. Inquiries regarding these requirements or requests for
approval of new requirements may be directed to the National Center for
Import and Export: Telephone (301) 851-3300 or email
AskNCIE.Products@aphis.usda.gov.
Additionally, several of the commenters addressed specific
provisions of the proposal.
One commenter objected to the proposal to allow APHIS to initiate
an evaluation of a foreign country's disease status in the absence of a
request from that foreign country, stating that multinational meat
packers might lobby APHIS to conduct such evaluations in order to
source meat and livestock.
We are making no changes to the proposed rule in response to this
comment. If there is a U.S. market for meat or livestock from a foreign
region but APHIS has not yet evaluated its disease risk, the foreign
government of that region will likely request an evaluation because of
the value those exports would have for the foreign region. In any case,
as stated in the proposed rule, APHIS anticipates that most evaluations
will be done at the request of a foreign country. There may be
instances, however, when it will be beneficial for APHIS to initiate an
evaluation, and we reserve the right to do so. Even in such cases, we
could not conduct the evaluation without the cooperation of the foreign
government, which would need to supply information and allow access for
any necessary site visits. As with any evaluation, there would be
opportunity for the public to review and comment on the evaluation and
proposed disease status.
One commenter objected to our proposal to remove the statement in
Sec. 92.2(d) that supporting information submitted with country
requests will be made available to the public prior to initiation of
rulemaking. The commenter stated withholding such information will
severely limit APHIS' transparency. Another commenter expressed concern
that this change would reduce the amount of time that supporting
information regarding a country's disease status is available to the
public.
We are making no change in response to these comments. The intent
of this statement was to assure the public that they will have access
to, and opportunity to comment on, the information upon which APHIS
bases its evaluation, as well as the evaluation itself. As discussed in
the proposed rule, this has been our practice, and it will continue to
be our practice. Moreover, there will be no change in when we make the
supporting information available. We will continue to make both the
supporting information and the evaluation available when we announce
our intention to recognize the animal health status of a region and
open the public comment period. We were concerned that the statement we
proposed to remove suggested that the supporting information might be
made available sooner, perhaps at the time of the initial submission of
the request, when the information may be incomplete or inadequate.
Additionally, this is not the only information APHIS relies upon to
make its determination. In addition to information provided by the
requesting country, we also gather information from literature,
reports, and site visits and consider all of this in preparing our
evaluation. We believe that the public should consider all of the
information together, and that it could be confusing or misleading to
release it in stages.
One commenter requested that, when we make available to the public
a list of regions that have requested recognition of their animal
health status, we include an indication of the animal species and
diseases under evaluation with respect to each region. Another
commenter recommended that we encourage foreign jurisdictions to
specify the type of animal or product they wish to export and that we
also make that information available to the public when we have it.
We agree with the suggestions. Paragraph Sec. 92.2(d) in this
final rule provides that APHIS will list on its Web site each region
that has requested APHIS recognition of its animal health status, the
disease(s) under evaluation, and, if the information is available, the
animal(s) or product(s) the region wishes to export.
One commenter said that while the proposed changes would facilitate
the work of foreign governments in submitting information, he remains
concerned about the length of time it can take to complete assessments.
The commenter referenced provisions in Annex C of the WTO-SPS Agreement
that recommend that Members publish the standard processing period for
evaluation requests or communicate the anticipated processing period to
the applicant upon request.
We are making no changes to the proposed rule in response to this
comment. Because the time required for each evaluation varies,
estimates must be made on a case-by-case basis, which APHIS will
communicate with the applicant upon request, consistent with Annex C.
One commenter asked what we mean by the wording ``safely granted''
in proposed Sec. 92.2(e), which says: ``If, after review and
evaluation of the information submitted in accordance with paragraph
(b) or (c) of this section, APHIS believes the request can be safely
granted, APHIS will indicate its intent and make its evaluation
available for public comment through a document published in the
Federal Register.''
We mean that APHIS has determined that imports from the region
would present a low risk of introducing a particular disease into the
United States and may be safely imported.
A few commenters also made suggestions or raised issues not
directly
[[Page 44109]]
related to the changes we proposed, including expanding APHIS'
oversight of other animals, including rodents; data sharing among
regulatory agencies; conducting post-mortem examinations of a
representative sample of imported livestock to rule out ``potential
disease''; and the agreement between the European Commission and the
United States on sanitary measures. Because these matters are outside
the scope of this rulemaking, we are not addressing them here.
Therefore, for the reasons given in the proposed rule and in this
document, we are adopting the proposed rule as a final rule, with the
change discussed above.
Executive Order 12866 and Regulatory Flexibility Act
This final rule has been determined to be not significant for the
purposes of Executive Order 12866 and, therefore, has not been reviewed
by the Office of Management and Budget.
In accordance with the Regulatory Flexibility Act, we have analyzed
the potential economic effects of this action on small entities. The
analysis is summarized below. Copies of the full analysis are available
on the Regulations.gov Web site (see footnote 1 in this document for a
link to Regulations.gov) or by contacting the person listed under FOR
FURTHER INFORMATION CONTACT.
The economic analysis identifies importers and producers of animals
and animal products as the small entities most likely to be affected by
this action and considers the reduction in time between receipt of a
request by APHIS and initiation of an evaluation.
Based on the information presented in the analysis, we expect that
decreasing the amount of time and APHIS resources required to conduct
such an evaluation would not have a significant economic effect on the
entities affected.
Under these circumstances, the Administrator of the Animal and
Plant Health Inspection Service has determined that this action will
not have a significant economic impact on a substantial number of small
entities.
Executive Order 12988
This final rule has been reviewed under Executive Order 12988,
Civil Justice Reform. This rule: (1) Preempts all State and local laws
and regulations that are inconsistent with this rule; (2) has no
retroactive effect; and (3) does not require administrative proceedings
before parties may file suit in court challenging this rule.
Paperwork Reduction Act
This final rule contains no new information collection or
recordkeeping requirements under the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.).
List of Subjects in 9 CFR Part 92
Animal diseases, Imports, Livestock, Poultry and poultry products,
Region, Reporting and recordkeeping requirements.
Accordingly, we are amending 9 CFR part 92 as follows:
PART 92--IMPORTATION OF ANIMALS AND ANIMAL PRODUCTS; PROCEDURES FOR
REQUESTING RECOGNITION OF REGIONS
0
1. The authority citation for part 92 continues to read as follows:
Authority: 7 U.S.C. 1622 and 8301-8317; 21 U.S.C. 136 and 136a;
31 U.S.C. 9701; 7 CFR 2.22, 2.80, and 371.4.
0
2. In Sec. 92.2, paragraphs (a) through (f) are revised to read as
follows:
Sec. 92.2 Application for recognition of the animal health status of
a region.
(a) The representative of the national government(s) of any country
or countries who has the authority to make such a request may request
that APHIS recognize the animal health status of a region.\1\ Such
requests must be made in English and must be sent to the Administrator,
c/o National Center for Import and Export, VS, APHIS, 4700 River Road
Unit 38, Riverdale, MD 20737-1231. (Where possible, include a copy of
the request and accompanying information in electronic format.)
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\1\ Additionally, APHIS may choose to initiate an evaluation of
the animal health status of a foreign region on its own initiative.
In such cases, APHIS will follow the same evaluation and
notification procedures set forth in this section.
---------------------------------------------------------------------------
(b) Requests for recognition of the animal health status of a
region, other than requests submitted in accordance with paragraph (c)
of this section, must include, in English, the following information
about the region. More detailed information regarding the specific
types of information that will enable APHIS to most expeditiously
conduct an evaluation of the request is available at https://www.aphis.usda.gov/import_export/animals/reg_request.shtml or by
contacting the Director, Sanitary Trade Issues Team, National Center
for Import and Export, VS, APHIS, 4700 River Road Unit 38, Riverdale,
MD 20737.
(1) Scope of the evaluation being requested.
(2) Veterinary control and oversight.
(3) Disease history and vaccination practices.
(4) Livestock demographics and traceability.
(5) Epidemiological separation from potential sources of infection.
(6) Surveillance.
(7) Diagnostic laboratory capabilities.
(8) Emergency preparedness and response.
(c) Requests for recognition that a region is historically free of
a disease based on the amount of time that has elapsed since the
disease last occurred in a region, if it has ever occurred, must
include, in English, the following information about the region. More
detailed information regarding the specific types of information that
will enable APHIS to most expeditiously conduct an evaluation of the
request is available at https://www.aphis.usda.gov/import_export/animals/reg_request.shtml or by contacting the Director, Sanitary
Trade Issues Team, National Center for Import and Export, VS, APHIS,
4700 River Road Unit 38, Riverdale, MD 20737. For a region to be
considered historically free of a disease, the disease must not have
been reported in domestic livestock for at least the past 25 years and
must not have been reported in wildlife for at least the past 10 years.
(1) Scope of the evaluation being requested.
(2) Veterinary control and oversight.
(3) Disease history and vaccination practices
(4) Disease notification.
(5) Disease detection.
(6) Barriers to disease introduction.
(d) A list of those regions that have requested APHIS' recognition
of their animal health status, the disease(s) under evaluation, and, if
available, the animal(s) or product(s) the region wishes to export, is
available at https://www.aphis.usda.gov/import_export/animals/reg_request.shtml.
(e) If, after review and evaluation of the information submitted in
accordance with paragraph (b) or (c) of this section, APHIS believes
the request can be safely granted, APHIS will indicate its intent and
make its evaluation available for public comment through a document
published in the Federal Register.
(f) APHIS will provide a period of time during which the public may
comment on its evaluation. During the comment period, the public will
have access to the information upon which APHIS based its evaluation,
as well as the evaluation itself. Once APHIS has reviewed all comments
received, it will make a final determination regarding
[[Page 44110]]
the request and will publish that determination in the Federal
Register.
* * * * *
Done in Washington, DC, this 23rd day of July 2012.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2012-18324 Filed 7-26-12; 8:45 am]
BILLING CODE 3410-34-P