Introductions of Plants Genetically Engineered To Produce Industrial Compounds, 23009-23011 [05-8860]
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23009
Rules and Regulations
Federal Register
Vol. 70, No. 85
Wednesday, May 4, 2005
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
7 CFR Part 340
[Docket No. 03–038–2]
RIN 0579–AB89
Introductions of Plants Genetically
Engineered To Produce Industrial
Compounds
Animal and Plant Health
Inspection Service, USDA.
ACTION: Affirmation of interim rule as
final rule.
AGENCY:
SUMMARY: We are adopting as a final
rule, without change, an interim rule
that amended our regulations regarding
genetically engineered organisms to
require that introductions of plants
genetically engineered to encode
compounds for industrial use be
conducted only under permit. Prior to
the interim rule, such introductions
could be accomplished under
notification, an expedited permitting
procedure. The interim rule was
necessary to strengthen our regulations
for introductions of this small subgroup
of genetically engineered plants until
such time as the issues related to these
plants are fully considered in
conjunction with subsequent regulatory
revision.
DATES: The interim rule became
effective on August 6, 2003.
FOR FURTHER INFORMATION CONTACT: Dr.
John Turner, Director, Policy Division,
BRS, APHIS, 4700 River Road Unit 146,
Riverdale, MD 20737–1238; (301) 734–
8365.
SUPPLEMENTARY INFORMATION:
Background
The regulations in 7 CFR part 340,
‘‘Introduction of Organisms and
Products Altered or Produced Through
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13:01 May 03, 2005
Jkt 205001
Genetic Engineering Which are Plant
Pests or Which There is Reason to
Believe are Plant Pests’’ (referred to
below as the regulations), govern the
introduction (importation, interstate
movement, or release into the
environment) of any organism or
product altered or produced through
genetic engineering that is a plant pest
or that there is reason to believe is a
plant pest, or any product which
contains such an organism that is
unclassified and/or whose classification
is unknown. The regulations refer to
such organisms as ‘‘regulated articles.’’
With certain limited exceptions, the
introduction of any regulated article is
prohibited unless that introduction is
authorized by a permit or, for specific
classes of regulated articles, the
Administrator of the Animal and Plant
Health Inspection Service (APHIS) has
been notified of the introduction in
accordance with § 340.3 of the
regulations, which provides for the use,
under certain circumstances, of an
expedited permitting procedure called
notification.
The notification option was added to
the regulations in 1993 (58 FR 17044–
53043, Docket No. 92–156–02) in order
to expedite introductions for certain
types of low risk plants with which
APHIS had considerable regulatory
experience. Under the notification
procedure, the regulated article to be
introduced must be a plant, and the
types of genetic modifications to the
plant must meet the eligibility criteria
described in § 340.3(b). Development of
those criteria was based upon the types
of genetic modifications that APHIS had
reviewed and evaluated many times
over the preceding years of issuing
permits.
At the time the regulations were
amended to provide for the use of
notification, the types of genetically
engineered plants that had industrial
uses were typically those in which
nutritional components, such as oil
content, were being engineered. Since
APHIS had significant regulatory
experience with the types of traits then
being introduced into these plants,
industrial plants were eligible for the
notification option. In contrast, the
notification regulations in
§ 340.3(b)(4)(iii) prohibited the use of
notification for introductions of plants
genetically engineered to encode
compounds for pharmaceutical use,
PO 00000
Frm 00001
Fmt 4700
Sfmt 4700
thus continuing to require a permit for
such introductions, because of our lack
of regulatory experience and scientific
familiarity with these types of
introduced traits.
In 2003, we noted that a number of
more recent introductions of plants
engineered to produce compounds
intended for industrial use had been for
traits different than what we were
seeing in 1993. Those more recent
introductions were for non-food, nonfeed traits with which APHIS has little
regulatory experience or scientific
familiarity. Based on the expansion of
the technology and the new non-food,
non-feed uses of industrial plants being
developed, we believed it to be prudent
and necessary to remove the notification
option for all industrials pending the
completion of our ongoing review of
part 340.
Therefore, in an interim rule effective
and published in the Federal Register
on August 6, 2003 (68 FR 46434–46436,
Docket No. 03–038–1), we amended the
regulations to require that introductions
of plants genetically engineered to
encode compounds for industrial use be
conducted only under permit. For
purposes of the interim rule, plants
engineered to produce industrial
compounds include those plants that
meet the following three criteria: (1) The
plants are engineered to produce
compounds that are new to the plant; (2)
the new compound has not been
commonly used in food or feed; and (3)
the new compound is being expressed
for non-food, non-feed industrial uses.
Industrial uses include, but are not
limited to, detergent manufacturing,
paper production, and mineral recovery.
Comments on the interim rule were
required to be received on or before
October 6, 2003. We received 12
comments by that date. The comments
were from companies and organizations
involved in biotechnology, an organic
certification service, a university
biologist, a private citizen, an
association of crop production and
protection companies, and associations
representing food producers, processors,
and manufacturers. One of the
commenters voiced opposition to
genetically modified plants generally,
but offered no specific comments
relating to the interim rule. The
remaining commenters expressed their
support for the interim rule, although
several made specific suggestions or
E:\FR\FM\04MYR1.SGM
04MYR1
23010
Federal Register / Vol. 70, No. 85 / Wednesday, May 4, 2005 / Rules and Regulations
raised related issues. Those comments
are discussed below.
Several commenters raised issues
related to the potential for plants
engineered to produce industrial
compounds to contaminate or adulterate
food crops. Some commenters urged
APHIS to require that the introduction
of such crops be conducted under
conditions of 100 percent containment
(e.g., in secure greenhouses) or
geographic isolation to ensure that
adulteration does not occur. Other
commenters stated that APHIS should
not allow food crops to be genetically
modified to produce industrial
compounds in order to eliminate the
potential for the spread of transgenic
pollen to sexually compatible nonmodified plants. One of these
commenters further suggested that if
food crops are to be used to produce
industrial compounds, self-pollinating
crops should be used to the maximum
extent possible.
APHIS wishes to reiterate that the
purpose of the interim rule was to
ensure that introductions of plants
engineered to produce industrial
compounds will be conducted under
permit rather than under notification.
Although there are administrative
differences between these procedures,
the goal of each is to ensure that plants
are confined during movement and field
testing and do not persist in the
environment, and both are designed to
achieve high levels of safety. In
addition, use of any regulated article
originating from a field test as food or
feed would be subject to the regulatory
authority of the Food and Drug
Administration (FDA). Failure to meet
any of the requirements associated with
APHIS permits and notifications can
lead to substantial fines, as provided in
the Plant Protection Act.
One commenter agreed with the three
criteria set out in the interim rule to
describe plants engineered to produce
industrial compounds, but suggested
that food or feed plants genetically
engineered to produce dietary
supplements that are acceptable only in
dietary supplements should also be
considered industrial plants and thus
ineligible for introduction using the
notification option.
Plants, whether genetically
engineered or not, yield a variety of
compounds that are used to produce
dietary supplements. If a food or feed
plant naturally produces a compound
used in dietary supplements, and that
plant has been genetically engineered to
produce more of that compound, then
that plant would not be considered an
industrial plant (and thus would be
eligible for introduction using
VerDate jul<14>2003
13:01 May 03, 2005
Jkt 205001
notification) because the first of the
three criteria is that ‘‘the plants are
engineered to produce compounds that
are new to the plant.’’ However, if the
compound is new to the plant, has not
been commonly used in food or feed,
and is being expressed for non-food,
non-feed industrial uses, then the plant
would be considered an industrial plant
under our criteria and thus eligible for
introduction only under permit.
Again with respect to the three
criteria, one commenter suggested that
APHIS may wish to clarify those criteria
regarding the circumstances under
which a permit will and will not be
required for field testing and to provide
examples of both to assist the public
and those developing industrial proteins
in better understanding those
circumstances.
APHIS may, when needed, provide
additional written guidance illustrating
the criteria that define whether a field
test qualifies for the notification
procedure or if it must be conducted
under permit. The agency has provided
such written guidance since the
implementation of the regulations in
part 340 in 1987, offering additional
examples that would not necessarily be
appropriate for inclusion in the
regulations themselves and updating or
clarifying that guidance as necessary.
When the notification option was added
to the regulations in 1993, APHIS
published a user’s guide to notifications.
Copies of our user’s guides are available
in print form and may be viewed on the
Agency Web site at https://
www.aphis.usda.gov/brs.
One commenter stated that, while it
may be currently necessary to require
that introductions of industrial plants be
conducted only under permit, over time
APHIS should gain sufficient familiarity
with certain industrial compounds to
allow plants producing such
compounds to be grown under
notification procedures. The commenter
urged APHIS to adopt this approach as
it considers amending its regulations in
7 CFR part 340.
APHIS continually evaluates its
regulations in the light of increased
experience and familiarity with
scientific, technical, and administrative
considerations. In this or any other
situation, the accumulation of
experience or the availability of
additional information may lead us to
initiate rulemaking to update the
regulations.
Another commenter, also with an eye
toward future amendments to the
regulations, suggested that APHIS
provide for enhanced oversight for
industrial plants in the areas of
confinement controls, site security, and
PO 00000
Frm 00002
Fmt 4700
Sfmt 4700
compliance verification and the use of
third-party auditors, standard-setting
organizations, and standard operating
procedures as a quality control
mechanism.
APHIS agrees that it is appropriate to
take the considerations identified by the
commenter into account as we continue
to review our existing regulations in
part 340 and develop potential
amendments to those regulations.
Continuing Effect of Amendment
The preamble of the interim rule
stated that our amendment to the
regulations in part 340 to remove the
notification options for plants
genetically engineered to encode
compounds for industrial use would be
in effect until December 31, 2004. At the
time we made that statement, and as we
explained in the interim rule, it was our
intent to remove the notification option
for all industrials pending the
completion of our ongoing review of
part 340. That review, which is not yet
complete, is being conducted as part of
our consideration of possible
amendments to the regulations to,
among other things, include genetically
engineered organisms that may pose a
noxious weed risk and genetically
engineered biological control agents.
On January 23, 2004, we published a
notice in the Federal Register (69 FR
3271–3272, Docket No. 03–031–2), in
which we advised the public that we
intend to prepare an environmental
impact statement (EIS) in connection
with potential changes to the
regulations regarding the importation,
interstate movement, and environmental
release of certain genetically engineered
organisms. The notice identified
potential issues and alternatives that
will be studied in the EIS and requested
public comment to further delineate the
scope of the issues and alternatives.
We believe that it is essential that we
consider the findings of the EIS as part
of our review of the existing regulations
in part 340, but the EIS is not yet at a
stage at which we may do so. Therefore,
consistent with our stated intent to
remove the notification option for all
industrials pending the completion of
our review of part 340, we are
announcing that the current
requirement that introductions of plants
genetically engineered to encode
compounds for industrial use be
conducted only under permit will
continue in effect beyond December 31,
2004, until the completion of our review
of the regulations in part 340. We expect
that our review will include the
publication in the Federal Register of a
proposed rule for public comment and
E:\FR\FM\04MYR1.SGM
04MYR1
Federal Register / Vol. 70, No. 85 / Wednesday, May 4, 2005 / Rules and Regulations
the subsequent publication of a final
rule.
Therefore, for the reasons given in the
interim rule and in this document, we
are adopting the interim rule as a final
rule without change.
This action also affirms the
information contained in the interim
rule concerning Executive Order 12866
and the Regulatory Flexibility Act,
Executive Orders 12372 and 12988, and
the Paperwork Reduction Act.
Further, this action has been
determined to be significant for the
purposes of Executive Order 12866 and,
therefore, has been reviewed by the
Office of Management and Budget.
List of Subjects in 7 CFR Part 340
Administrative practice and
procedure, Biotechnology, Genetic
engineering, Imports, Packaging and
containers, Plant diseases and pests,
Transportation.
PART 340—INTRODUCTION OF
ORGANISMS AND PRODUCTS
ALTERED OR PRODUCED THROUGH
GENETIC ENGINEERING WHICH ARE
PLANT PESTS OR WHICH THERE IS
REASON TO BELIEVE ARE PLANT
PESTS
Accordingly, we are adopting as a final
rule, without change, the interim rule
that amended 7 CFR part 340 and that
was published at 68 FR 46434–46436 on
August 6, 2003.
I
Done in Washington, DC, this 28th day of
April 2005 .
Bill Hawks,
Under Secretary for Marketing and Regulatory
Programs.
[FR Doc. 05–8860 Filed 5–3–05; 8:45 am]
BILLING CODE 3410–34–P
NATIONAL INDIAN GAMING
COMMISSION
25 CFR Part 542
RIN 3141–AA27
Minimum Internal Control Standards
National Indian Gaming
Commission.
ACTION: Final rule.
AGENCY:
SUMMARY: In response to the inherent
risks of gaming enterprises and the
resulting need for effective internal
controls in Tribal gaming operations,
the National Indian Gaming
Commission (Commission or NIGC) first
developed Minimum Internal Control
Standards (MICS) for Indian gaming in
1999, and then later revised them in
2002. The Commission recognized from
VerDate jul<14>2003
13:01 May 03, 2005
Jkt 205001
the outset that periodic technical
adjustments and revisions would be
necessary in order to keep the MICS
effective in protecting Tribal gaming
assets and the interests of Tribal
stakeholders and the gaming public. To
that end, the following final rule
revisions contain certain corrections
and revisions to the Commission’s
existing MICS, which are necessary to
correct erroneous citations or references
in the MICS and to clarify, improve, and
update other existing MICS provisions.
The purpose of these final MICS
revisions is to address apparent
shortcomings in the MICS and various
changes in Tribal gaming technology
and methods. Public comment to these
final MICS revisions was received by
the Commission for a period of 48 days
after the date of their publication in the
Federal Register as a proposed rule on
December 1, 2004. Thereafter, the
comment period was extended for an
additional 31 days until February 18,
2005.
After consideration of all received
comments, the Commission has made
whatever changes to the proposed
revisions that it deemed appropriate and
is now promulgating and publishing the
final revisions to the Commission’s
MICS Rule, 25 CFR part 542.
DATES: Effective Date: May 4, 2005.
Compliance Date: On or before July 5,
2005, the Tribal gaming regulatory
authority shall: (1) In accordance with
the Tribal gaming ordinance, establish
and implement Tribal internal control
standards that shall provide a level of
control that equals or exceeds the
revised standards set forth herein; and
(2) establish a deadline no later than
September 1, 2005, by which a gaming
operation must come into compliance
with the Tribal internal control
standards. However, the Tribal gaming
regulatory authority may extend the
deadline by an additional 60 days if
written notice is provided to the
Commission no later than September 1,
2005. Such notification must cite the
specific revisions to which the
extension pertains.
FOR FURTHER INFORMATION CONTACT:
Vice-Chairman Nelson Westrin, (202)
632–7003 (not a toll-free number).
SUPPLEMENTARY INFORMATION:
Background
On January 5, 1999, the Commission
first published its Minimum Internal
Control Standards (MICS) as a Final
Rule. As gaming Tribes and the
Commission gained practical experience
applying the MICS, it became apparent
that some of the standards required
clarification or modification to operate
PO 00000
Frm 00003
Fmt 4700
Sfmt 4700
23011
as the Commission had intended and to
accommodate changes and advances
that had occurred over the years in
Tribal gaming technology and methods.
Consequently, the Commission, working
with an Advisory Committee composed
of Commission and Tribal
representatives, published the new final
revised MICS rule on June 27, 2002. As
the result of the practical experience of
the Commission and Tribes working
with the newly revised MICS, it has
once again become apparent that
additional corrections, clarifications,
and modifications are needed to ensure
that the MICS continue to operate as the
Commission intended. To identify
which of the current MICS need
correction, clarification or modification,
the Commission initially solicited input
and guidance from NIGC employees,
who have extensive gaming regulatory
expertise and experience and work
closely with Tribal gaming regulators in
monitoring the implementation,
operation, and effect of the MICS in
Tribal gaming operations. The resulting
input from NIGC staff convinced the
Commission that the MICS require
continuing review and prompt revision
on an ongoing basis to keep them
effective and up-to-date. To address this
need, the Commission decided to
establish a Standing MICS Advisory
Committee to assist it in both
identifying and developing necessary
MICS revisions and revisions on an
ongoing basis. In recognition of its
government-to-government relationship
with Tribes and related commitment to
meaningful Tribal consultation, the
Commission requested gaming Tribes,
in January 2004, for nominations of
Tribal representatives to serve on its
Standing MICS Advisory Committee.
From the 27 Tribal nominations that it
received, the Commission selected 9
Tribal representatives in March 2004 to
serve on the Committee. The
Commission’s Tribal Committee
member selections were based on
several factors, including the regulatory
experience and background of the
individuals nominated, the size(s) of
their affiliated Tribal gaming
operation(s), the types of games played
at their affiliated Tribal gaming
operation(s), and the areas of the
country in which their affiliated Tribal
gaming operation(s) are located. The
selection process was very difficult,
because numerous highly qualified
Tribal representatives were nominated
to serve on this important Committee.
As expected, the benefit of including
Tribal representatives on the
Committee, who work daily with the
MICS, has proved to be invaluable.
E:\FR\FM\04MYR1.SGM
04MYR1
Agencies
[Federal Register Volume 70, Number 85 (Wednesday, May 4, 2005)]
[Rules and Regulations]
[Pages 23009-23011]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-8860]
========================================================================
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. 70, No. 85 / Wednesday, May 4, 2005 / Rules
and Regulations
[[Page 23009]]
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
7 CFR Part 340
[Docket No. 03-038-2]
RIN 0579-AB89
Introductions of Plants Genetically Engineered To Produce
Industrial Compounds
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Affirmation of interim rule as final rule.
-----------------------------------------------------------------------
SUMMARY: We are adopting as a final rule, without change, an interim
rule that amended our regulations regarding genetically engineered
organisms to require that introductions of plants genetically
engineered to encode compounds for industrial use be conducted only
under permit. Prior to the interim rule, such introductions could be
accomplished under notification, an expedited permitting procedure. The
interim rule was necessary to strengthen our regulations for
introductions of this small subgroup of genetically engineered plants
until such time as the issues related to these plants are fully
considered in conjunction with subsequent regulatory revision.
DATES: The interim rule became effective on August 6, 2003.
FOR FURTHER INFORMATION CONTACT: Dr. John Turner, Director, Policy
Division, BRS, APHIS, 4700 River Road Unit 146, Riverdale, MD 20737-
1238; (301) 734-8365.
SUPPLEMENTARY INFORMATION:
Background
The regulations in 7 CFR part 340, ``Introduction of Organisms and
Products Altered or Produced Through Genetic Engineering Which are
Plant Pests or Which There is Reason to Believe are Plant Pests''
(referred to below as the regulations), govern the introduction
(importation, interstate movement, or release into the environment) of
any organism or product altered or produced through genetic engineering
that is a plant pest or that there is reason to believe is a plant
pest, or any product which contains such an organism that is
unclassified and/or whose classification is unknown. The regulations
refer to such organisms as ``regulated articles.''
With certain limited exceptions, the introduction of any regulated
article is prohibited unless that introduction is authorized by a
permit or, for specific classes of regulated articles, the
Administrator of the Animal and Plant Health Inspection Service (APHIS)
has been notified of the introduction in accordance with Sec. 340.3 of
the regulations, which provides for the use, under certain
circumstances, of an expedited permitting procedure called
notification.
The notification option was added to the regulations in 1993 (58 FR
17044-53043, Docket No. 92-156-02) in order to expedite introductions
for certain types of low risk plants with which APHIS had considerable
regulatory experience. Under the notification procedure, the regulated
article to be introduced must be a plant, and the types of genetic
modifications to the plant must meet the eligibility criteria described
in Sec. 340.3(b). Development of those criteria was based upon the
types of genetic modifications that APHIS had reviewed and evaluated
many times over the preceding years of issuing permits.
At the time the regulations were amended to provide for the use of
notification, the types of genetically engineered plants that had
industrial uses were typically those in which nutritional components,
such as oil content, were being engineered. Since APHIS had significant
regulatory experience with the types of traits then being introduced
into these plants, industrial plants were eligible for the notification
option. In contrast, the notification regulations in Sec.
340.3(b)(4)(iii) prohibited the use of notification for introductions
of plants genetically engineered to encode compounds for pharmaceutical
use, thus continuing to require a permit for such introductions,
because of our lack of regulatory experience and scientific familiarity
with these types of introduced traits.
In 2003, we noted that a number of more recent introductions of
plants engineered to produce compounds intended for industrial use had
been for traits different than what we were seeing in 1993. Those more
recent introductions were for non-food, non-feed traits with which
APHIS has little regulatory experience or scientific familiarity. Based
on the expansion of the technology and the new non-food, non-feed uses
of industrial plants being developed, we believed it to be prudent and
necessary to remove the notification option for all industrials pending
the completion of our ongoing review of part 340.
Therefore, in an interim rule effective and published in the
Federal Register on August 6, 2003 (68 FR 46434-46436, Docket No. 03-
038-1), we amended the regulations to require that introductions of
plants genetically engineered to encode compounds for industrial use be
conducted only under permit. For purposes of the interim rule, plants
engineered to produce industrial compounds include those plants that
meet the following three criteria: (1) The plants are engineered to
produce compounds that are new to the plant; (2) the new compound has
not been commonly used in food or feed; and (3) the new compound is
being expressed for non-food, non-feed industrial uses. Industrial uses
include, but are not limited to, detergent manufacturing, paper
production, and mineral recovery.
Comments on the interim rule were required to be received on or
before October 6, 2003. We received 12 comments by that date. The
comments were from companies and organizations involved in
biotechnology, an organic certification service, a university
biologist, a private citizen, an association of crop production and
protection companies, and associations representing food producers,
processors, and manufacturers. One of the commenters voiced opposition
to genetically modified plants generally, but offered no specific
comments relating to the interim rule. The remaining commenters
expressed their support for the interim rule, although several made
specific suggestions or
[[Page 23010]]
raised related issues. Those comments are discussed below.
Several commenters raised issues related to the potential for
plants engineered to produce industrial compounds to contaminate or
adulterate food crops. Some commenters urged APHIS to require that the
introduction of such crops be conducted under conditions of 100 percent
containment (e.g., in secure greenhouses) or geographic isolation to
ensure that adulteration does not occur. Other commenters stated that
APHIS should not allow food crops to be genetically modified to produce
industrial compounds in order to eliminate the potential for the spread
of transgenic pollen to sexually compatible non-modified plants. One of
these commenters further suggested that if food crops are to be used to
produce industrial compounds, self-pollinating crops should be used to
the maximum extent possible.
APHIS wishes to reiterate that the purpose of the interim rule was
to ensure that introductions of plants engineered to produce industrial
compounds will be conducted under permit rather than under
notification. Although there are administrative differences between
these procedures, the goal of each is to ensure that plants are
confined during movement and field testing and do not persist in the
environment, and both are designed to achieve high levels of safety. In
addition, use of any regulated article originating from a field test as
food or feed would be subject to the regulatory authority of the Food
and Drug Administration (FDA). Failure to meet any of the requirements
associated with APHIS permits and notifications can lead to substantial
fines, as provided in the Plant Protection Act.
One commenter agreed with the three criteria set out in the interim
rule to describe plants engineered to produce industrial compounds, but
suggested that food or feed plants genetically engineered to produce
dietary supplements that are acceptable only in dietary supplements
should also be considered industrial plants and thus ineligible for
introduction using the notification option.
Plants, whether genetically engineered or not, yield a variety of
compounds that are used to produce dietary supplements. If a food or
feed plant naturally produces a compound used in dietary supplements,
and that plant has been genetically engineered to produce more of that
compound, then that plant would not be considered an industrial plant
(and thus would be eligible for introduction using notification)
because the first of the three criteria is that ``the plants are
engineered to produce compounds that are new to the plant.'' However,
if the compound is new to the plant, has not been commonly used in food
or feed, and is being expressed for non-food, non-feed industrial uses,
then the plant would be considered an industrial plant under our
criteria and thus eligible for introduction only under permit.
Again with respect to the three criteria, one commenter suggested
that APHIS may wish to clarify those criteria regarding the
circumstances under which a permit will and will not be required for
field testing and to provide examples of both to assist the public and
those developing industrial proteins in better understanding those
circumstances.
APHIS may, when needed, provide additional written guidance
illustrating the criteria that define whether a field test qualifies
for the notification procedure or if it must be conducted under permit.
The agency has provided such written guidance since the implementation
of the regulations in part 340 in 1987, offering additional examples
that would not necessarily be appropriate for inclusion in the
regulations themselves and updating or clarifying that guidance as
necessary. When the notification option was added to the regulations in
1993, APHIS published a user's guide to notifications. Copies of our
user's guides are available in print form and may be viewed on the
Agency Web site at https://www.aphis.usda.gov/brs.
One commenter stated that, while it may be currently necessary to
require that introductions of industrial plants be conducted only under
permit, over time APHIS should gain sufficient familiarity with certain
industrial compounds to allow plants producing such compounds to be
grown under notification procedures. The commenter urged APHIS to adopt
this approach as it considers amending its regulations in 7 CFR part
340.
APHIS continually evaluates its regulations in the light of
increased experience and familiarity with scientific, technical, and
administrative considerations. In this or any other situation, the
accumulation of experience or the availability of additional
information may lead us to initiate rulemaking to update the
regulations.
Another commenter, also with an eye toward future amendments to the
regulations, suggested that APHIS provide for enhanced oversight for
industrial plants in the areas of confinement controls, site security,
and compliance verification and the use of third-party auditors,
standard-setting organizations, and standard operating procedures as a
quality control mechanism.
APHIS agrees that it is appropriate to take the considerations
identified by the commenter into account as we continue to review our
existing regulations in part 340 and develop potential amendments to
those regulations.
Continuing Effect of Amendment
The preamble of the interim rule stated that our amendment to the
regulations in part 340 to remove the notification options for plants
genetically engineered to encode compounds for industrial use would be
in effect until December 31, 2004. At the time we made that statement,
and as we explained in the interim rule, it was our intent to remove
the notification option for all industrials pending the completion of
our ongoing review of part 340. That review, which is not yet complete,
is being conducted as part of our consideration of possible amendments
to the regulations to, among other things, include genetically
engineered organisms that may pose a noxious weed risk and genetically
engineered biological control agents.
On January 23, 2004, we published a notice in the Federal Register
(69 FR 3271-3272, Docket No. 03-031-2), in which we advised the public
that we intend to prepare an environmental impact statement (EIS) in
connection with potential changes to the regulations regarding the
importation, interstate movement, and environmental release of certain
genetically engineered organisms. The notice identified potential
issues and alternatives that will be studied in the EIS and requested
public comment to further delineate the scope of the issues and
alternatives.
We believe that it is essential that we consider the findings of
the EIS as part of our review of the existing regulations in part 340,
but the EIS is not yet at a stage at which we may do so. Therefore,
consistent with our stated intent to remove the notification option for
all industrials pending the completion of our review of part 340, we
are announcing that the current requirement that introductions of
plants genetically engineered to encode compounds for industrial use be
conducted only under permit will continue in effect beyond December 31,
2004, until the completion of our review of the regulations in part
340. We expect that our review will include the publication in the
Federal Register of a proposed rule for public comment and
[[Page 23011]]
the subsequent publication of a final rule.
Therefore, for the reasons given in the interim rule and in this
document, we are adopting the interim rule as a final rule without
change.
This action also affirms the information contained in the interim
rule concerning Executive Order 12866 and the Regulatory Flexibility
Act, Executive Orders 12372 and 12988, and the Paperwork Reduction Act.
Further, this action has been determined to be significant for the
purposes of Executive Order 12866 and, therefore, has been reviewed by
the Office of Management and Budget.
List of Subjects in 7 CFR Part 340
Administrative practice and procedure, Biotechnology, Genetic
engineering, Imports, Packaging and containers, Plant diseases and
pests, Transportation.
PART 340--INTRODUCTION OF ORGANISMS AND PRODUCTS ALTERED OR
PRODUCED THROUGH GENETIC ENGINEERING WHICH ARE PLANT PESTS OR WHICH
THERE IS REASON TO BELIEVE ARE PLANT PESTS
0
Accordingly, we are adopting as a final rule, without change, the
interim rule that amended 7 CFR part 340 and that was published at 68
FR 46434-46436 on August 6, 2003.
Done in Washington, DC, this 28th day of April 2005 .
Bill Hawks,
Under Secretary for Marketing and Regulatory Programs.
[FR Doc. 05-8860 Filed 5-3-05; 8:45 am]
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