FIFRA Scientific Advisory Panel; Notice of Public Meeting, 4216-4218 [E8-1191]
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Federal Register / Vol. 73, No. 16 / Thursday, January 24, 2008 / Notices
EPA requested the public to provide
EPA with any significant data or
information that might impact the 3
TMDLs at Federal Register Notice:
Volume 72, Number 241, pages 71409—
71410 (December 17, 2007). No
comments were received.
Dated: January 14, 2008.
William K. Honker,
P.E., Deputy Director, Water Quality
Protection Division, EPA Region 6.
[FR Doc. E8–1195 Filed 1–23–08; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2008–0012; FRL–8348–6]
FIFRA Scientific Advisory Panel;
Notice of Public Meeting
Environmental Protection
Agency (EPA).
ACTION: Notice.
jlentini on PROD1PC65 with NOTICES
AGENCY:
SUMMARY: There will be a 4–day meeting
of the Federal Insecticide, Fungicide,
and Rodenticide Act Scientific Advisory
Panel (FIFRA SAP) to consider and
review the Endocrine Disruptor
Screening Program (EDSP) Proposed
Tier-1 Screening Battery.
DATES: The meeting will be held on
March 25–28, 2008, from approximately
8:30 a.m. to 5:00 p.m, Eastern Standard
Time.
Comments. The Agency encourages
written comments be submitted by
March 11, 2008 and requests for oral
comments be submitted by March 18,
2008. Written comments and requests to
make oral comments are accepted until
the date of the meeting but anyone
submitting written comments after
March 11, 2008 should contact the
Designated Federal Official (DFO) listed
under FOR FURTHER INFORMATION
CONTACT. For additional instructions,
see Unit I.C. of the SUPPLEMENTARY
INFORMATION.
Nominations. Nominations of
candidates to serve as ad hoc members
of the FIFRA SAP for this meeting
should be provided on or before
February 7, 2008.
Special accommodations. For
information on access or services for
individuals with disabilities, and to
request accommodation of a disability,
please contact the DFO listed under FOR
FURTHER INFORMATION CONTACT at least
10 days prior to the meeting to give EPA
as much time as possible to process
your request.
ADDRESSES: The meeting will be held at
the Environmental Protection Agency,
Conference Center - Lobby Level, One
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20:35 Jan 23, 2008
Jkt 214001
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, Virginia 22202.
Comments. Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2008–0012, by
one of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• Mail: Office of Pesticide Programs
(OPP) Regulatory Public Docket (7502P),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW, Washington,
DC 20460–0001.
• Delivery: OPP Regulatory Public
Docket (7502P), Environmental
Protection Agency, Rm. S–4400, One
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket’s
normal hours of operation (8:30 a.m. to
4 p.m., Monday through Friday,
excluding legal holidays). Special
arrangements should be made for
deliveries of boxed information. The
Docket Facility telephone number is
(703) 305–5805.
Instructions. Direct your comments to
docket ID number EPA–HQ–OPP–2008–
0012. If your comments contain any
information that you consider to be CBI
or otherwise protected, please contact
the DFO listed under FOR FURTHER
INFORMATION CONTACT to obtain special
instructions before submitting your
comments. EPA’s policy is that all
comments received will be included in
the docket without change and may be
made available on-line at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through regulations.gov or email. The regulations.gov website is an
‘‘anonymous access’’ system, which
means EPA will not know your identity
or contact information unless you
provide it in the body of your comment.
If you send an e-mail comment directly
to EPA without going through
regulations.gov, your e-mail address
will be automatically captured and
included as part of the comment that is
placed in the docket and made available
on the Internet. If you submit an
electronic comment, EPA recommends
that you include your name and other
contact information in the body of your
comment and with any disk or CD-ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
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the use of special characters, any form
of encryption, and be free of any defects
or viruses.
Docket. All documents in the docket
are listed in a docket index available in
regulations.gov. To access the electronic
docket, go to https://
www.regulations.gov, select ‘‘Advanced
Search,’’ then ‘‘Docket Search.’’ Insert
the docket ID number where indicated
and select the ‘‘Submit’’ button. Follow
the instructions on the regulations.gov
website to view the docket index or
access available documents. Although
listed in a docket index, some
information is not publicly available,
e.g., CBI or other information whose
disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available in the electronic docket at
https://www.regulations.gov, or, if only
available in hard copy, at the OPP
Regulatory Public Docket in Rm. S–
4400, One Potomac Yard (South Bldg.),
2777 S. Crystal Dr., Arlington, VA. The
hours of operation of this Docket
Facility are from 8:30 a.m. to 4 p.m.,
Monday through Friday, excluding legal
holidays. The Docket Facility telephone
number is (703) 305–5805.
Nominations: Nominations, requests
to present oral comments, and requests
for special accommodations. Submit
nominations to serve as an ad hoc
member of the FIFRA SAP, requests for
special seating accommodations, or
requests to present oral comments to the
DFO listed under FOR FURTHER
INFORMATION CONTACT.
FOR FURTHER INFORMATION CONTACT: Jim
Downing, DFO, Office of Science
Coordination and Policy (7201M),
Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington,
DC 20460–0001; telephone number:
(202) 564–8432; fax number: (202) 564–
8382; e-mail addresses:
downing.jim@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed to the public
in general. This action may, however, be
of particular interest to persons who are
or may be required to conduct testing of
chemical substances under the Federal
Food, Drug, and Cosmetic Act (FFDCA),
FIFRA, and the Food Quality Protection
Act of 1996 (FQPA). Since other entities
may also be interested, the Agency has
not attempted to describe all the specific
entities that may be affected by this
action. If you have any questions
E:\FR\FM\24JAN1.SGM
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Federal Register / Vol. 73, No. 16 / Thursday, January 24, 2008 / Notices
regarding the applicability of this action
to a particular entity, consult the DFO
listed under FOR FURTHER INFORMATION
CONTACT.
jlentini on PROD1PC65 with NOTICES
B. What Should I Consider as I Prepare
My Comments for EPA?
When submitting comments,
remember to:
1. Identify the document by docket ID
number and other identifying
information (subject heading, Federal
Register date and page number).
2. Follow directions. The Agency may
ask you to respond to specific questions
or organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
3. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
4. Describe any assumptions and
provide any technical information and/
or data that you used.
5. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
6. Provide specific examples to
illustrate your concerns and suggest
alternatives.
7. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
8. Make sure to submit your
comments by the comment period
deadline identified.
C. How May I Participate in this
Meeting?
You may participate in this meeting
by following the instructions in this
unit. To ensure proper receipt by EPA,
it is imperative that you identify docket
ID number EPA–HQ–OPP–2008–0012 in
the subject line on the first page of your
request.
1. Written comments. The Agency
encourages that written comments be
submitted, using the instructions in
ADDRESSES, no later than March 11,
2008, to provide FIFRA SAP the time
necessary to consider and review the
written comments. Written comments
are accepted until the date of the
meeting but anyone submitting written
comments after March 11, 2008 should
contact the DFO listed under FOR
FURTHER INFORMATION CONTACT. Anyone
submitting written comments at the
meeting should bring 30 copies for
distribution to the FIFRA SAP.
2. Oral comments. The Agency
encourages that each individual or
group wishing to make brief oral
comments to FIFRA SAP submit their
request to the DFO listed under FOR
FURTHER INFORMATION CONTACT no later
than March 18, 2008, in order to be
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20:35 Jan 23, 2008
Jkt 214001
included on the meeting agenda.
Requests to present oral comments will
be accepted until the date of the meeting
and, to the extent that time permits, the
Chair of the FIFRA SAP may permit the
presentation of oral comments at the
meeting by interested persons who have
not previously requested time. The
request should identify the name of the
individual making the presentation, the
organization (if any) the individual will
represent, and any requirements for
audiovisual equipment (e.g., overhead
projector, 35 mm projector, chalkboard).
Oral comments before FIFRA SAP are
limited to approximately 5 minutes
unless prior arrangements have been
made. In addition, each speaker should
bring 30 copies of his or her comments
and presentation slides for distribution
to the FIFRA SAP at the meeting.
3. Seating at the meeting. Seating at
the meeting will be open and on a firstcome basis.
4. Request for nominations to serve as
ad hoc members of the FIFRA SAP for
this meeting. As part of a broader
process for developing a pool of
candidates for each meeting, the FIFRA
SAP staff routinely solicits the
stakeholder community for nominations
of prospective candidates for service as
ad hoc members of the FIFRA SAP. Any
interested person or organization may
nominate qualified individuals to be
considered as prospective candidates for
a specific meeting. Individuals
nominated for this meeting should have
expertise in one or more of the
following areas: Endocrinology,
toxicology, aquatic toxicology, thyroid
biology, reproductive or developmental
toxicology/endocrinology, comparative
endocrinology, and toxicological
pathology. Nominees should be
scientists who have sufficient
professional qualifications, including
training and experience, to be capable of
providing expert comments on the
scientific issues for this meeting.
Nominees should be identified by name,
occupation, position, address, and
telephone number. Nominations should
be provided to the DFO listed under FOR
FURTHER INFORMATION CONTACT on or
before February 7, 2008. The Agency
will consider all nominations of
prospective candidates for this meeting
that are received on or before this date.
However, final selection of ad hoc
members for this meeting is a
discretionary function of the Agency.
The selection of scientists to serve on
the FIFRA SAP is based on the function
of the panel and the expertise needed to
address the Agency’s charge to the
panel. No interested scientists shall be
ineligible to serve by reason of their
membership on any other advisory
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4217
committee to a Federal department or
agency or their employment by a
Federal department or agency except the
EPA. Other factors considered during
the selection process include
availability of the potential panel
member to fully participate in the
panel’s reviews, absence of any conflicts
of interest or appearance of lack of
impartiality, independence with respect
to the matters under review, and lack of
bias. Although financial conflicts of
interest, the appearance of lack of
impartiality, lack of independence, and
bias may result in disqualification, the
absence of such concerns does not
assure that a candidate will be selected
to serve on the FIFRA SAP. Numerous
qualified candidates are identified for
each panel. Therefore, selection
decisions involve carefully weighing a
number of factors including the
candidates’ areas of expertise and
professional qualifications and
achieving an overall balance of different
scientific perspectives on the panel.
In order to have the collective breadth
of experience needed to address the
Agency’s charge for this meeting, the
Agency anticipates selecting
approximately 15 to 20 ad hoc
scientists. FIFRA SAP members are
subject to the provisions of 5 CFR part
2634, Executive Branch Financial
Disclosure, as supplemented by the EPA
in 5 CFR part 6401. In anticipation of
this requirement, prospective
candidates for service on the FIFRA
SAP will be asked to submit
confidential financial information
which shall fully disclose, among other
financial interests, the candidate’s
employment, stocks and bonds, and
where applicable, sources of research
support. The EPA will evaluate the
candidates financial disclosure form to
assess whether there are financial
conflicts of interest, appearance of a
lack of impartiality or any prior
involvement with the development of
the documents under consideration
(including previous scientific peer
review) before the candidate is
considered further for service on the
FIFRA SAP. Those who are selected
from the pool of prospective candidates
will be asked to attend the public
meetings and to participate in the
discussion of key issues and
assumptions at these meetings. In
addition, they will be asked to review
and to help finalize the meeting
minutes. The list of FIFRA SAP
members participating at this meeting
will be posted on the FIFRA SAP
website at https://www.epa.gov/scipoly/
sap or may be obtained from the OPP
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Federal Register / Vol. 73, No. 16 / Thursday, January 24, 2008 / Notices
Regulatory Public Docket at https://
www.regulations.gov.
II. Background
jlentini on PROD1PC65 with NOTICES
A. Purpose of the FIFRA SAP
The FIFRA SAP serves as the primary
scientific peer review mechanism of
EPA’s Office of Prevention, Pesticides
and Toxic Substances (OPPTS) and is
structured to provide scientific advice,
information and recommendations to
the EPA Administrator on pesticides
and pesticide-related issues as to the
impact of regulatory actions on health
and the environment. The FIFRA SAP is
a Federal advisory committee
established in 1975 under FIFRA that
operates in accordance with
requirements of the Federal Advisory
Committee Act. The FIFRA SAP is
composed of a permanent panel
consisting of seven members who are
appointed by the EPA Administrator
from nominees provided by the National
Institutes of Health and the National
Science Foundation. FIFRA, as
amended by FQPA, established a
Science Review Board consisting of at
least 60 scientists who are available to
the Scientific Advisory Panel on an ad
hoc basis to assist in reviews conducted
by the Scientific Advisory Panel. As a
peer review mechanism, the FIFRA SAP
provides comments, evaluations and
recommendations to improve the
effectiveness and quality of analyses
made by Agency scientists. Members of
the FIFRA SAP are scientists who have
sufficient professional qualifications,
including training and experience, to
provide expert advice and
recommendations to the Agency.
B. Public Meeting
The EPA is implementing an
Endocrine Disruptor Screening Program
(EDSP) in response to a 1996
Congressional mandate under the
Federal Food, Drug, and Cosmetic Act
(FFDCA). Section 408(p) of the FFDCA
required the EPA ‘‘to develop a
screening program, using appropriate
validated test systems and other
scientifically relevant information, to
determine whether certain substances
may have an effect in humans that is
similar to an effect produced by a
naturally occurring estrogen, or other
such endocrine effect as EPA may
designate (FFDCA 21 U.S.C. 346a(p). In
1998, the Endocrine Disruptor
Screening and Testing Advisory
Committee (EDSTAC), a panel of experts
chartered pursuant to the Federal
Advisory Committee Act (FACA) in
response to the FFDCA, submitted a
final report to advise the EPA on how
to develop its Endocrine Disruptor
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screening and testing program. The
screening program was also reviewed
and reported on by the EPA’s Science
Advisory Board and Scientific Advisory
Panel (SAB/SAP) as required by the
FFDCA. Together, the EDSTAC and
SAB/SAP recommended that the EPA
address both human and ecological
effects and examine effects on the
estrogen as well as the androgen and
thyroid (EAT) hormonal systems, and
that a two-tiered approach be used for
screening (EPA. Endocrine Disruptor
Screening and Testing Advisory
Committee EDSTAC Final Report.
August 1998.https://www.epa.gov/
scipoly/oscpendo/pubs/edspoverview/
finalrpt.htm). The purpose of Tier-1 is to
identify substances that have the
potential to interact with the EAT
hormonal systems using a battery of
screening assays. The purpose of Tier 2
testing is to identify and establish a
dose-response relationship for any
adverse effects that might result from
the interactions identified through the
Tier-1 screening battery.
The EPA has validated (or anticipates
completing validation in 2008) several
candidate assays for the Tier-1 battery as
follows:
Screening assays being considered for
the Tier-1 battery:
In vitro
• Rat uterine cytosol and human
recombinant estrogen receptor (ER)
binding*
• Rat prostate cytosol androgen
receptor (AR) binding
• Human cell line (H295R)
steroidogenesis*
• Human placental and recombinant
aromatase
In vivo
• Uterotrophic (rat)
• Hershberger (rat)
• Pubertal female (rat)
• Pubertal male (rat)
• Adult male (rat)
• Amphibian metamorphosis (frog)
• Fish short-term reproduction
*Consideration of these assays will be
contingent on individual assay peer
review, which is expected in 2008.
Following an extensive validation
process, the EPA has had (or expects to
have in 2008) each of these assays peer
reviewed independently by a panel of
scientific experts. The individual assay
peer review process was done to ensure
that independent scientific opinions
about the candidate assays were
obtained and considered. Information
regarding individual assay peer review
can be found in section IV.D. of the
Federal Register of July 13, 2007, https://
www.epa.gov/fedrgstr/EPA-PEST/2007/
July/Day-13/p13672.pdf.
The EPA is now convening an
independent scientific peer review of
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the Tier-1 screening battery and has
chosen the FIFRA SAP process. The
FIFRA SAP will be charged with
commenting on whether the EPA’s
proposed battery composition fulfills its
purpose (i.e., to identify the potential to
interact with the EAT hormone
systems). The SAP will specifically be
asked to comment on the strengths and
limitations of the proposed battery, and
to suggest improvements that could be
made to the proposed battery
considering candidate assays. The SAP’s
advice will inform the EPA’s final
decision on the composition of the
EDSP’s Tier-1 screening battery.
C. FIFRA SAP Documents and Meeting
Minutes
EPA’s background paper, related
supporting materials, charge/questions
to the FIFRA SAP, FIFRA SAP
composition (i.e., members and ad hoc
members for this meeting), and the
meeting agenda will be available by late
February 2008. In addition, the Agency
may provide additional background
documents as the materials become
available. You may obtain electronic
copies of these documents, and certain
other related documents that might be
available electronically, at https://
www.regulations.gov and the FIFRA
SAP homepage at https://www.epa.gov/
scipoly/sap.
The FIFRA SAP will prepare meeting
minutes summarizing its
recommendations to the Agency
approximately 90 days after the
meeting. The meeting minutes will be
posted on the FIFRA SAP website or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
List of Subjects
Environmental protection, pesticides
and pests.
January 17, 2008.
Elizabeth Resek,
Acting Director, Office of Science
Coordination and Policy.
[FR Doc. E8–1191 Filed 1–23–08; 8:45 am]
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[CG Docket No. 03–123; DA 07–5009]
The Consumer & Governmental Affairs
Bureau Reports on the First Triennial
Review of the Commission’s Policies
and Practices Under Section 504 of the
Rehabilitation Act of 1973
Federal Communications
Commission.
AGENCY:
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[Federal Register Volume 73, Number 16 (Thursday, January 24, 2008)]
[Notices]
[Pages 4216-4218]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-1191]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2008-0012; FRL-8348-6]
FIFRA Scientific Advisory Panel; Notice of Public Meeting
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: There will be a 4-day meeting of the Federal Insecticide,
Fungicide, and Rodenticide Act Scientific Advisory Panel (FIFRA SAP) to
consider and review the Endocrine Disruptor Screening Program (EDSP)
Proposed Tier-1 Screening Battery.
DATES: The meeting will be held on March 25-28, 2008, from
approximately 8:30 a.m. to 5:00 p.m, Eastern Standard Time.
Comments. The Agency encourages written comments be submitted by
March 11, 2008 and requests for oral comments be submitted by March 18,
2008. Written comments and requests to make oral comments are accepted
until the date of the meeting but anyone submitting written comments
after March 11, 2008 should contact the Designated Federal Official
(DFO) listed under FOR FURTHER INFORMATION CONTACT. For additional
instructions, see Unit I.C. of the SUPPLEMENTARY INFORMATION.
Nominations. Nominations of candidates to serve as ad hoc members
of the FIFRA SAP for this meeting should be provided on or before
February 7, 2008.
Special accommodations. For information on access or services for
individuals with disabilities, and to request accommodation of a
disability, please contact the DFO listed under FOR FURTHER INFORMATION
CONTACT at least 10 days prior to the meeting to give EPA as much time
as possible to process your request.
ADDRESSES: The meeting will be held at the Environmental Protection
Agency, Conference Center - Lobby Level, One Potomac Yard (South
Bldg.), 2777 S. Crystal Dr., Arlington, Virginia 22202.
Comments. Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2008-0012, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
Mail: Office of Pesticide Programs (OPP) Regulatory
Public Docket (7502P), Environmental Protection Agency, 1200
Pennsylvania Ave., NW, Washington, DC 20460-0001.
Delivery: OPP Regulatory Public Docket (7502P),
Environmental Protection Agency, Rm. S-4400, One Potomac Yard (South
Bldg.), 2777 S. Crystal Dr., Arlington, VA. Deliveries are only
accepted during the Docket's normal hours of operation (8:30 a.m. to 4
p.m., Monday through Friday, excluding legal holidays). Special
arrangements should be made for deliveries of boxed information. The
Docket Facility telephone number is (703) 305-5805.
Instructions. Direct your comments to docket ID number EPA-HQ-OPP-
2008-0012. If your comments contain any information that you consider
to be CBI or otherwise protected, please contact the DFO listed under
FOR FURTHER INFORMATION CONTACT to obtain special instructions before
submitting your comments. EPA's policy is that all comments received
will be included in the docket without change and may be made available
on-line at https://www.regulations.gov, including any personal
information provided, unless the comment includes information claimed
to be Confidential Business Information (CBI) or other information
whose disclosure is restricted by statute. Do not submit information
that you consider to be CBI or otherwise protected through
regulations.gov or e-mail. The regulations.gov website is an
``anonymous access'' system, which means EPA will not know your
identity or contact information unless you provide it in the body of
your comment. If you send an e-mail comment directly to EPA without
going through regulations.gov, your e-mail address will be
automatically captured and included as part of the comment that is
placed in the docket and made available on the Internet. If you submit
an electronic comment, EPA recommends that you include your name and
other contact information in the body of your comment and with any disk
or CD-ROM you submit. If EPA cannot read your comment due to technical
difficulties and cannot contact you for clarification, EPA may not be
able to consider your comment. Electronic files should avoid the use of
special characters, any form of encryption, and be free of any defects
or viruses.
Docket. All documents in the docket are listed in a docket index
available in regulations.gov. To access the electronic docket, go to
https://www.regulations.gov, select ``Advanced Search,'' then ``Docket
Search.'' Insert the docket ID number where indicated and select the
``Submit'' button. Follow the instructions on the regulations.gov
website to view the docket index or access available documents.
Although listed in a docket index, some information is not publicly
available, e.g., CBI or other information whose disclosure is
restricted by statute. Certain other material, such as copyrighted
material, is not placed on the Internet and will be publicly available
only in hard copy form. Publicly available docket materials are
available in the electronic docket at https://www.regulations.gov, or,
if only available in hard copy, at the OPP Regulatory Public Docket in
Rm. S-4400, One Potomac Yard (South Bldg.), 2777 S. Crystal Dr.,
Arlington, VA. The hours of operation of this Docket Facility are from
8:30 a.m. to 4 p.m., Monday through Friday, excluding legal holidays.
The Docket Facility telephone number is (703) 305-5805.
Nominations: Nominations, requests to present oral comments, and
requests for special accommodations. Submit nominations to serve as an
ad hoc member of the FIFRA SAP, requests for special seating
accommodations, or requests to present oral comments to the DFO listed
under FOR FURTHER INFORMATION CONTACT.
FOR FURTHER INFORMATION CONTACT: Jim Downing, DFO, Office of Science
Coordination and Policy (7201M), Environmental Protection Agency, 1200
Pennsylvania Ave., NW., Washington, DC 20460-0001; telephone number:
(202) 564-8432; fax number: (202) 564-8382; e-mail addresses:
downing.jim@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this Action Apply to Me?
This action is directed to the public in general. This action may,
however, be of particular interest to persons who are or may be
required to conduct testing of chemical substances under the Federal
Food, Drug, and Cosmetic Act (FFDCA), FIFRA, and the Food Quality
Protection Act of 1996 (FQPA). Since other entities may also be
interested, the Agency has not attempted to describe all the specific
entities that may be affected by this action. If you have any questions
[[Page 4217]]
regarding the applicability of this action to a particular entity,
consult the DFO listed under FOR FURTHER INFORMATION CONTACT.
B. What Should I Consider as I Prepare My Comments for EPA?
When submitting comments, remember to:
1. Identify the document by docket ID number and other identifying
information (subject heading, Federal Register date and page number).
2. Follow directions. The Agency may ask you to respond to
specific questions or organize comments by referencing a Code of
Federal Regulations (CFR) part or section number.
3. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
4. Describe any assumptions and provide any technical information
and/or data that you used.
5. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
6. Provide specific examples to illustrate your concerns and
suggest alternatives.
7. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
8. Make sure to submit your comments by the comment period deadline
identified.
C. How May I Participate in this Meeting?
You may participate in this meeting by following the instructions
in this unit. To ensure proper receipt by EPA, it is imperative that
you identify docket ID number EPA-HQ-OPP-2008-0012 in the subject line
on the first page of your request.
1. Written comments. The Agency encourages that written comments be
submitted, using the instructions in ADDRESSES, no later than March 11,
2008, to provide FIFRA SAP the time necessary to consider and review
the written comments. Written comments are accepted until the date of
the meeting but anyone submitting written comments after March 11, 2008
should contact the DFO listed under FOR FURTHER INFORMATION CONTACT.
Anyone submitting written comments at the meeting should bring 30
copies for distribution to the FIFRA SAP.
2. Oral comments. The Agency encourages that each individual or
group wishing to make brief oral comments to FIFRA SAP submit their
request to the DFO listed under FOR FURTHER INFORMATION CONTACT no
later than March 18, 2008, in order to be included on the meeting
agenda. Requests to present oral comments will be accepted until the
date of the meeting and, to the extent that time permits, the Chair of
the FIFRA SAP may permit the presentation of oral comments at the
meeting by interested persons who have not previously requested time.
The request should identify the name of the individual making the
presentation, the organization (if any) the individual will represent,
and any requirements for audiovisual equipment (e.g., overhead
projector, 35 mm projector, chalkboard). Oral comments before FIFRA SAP
are limited to approximately 5 minutes unless prior arrangements have
been made. In addition, each speaker should bring 30 copies of his or
her comments and presentation slides for distribution to the FIFRA SAP
at the meeting.
3. Seating at the meeting. Seating at the meeting will be open and
on a first-come basis.
4. Request for nominations to serve as ad hoc members of the FIFRA
SAP for this meeting. As part of a broader process for developing a
pool of candidates for each meeting, the FIFRA SAP staff routinely
solicits the stakeholder community for nominations of prospective
candidates for service as ad hoc members of the FIFRA SAP. Any
interested person or organization may nominate qualified individuals to
be considered as prospective candidates for a specific meeting.
Individuals nominated for this meeting should have expertise in one or
more of the following areas: Endocrinology, toxicology, aquatic
toxicology, thyroid biology, reproductive or developmental toxicology/
endocrinology, comparative endocrinology, and toxicological pathology.
Nominees should be scientists who have sufficient professional
qualifications, including training and experience, to be capable of
providing expert comments on the scientific issues for this meeting.
Nominees should be identified by name, occupation, position, address,
and telephone number. Nominations should be provided to the DFO listed
under FOR FURTHER INFORMATION CONTACT on or before February 7, 2008.
The Agency will consider all nominations of prospective candidates for
this meeting that are received on or before this date. However, final
selection of ad hoc members for this meeting is a discretionary
function of the Agency.
The selection of scientists to serve on the FIFRA SAP is based on
the function of the panel and the expertise needed to address the
Agency's charge to the panel. No interested scientists shall be
ineligible to serve by reason of their membership on any other advisory
committee to a Federal department or agency or their employment by a
Federal department or agency except the EPA. Other factors considered
during the selection process include availability of the potential
panel member to fully participate in the panel's reviews, absence of
any conflicts of interest or appearance of lack of impartiality,
independence with respect to the matters under review, and lack of
bias. Although financial conflicts of interest, the appearance of lack
of impartiality, lack of independence, and bias may result in
disqualification, the absence of such concerns does not assure that a
candidate will be selected to serve on the FIFRA SAP. Numerous
qualified candidates are identified for each panel. Therefore,
selection decisions involve carefully weighing a number of factors
including the candidates' areas of expertise and professional
qualifications and achieving an overall balance of different scientific
perspectives on the panel.
In order to have the collective breadth of experience needed to
address the Agency's charge for this meeting, the Agency anticipates
selecting approximately 15 to 20 ad hoc scientists. FIFRA SAP members
are subject to the provisions of 5 CFR part 2634, Executive Branch
Financial Disclosure, as supplemented by the EPA in 5 CFR part 6401. In
anticipation of this requirement, prospective candidates for service on
the FIFRA SAP will be asked to submit confidential financial
information which shall fully disclose, among other financial
interests, the candidate's employment, stocks and bonds, and where
applicable, sources of research support. The EPA will evaluate the
candidates financial disclosure form to assess whether there are
financial conflicts of interest, appearance of a lack of impartiality
or any prior involvement with the development of the documents under
consideration (including previous scientific peer review) before the
candidate is considered further for service on the FIFRA SAP. Those who
are selected from the pool of prospective candidates will be asked to
attend the public meetings and to participate in the discussion of key
issues and assumptions at these meetings. In addition, they will be
asked to review and to help finalize the meeting minutes. The list of
FIFRA SAP members participating at this meeting will be posted on the
FIFRA SAP website at https://www.epa.gov/scipoly/sap or may be obtained
from the OPP
[[Page 4218]]
Regulatory Public Docket at https://www.regulations.gov.
II. Background
A. Purpose of the FIFRA SAP
The FIFRA SAP serves as the primary scientific peer review
mechanism of EPA's Office of Prevention, Pesticides and Toxic
Substances (OPPTS) and is structured to provide scientific advice,
information and recommendations to the EPA Administrator on pesticides
and pesticide-related issues as to the impact of regulatory actions on
health and the environment. The FIFRA SAP is a Federal advisory
committee established in 1975 under FIFRA that operates in accordance
with requirements of the Federal Advisory Committee Act. The FIFRA SAP
is composed of a permanent panel consisting of seven members who are
appointed by the EPA Administrator from nominees provided by the
National Institutes of Health and the National Science Foundation.
FIFRA, as amended by FQPA, established a Science Review Board
consisting of at least 60 scientists who are available to the
Scientific Advisory Panel on an ad hoc basis to assist in reviews
conducted by the Scientific Advisory Panel. As a peer review mechanism,
the FIFRA SAP provides comments, evaluations and recommendations to
improve the effectiveness and quality of analyses made by Agency
scientists. Members of the FIFRA SAP are scientists who have sufficient
professional qualifications, including training and experience, to
provide expert advice and recommendations to the Agency.
B. Public Meeting
The EPA is implementing an Endocrine Disruptor Screening Program
(EDSP) in response to a 1996 Congressional mandate under the Federal
Food, Drug, and Cosmetic Act (FFDCA). Section 408(p) of the FFDCA
required the EPA ``to develop a screening program, using appropriate
validated test systems and other scientifically relevant information,
to determine whether certain substances may have an effect in humans
that is similar to an effect produced by a naturally occurring
estrogen, or other such endocrine effect as EPA may designate (FFDCA 21
U.S.C. 346a(p). In 1998, the Endocrine Disruptor Screening and Testing
Advisory Committee (EDSTAC), a panel of experts chartered pursuant to
the Federal Advisory Committee Act (FACA) in response to the FFDCA,
submitted a final report to advise the EPA on how to develop its
Endocrine Disruptor screening and testing program. The screening
program was also reviewed and reported on by the EPA's Science Advisory
Board and Scientific Advisory Panel (SAB/SAP) as required by the FFDCA.
Together, the EDSTAC and SAB/SAP recommended that the EPA address both
human and ecological effects and examine effects on the estrogen as
well as the androgen and thyroid (EAT) hormonal systems, and that a
two-tiered approach be used for screening (EPA. Endocrine Disruptor
Screening and Testing Advisory Committee EDSTAC Final Report. August
1998.https://www.epa.gov/scipoly/oscpendo/pubs/edspoverview/
finalrpt.htm). The purpose of Tier-1 is to identify substances that
have the potential to interact with the EAT hormonal systems using a
battery of screening assays. The purpose of Tier 2 testing is to
identify and establish a dose-response relationship for any adverse
effects that might result from the interactions identified through the
Tier-1 screening battery.
The EPA has validated (or anticipates completing validation in
2008) several candidate assays for the Tier-1 battery as follows:
Screening assays being considered for the Tier-1 battery:
In vitro
Rat uterine cytosol and human recombinant estrogen
receptor (ER) binding*
Rat prostate cytosol androgen receptor (AR) binding
Human cell line (H295R) steroidogenesis*
Human placental and recombinant aromatase
In vivo
Uterotrophic (rat)
Hershberger (rat)
Pubertal female (rat)
Pubertal male (rat)
Adult male (rat)
Amphibian metamorphosis (frog)
Fish short-term reproduction
*Consideration of these assays will be contingent on individual
assay peer review, which is expected in 2008.
Following an extensive validation process, the EPA has had (or
expects to have in 2008) each of these assays peer reviewed
independently by a panel of scientific experts. The individual assay
peer review process was done to ensure that independent scientific
opinions about the candidate assays were obtained and considered.
Information regarding individual assay peer review can be found in
section IV.D. of the Federal Register of July 13, 2007, https://
www.epa.gov/fedrgstr/EPA-PEST/2007/July/Day-13/p13672.pdf.
The EPA is now convening an independent scientific peer review of
the Tier-1 screening battery and has chosen the FIFRA SAP process. The
FIFRA SAP will be charged with commenting on whether the EPA's proposed
battery composition fulfills its purpose (i.e., to identify the
potential to interact with the EAT hormone systems). The SAP will
specifically be asked to comment on the strengths and limitations of
the proposed battery, and to suggest improvements that could be made to
the proposed battery considering candidate assays. The SAP's advice
will inform the EPA's final decision on the composition of the EDSP's
Tier-1 screening battery.
C. FIFRA SAP Documents and Meeting Minutes
EPA's background paper, related supporting materials, charge/
questions to the FIFRA SAP, FIFRA SAP composition (i.e., members and ad
hoc members for this meeting), and the meeting agenda will be available
by late February 2008. In addition, the Agency may provide additional
background documents as the materials become available. You may obtain
electronic copies of these documents, and certain other related
documents that might be available electronically, at https://
www.regulations.gov and the FIFRA SAP homepage at https://www.epa.gov/
scipoly/sap.
The FIFRA SAP will prepare meeting minutes summarizing its
recommendations to the Agency approximately 90 days after the meeting.
The meeting minutes will be posted on the FIFRA SAP website or may be
obtained from the OPP Regulatory Public Docket at https://
www.regulations.gov.
List of Subjects
Environmental protection, pesticides and pests.
January 17, 2008.
Elizabeth Resek,
Acting Director, Office of Science Coordination and Policy.
[FR Doc. E8-1191 Filed 1-23-08; 8:45 am]
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