FIFRA Scientific Advisory Panel; Notice of Public Meeting, 76457-76460 [2010-30630]
Download as PDF
Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
part of the EPA registration numbers of
the products listed above.
TABLE 2—REGISTRANTS OF
METHOMYL PRODUCTS
EPA company
No.
Company name and address
000352 ...........
E.I. du Pont de Nemours
and Company DuPont
Crop Protection, StineHaskell Research Center,
P.O. Box 30, Newark, DE
19714–0030.
III. Summary of Public Comments
Received and Agency Response to
Comments
On April 14, 2008, during the public
comment period the registrant withdrew
the voluntary cancellation of the grape
use and submitted a PRIA action
consisting of a change in the use of
methomyl on grapes along with grape
residue monitoring data provided by
grape growers. While this new
information refined the dietary
assessment, it was not sufficient to
change the Agency’s previous
conclusion. As a result, the registrant
withdrew the PRIA action on April 9,
2010. For this reason, the Agency does
not believe that the information
submitted during the comment period
merits further review or a denial of the
requests for voluntary use deletion.
IV. Cancellation Order
Pursuant to FIFRA section 6(f), EPA
hereby approves the requested
amendments to terminate uses of
methomyl registrations identified in
Table 1 of Unit II. Accordingly, the
Agency hereby orders that the product
registrations identified in Table 1 of
Unit II. are amended to terminate the
affected use. The effective date of the
cancellations that are the subject of this
notice is December 8, 2010. Any
distribution, sale, or use of existing
stocks of the products identified in
Table 1 of Unit II. in a manner
inconsistent with any of the provisions
for disposition of existing stocks set
forth in Unit VI. will be a violation of
FIFRA.
jlentini on DSKJ8SOYB1PROD with NOTICES
V. What is the Agency’s authority for
taking this action?
18:23 Dec 07, 2010
Jkt 223001
VI. Provisions for Disposition of
Existing Stocks
Existing stocks are those stocks of
registered pesticide products which are
currently in the United States and
which were packaged, labeled, and
released for shipment prior to the
effective date of the action. The existing
stocks provision for the products subject
to this order is as follows.
Now that EPA has approved product
labels reflecting the requested
amendments to delete uses, registrants
are permitted to sell or distribute
products listed in Table 1 of Unit II.
under the previously approved labeling
until June 8, 2012, a period of 18
months after publication of the
cancellation order in this Federal
Register, unless other restrictions have
been imposed. Thereafter, registrants
will be prohibited from selling or
distributing the products whose labels
include the deleted uses identified in
Table 1 of Unit II., except for export
consistent with FIFRA section 17 or for
proper disposal.
Persons other than the registrant may
sell, distribute, or use existing stocks of
products whose labels include the
deleted uses until supplies are
exhausted, provided that such sale,
distribution, or use is consistent with
the terms of the previously approved
labeling on, or that accompanied,
products with the deleted uses.
List of Subjects
Environmental protection, Pesticides
and pests.
Dated: December 2, 2010.
Richard P. Keigwin, Jr.,
Director, Pesticide Re-evaluation Division,
Office of Pesticide Programs.
[FR Doc. 2010–30865 Filed 12–7–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPP–2010–0588; FRL–8854–5]
Section 6(f)(1) of FIFRA provides that
a registrant of a pesticide product may
at any time request that any of its
pesticide registrations be canceled or
amended to terminate one or more uses.
FIFRA further provides that, before
acting on the request, EPA must publish
a notice of receipt of any such request
in the Federal Register. Thereafter,
VerDate Mar<15>2010
following the public comment period,
the EPA Administrator may approve
such a request. The notice of receipt for
this action was published for comment
on October 24, 2007 (72 FR 60634)
(FRL–8153–3). The comment period
closed on April 21, 2008.
FIFRA Scientific Advisory Panel;
Notice of Public Meeting
Environmental Protection
Agency.
ACTION: Notice.
AGENCY:
There will be a 4–day meeting
of the Federal Insecticide, Fungicide,
SUMMARY:
PO 00000
Frm 00065
Fmt 4703
Sfmt 4703
76457
and Rodenticide Act Scientific Advisory
Panel (FIFRA SAP) to consider and
review the Chlorpyrifos PhysiologicallyBased Pharmacokinetic/
Pharmacodynamic (PBPK/PD) Modeling
linked to the Cumulative and Aggregate
Risk Evaluation System (CARES).
DATES: The meeting will be held on
February 15–18, 2011, from 9 a.m. to
approximately 5:30 p.m.
Comments. The Agency encourages
that written comments be submitted by
January 31, 2011 and requests for oral
comments be submitted by February 8,
2011. However, written comments and
requests to make oral comments may be
submitted until the date of the meeting,
but anyone submitting written
comments after January 31, 2011 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 FIFRA SAP for this meeting should
be provided on or before December 22,
2010.
Webcast. This meeting may be
webcast. Please refer to the FIFRA SAP’s
Web site, https://www.epa.gov/scipoly/
SAP for information on how to access
the webcast. Please note that the
webcast is a supplementary public
process provided only for convenience.
If difficulties arise resulting in
webcasting outages, the meeting will
continue as planned.
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, VA 22202.
Comments. Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPP–2010–0588, 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
E:\FR\FM\08DEN1.SGM
08DEN1
jlentini on DSKJ8SOYB1PROD with NOTICES
76458
Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
Potomac Yard (South Bldg.), 2777 S.
Crystal Dr., Arlington, VA. Deliveries
are only accepted during the Docket
Facility’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–2010–
0588. 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 Web site 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 the docket index available
at https://www.regulations.gov.
Although, listed in the 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 either in the electronic docket
at https://www.regulations.gov, or, if only
VerDate Mar<15>2010
18:23 Dec 07, 2010
Jkt 223001
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, requests to present oral
comments, and requests for special
accommodations. Submit nominations
to serve as ad hoc members of 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:
Sharlene R. Matten, DFO, Office of
Science Coordination and Policy
(7201M), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460–0001; telephone
number: (202) 564–0130; fax number:
(202) 564–8382; e-mail address:
matten.sharlene@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 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
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
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
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–2010–0588 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 January 31,
2011, 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 January 31, 2011,
should contact the DFO listed under FOR
FURTHER INFORMATION CONTACT. Anyone
submitting written comments at the
meeting should bring 30 copies for
distribution to 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 February 8, 2011, 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 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.
E:\FR\FM\08DEN1.SGM
08DEN1
jlentini on DSKJ8SOYB1PROD with NOTICES
Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
4. Request for nominations to serve as
ad hoc members of FIFRA SAP for this
meeting. As part of a broader process for
developing a pool of candidates for each
meeting, FIFRA SAP staff routinely
solicits the stakeholder community for
nominations of prospective candidates
for service as ad hoc members of 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: Risk
assessment, organophosphate
pesticides, cholinesterase inhibition,
data-derived uncertainty factors (also
referred to as chemical-specific
adjustment factors), pharmacodynamic
modeling, physiologically-based
pharmacokinetic modeling,
biomonitoring data, statistical modeling,
probabilistic techniques, and dietary
exposure to pesticides. 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 December 22, 2010. 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
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 FIFRA SAP. Numerous
qualified candidates are identified for
VerDate Mar<15>2010
18:23 Dec 07, 2010
Jkt 223001
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 10–15 ad hoc scientists.
FIFRA SAP members are subject to
the provisions of 5 CFR part 2634,
Executive Branch Financial Disclosure,
as supplemented by 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. 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 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 Web
site at https://epa.gov/scipoly/sap, or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
II. Background
A. Purpose of FIFRA SAP
FIFRA SAP serves as the primary
scientific peer review mechanism of
EPA’s Office of Chemical Safety and
Pollution Prevention (OCSPP) 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. FIFRA SAP is a
Federal advisory committee established
in 1975 under FIFRA that operates in
accordance with requirements of the
Federal Advisory Committee Act. FIFRA
SAP is composed of a permanent panel
consisting of seven members who are
appointed by the EPA Administrator
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
76459
from nominees provided by the National
Institutes of Health and the National
Science Foundation. FIFRA, as
amended by the Food Quality Protection
Act of 1996 (FQPA), established a
Science Review Board consisting of at
least 60 scientists who are available to
the SAP on an ad hoc basis to assist in
reviews conducted by the SAP. As a
peer review mechanism, FIFRA SAP
provides comments, evaluations and
recommendations to improve the
effectiveness and quality of analyses
made by Agency scientists. Members of
FIFRA SAP are scientists who have
sufficient professional qualifications,
including training and experience, to
provide expert advice and
recommendation to the Agency.
B. Public Meeting
Chlorpyrifos (0,0-diethyl-0-3,5,6trichloro-2-pyridyl phosphorothioate) is
a broad-spectrum, chlorinated
organophosphate (OP) insecticide. In
2000, nearly all residential uses were
voluntarily cancelled by Dow
AgroSciences, but agricultural uses
remain. The 2000 human health risk
assessment was largely based on adult
laboratory animal data (rat or dog) for
cholinesterase inhibition and the
application of default uncertainty
factors to address inter- and intraspecies differences including
susceptible populations. Currently, the
Agency is developing a new human
health risk assessment expected to be
released in 2011. In 2008, the FIFRA
Scientific Advisory Panel (SAP)
reviewed a draft science issue paper on
the human health effects of chlorpyrifos.
Since that time, Dow AgroSciences has
undergone a research effort to improve
the existing physiologically-based
pharmacokinetic/pharmacodynamic
model (PBPK/PD) developed by Dr.
Charles Timchalk and co-workers at
Pacific Northwest National Laboratory.
Dow AgroSciences has also developed a
proposed approach for merging this
PBPK/PD model with CARES
Cumulative and Aggregate Risk
Evaluation System, see https://
www.ilsi.org/ResearchFoundation/
Pages/CARES.aspx, a publicallyavailable probabilistic exposure model.
The purpose of the February 2011 SAP
meeting will be to review the PBPK/PD
model and to evaluate the proposed
approach for linking this PBPK model to
the probabilistic exposure model.
The linking of the chlorpyrifos PBPK/
PD model with a probabilistic exposure
model may provide opportunities to
calculate distributions of exposure to
chlorpyrifos and its metabolites with
cholinesterase inhibition levels across
the U.S. population. In addition, this
E:\FR\FM\08DEN1.SGM
08DEN1
76460
Federal Register / Vol. 75, No. 235 / Wednesday, December 8, 2010 / Notices
approach may allow estimation of dataderived uncertainty factors that consider
use of toxicokinetic and toxicodynamic
data to inform quantitative
extrapolations for interspecies
differences and human variability in
dose response assessment. The topics to
be covered in the February 2011 SAP
are consistent with EPA’s Office of
Pesticide Programs continuing efforts to
improve the scientific basis for risk
assessment by broadening the
application of probabilistic exposure
techniques and PBPK models. The
Agency has a conceptually similar effort
on-going to link PBPK models for
pyrethroids with Stochastic Human
Exposure and Dose Simulator (SHEDS)
exposure software, a probabilistic
exposure model developed by the EPA’s
Office of Research and Development,
which was reviewed by the SAP in July
2010. The current effort by Dow
AgroSciences is a research effort which
may, if sufficiently robust, inform future
risk assessments; the February meeting
is a key milestone in this research. The
Agency will solicit feedback from the
Panel on technical issues related to
PBPK/PD model, the proposed approach
for merging the PBPK/PD model with
CARES, and the use of such merged
models in risk assessment.
jlentini on DSKJ8SOYB1PROD with NOTICES
C. FIFRA SAP Documents and Meeting
Minutes
EPA’s background paper, related
supporting materials, charge/questions
to FIFRA SAP, FIFRA SAP composition
(i.e., members and ad hoc members for
this meeting), and the meeting agenda
will be available by late January 2011.
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.
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 Web site or
may be obtained from the OPP
Regulatory Public Docket at https://
www.regulations.gov.
List of Subjects
Environmental protection, Pesticides
and pests.
VerDate Mar<15>2010
18:23 Dec 07, 2010
Jkt 223001
Dated: November 23, 2010.
Frank Sanders,
Director, Office of Science Coordination and
Policy.
[FR Doc. 2010–30630 Filed 12–7–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9236–6; Docket ID No. EPA–HQ–ORD–
2010–0991]
Lymphohematopoietic Cancers
Induced by Chemicals and Other
Agents: Overview and Implications for
Risk Assessment
Environmental Protection
Agency (EPA).
ACTION: Notice of public comment
period.
AGENCY:
EPA is announcing a 45-day
public comment period for the draft
document titled,
‘‘Lymphohematopoietic Cancers
Induced by Chemicals and Other
Agents: Overview and Implications for
Risk Assessment’’ (EPA/600/R–10/
095A). The draft document was
prepared by the National Center for
Environmental Assessment within
EPA’s Office of Research and
Development. The draft document
provides an overview of the types and
mechanisms underlying the
lymphohematopoietic cancers induced
by chemical agents and radiation in
humans, with a primary emphasis on
leukemia and leukemia-inducing agents.
In addition, the document also focuses
on how mechanistic information on
human leukemia-inducing agents can
inform risk assessment.
EPA is releasing this draft document
solely for the purpose of predissemination peer review under
applicable information quality
guidelines. This draft document has not
been formally disseminated by EPA. It
does not represent and should not be
construed to represent any Agency
policy or determination. All public
comments received will be provided to
the peer reviewers at the beginning of
the review process.
DATES: The 45-day public comment
period begins December 8, 2010, and
ends January 24, 2011. Technical
comments should be in writing and
must be received by EPA by January 24,
2011.
ADDRESSES: The draft
‘‘Lymphohematopoietic Cancers
Induced by Chemicals and Other
Agents: Overview and Implications for
Risk Assessment’’ is available primarily
SUMMARY:
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
via the Internet on the National Center
for Environmental Assessment’s home
page under the Recent Additions and
the Data and Publications menus at
https://www.epa.gov/ncea. A limited
number of paper copies are available
from the Information Management
Team, NCEA; telephone: 703–347–8561;
facsimile: 703–347–8691. If you are
requesting a paper copy, please provide
your name, your mailing address, and
the draft document title,
‘‘Lymphohematopoietic Cancers
Induced by Chemicals and Other
Agents: Overview and Implications for
Risk Assessment.’’
Comments may be submitted
electronically via https://
www.regulations.gov, by mail, by
facsimile, or by hand delivery/courier.
Please follow the detailed instructions
provided in the SUPPLEMENTARY
INFORMATION section of this notice.
FOR FURTHER INFORMATION CONTACT: For
information on the public comment
period, contact the Office of
Environmental Information Docket;
telephone: 202–566–1752; facsimile:
202–566–1753; or e-mail:
ORD.Docket@epa.gov.
For technical information, contact
Nagu Keshava, NCEA; telephone: 919–
541–3047; facsimile: 919–541–0245; or
e-mail: keshava.nagu@epa.gov.
SUPPLEMENTARY INFORMATION:
I. Information About the Project/
Document
This project was initiated to better
understand the mechanisms underlying
the lymphohematopoietic cancers
induced by chemical agents in humans.
A draft report was developed that
provides an overview of types and
mechanisms underlying the
lymphohematopoietic cancers induced
by both chemical agents and radiation
in humans, with a primary emphasis on
leukemia and leukemia-inducing agents.
II. How to Submit Technical Comments
to the Docket at https://
www.regulations.gov
Submit your comments, identified by
Docket ID No. EPA–HQ–ORD–2010–
0991, by one of the following methods:
• https://www.regulations.gov: Follow
the on-line instructions for submitting
comments.
• E-mail: ORD.Docket@epa.gov.
• Fax: 202–566–1753.
• Mail: Office of Environmental
Information (OEI) Docket (Mail Code:
2822T), U.S. Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460. The phone
number is 202–566–1752.
• Hand Delivery: The OEI Docket is
located in the EPA Headquarters Docket
E:\FR\FM\08DEN1.SGM
08DEN1
Agencies
[Federal Register Volume 75, Number 235 (Wednesday, December 8, 2010)]
[Notices]
[Pages 76457-76460]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-30630]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OPP-2010-0588; FRL-8854-5]
FIFRA Scientific Advisory Panel; Notice of Public Meeting
AGENCY: Environmental Protection Agency.
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 Chlorpyrifos Physiologically-Based
Pharmacokinetic/Pharmacodynamic (PBPK/PD) Modeling linked to the
Cumulative and Aggregate Risk Evaluation System (CARES).
DATES: The meeting will be held on February 15-18, 2011, from 9 a.m. to
approximately 5:30 p.m.
Comments. The Agency encourages that written comments be submitted
by January 31, 2011 and requests for oral comments be submitted by
February 8, 2011. However, written comments and requests to make oral
comments may be submitted until the date of the meeting, but anyone
submitting written comments after January 31, 2011 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 FIFRA SAP for this meeting should be provided on or before December
22, 2010.
Webcast. This meeting may be webcast. Please refer to the FIFRA
SAP's Web site, https://www.epa.gov/scipoly/SAP for information on how
to access the webcast. Please note that the webcast is a supplementary
public process provided only for convenience. If difficulties arise
resulting in webcasting outages, the meeting will continue as planned.
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, VA 22202.
Comments. Submit your comments, identified by docket identification
(ID) number EPA-HQ-OPP-2010-0588, 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
[[Page 76458]]
Potomac Yard (South Bldg.), 2777 S. Crystal Dr., Arlington, VA.
Deliveries are only accepted during the Docket Facility'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-
2010-0588. 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 Web site 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 the docket index
available at https://www.regulations.gov. Although, listed in the 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 either 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, requests to present oral comments, and requests for
special accommodations. Submit nominations to serve as ad hoc members
of 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: Sharlene R. Matten, DFO, Office of
Science Coordination and Policy (7201M), Environmental Protection
Agency, 1200 Pennsylvania Ave., NW., Washington, DC 20460-0001;
telephone number: (202) 564-0130; fax number: (202) 564-8382; e-mail
address: matten.sharlene@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 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 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-2010-0588 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 January
31, 2011, 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
January 31, 2011, should contact the DFO listed under FOR FURTHER
INFORMATION CONTACT. Anyone submitting written comments at the meeting
should bring 30 copies for distribution to 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 February 8, 2011, 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
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.
[[Page 76459]]
4. Request for nominations to serve as ad hoc members of FIFRA SAP
for this meeting. As part of a broader process for developing a pool of
candidates for each meeting, FIFRA SAP staff routinely solicits the
stakeholder community for nominations of prospective candidates for
service as ad hoc members of 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: Risk assessment, organophosphate pesticides, cholinesterase
inhibition, data-derived uncertainty factors (also referred to as
chemical-specific adjustment factors), pharmacodynamic modeling,
physiologically-based pharmacokinetic modeling, biomonitoring data,
statistical modeling, probabilistic techniques, and dietary exposure to
pesticides. 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
December 22, 2010. 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 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 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 10-15 ad hoc scientists.
FIFRA SAP members are subject to the provisions of 5 CFR part 2634,
Executive Branch Financial Disclosure, as supplemented by 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. 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 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 Web site at https://epa.gov/scipoly/sap, or may be obtained
from the OPP Regulatory Public Docket at https://www.regulations.gov.
II. Background
A. Purpose of FIFRA SAP
FIFRA SAP serves as the primary scientific peer review mechanism of
EPA's Office of Chemical Safety and Pollution Prevention (OCSPP) 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. FIFRA SAP is a Federal advisory committee established in
1975 under FIFRA that operates in accordance with requirements of the
Federal Advisory Committee Act. 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 the
Food Quality Protection Act of 1996 (FQPA), established a Science
Review Board consisting of at least 60 scientists who are available to
the SAP on an ad hoc basis to assist in reviews conducted by the SAP.
As a peer review mechanism, FIFRA SAP provides comments, evaluations
and recommendations to improve the effectiveness and quality of
analyses made by Agency scientists. Members of FIFRA SAP are scientists
who have sufficient professional qualifications, including training and
experience, to provide expert advice and recommendation to the Agency.
B. Public Meeting
Chlorpyrifos (0,0-diethyl-0-3,5,6-trichloro-2-pyridyl
phosphorothioate) is a broad-spectrum, chlorinated organophosphate (OP)
insecticide. In 2000, nearly all residential uses were voluntarily
cancelled by Dow AgroSciences, but agricultural uses remain. The 2000
human health risk assessment was largely based on adult laboratory
animal data (rat or dog) for cholinesterase inhibition and the
application of default uncertainty factors to address inter- and intra-
species differences including susceptible populations. Currently, the
Agency is developing a new human health risk assessment expected to be
released in 2011. In 2008, the FIFRA Scientific Advisory Panel (SAP)
reviewed a draft science issue paper on the human health effects of
chlorpyrifos. Since that time, Dow AgroSciences has undergone a
research effort to improve the existing physiologically-based
pharmacokinetic/pharmacodynamic model (PBPK/PD) developed by Dr.
Charles Timchalk and co-workers at Pacific Northwest National
Laboratory. Dow AgroSciences has also developed a proposed approach for
merging this PBPK/PD model with CARES Cumulative and Aggregate Risk
Evaluation System, see https://www.ilsi.org/ResearchFoundation/Pages/CARES.aspx, a publically-available probabilistic exposure model. The
purpose of the February 2011 SAP meeting will be to review the PBPK/PD
model and to evaluate the proposed approach for linking this PBPK model
to the probabilistic exposure model.
The linking of the chlorpyrifos PBPK/PD model with a probabilistic
exposure model may provide opportunities to calculate distributions of
exposure to chlorpyrifos and its metabolites with cholinesterase
inhibition levels across the U.S. population. In addition, this
[[Page 76460]]
approach may allow estimation of data-derived uncertainty factors that
consider use of toxicokinetic and toxicodynamic data to inform
quantitative extrapolations for interspecies differences and human
variability in dose response assessment. The topics to be covered in
the February 2011 SAP are consistent with EPA's Office of Pesticide
Programs continuing efforts to improve the scientific basis for risk
assessment by broadening the application of probabilistic exposure
techniques and PBPK models. The Agency has a conceptually similar
effort on-going to link PBPK models for pyrethroids with Stochastic
Human Exposure and Dose Simulator (SHEDS) exposure software, a
probabilistic exposure model developed by the EPA's Office of Research
and Development, which was reviewed by the SAP in July 2010. The
current effort by Dow AgroSciences is a research effort which may, if
sufficiently robust, inform future risk assessments; the February
meeting is a key milestone in this research. The Agency will solicit
feedback from the Panel on technical issues related to PBPK/PD model,
the proposed approach for merging the PBPK/PD model with CARES, and the
use of such merged models in risk assessment.
C. FIFRA SAP Documents and Meeting Minutes
EPA's background paper, related supporting materials, charge/
questions to FIFRA SAP, FIFRA SAP composition (i.e., members and ad hoc
members for this meeting), and the meeting agenda will be available by
late January 2011. 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.
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 Web site or may be
obtained from the OPP Regulatory Public Docket at https://www.regulations.gov.
List of Subjects
Environmental protection, Pesticides and pests.
Dated: November 23, 2010.
Frank Sanders,
Director, Office of Science Coordination and Policy.
[FR Doc. 2010-30630 Filed 12-7-10; 8:45 am]
BILLING CODE 6560-50-P