National Toxicology Program; National Toxicology Program (NTP) Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM); Request for Data on Non-Animal Methods and Approaches for Determining Skin and Eye Irritation Potential of Antimicrobial Cleaning Product Formulations; Request for Nominations for an Independent Expert Panel, 13512-13513 [05-5471]
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13512
Federal Register / Vol. 70, No. 53 / Monday, March 21, 2005 / Notices
Dated: March 11, 2005.
Cassandra Isom,
Program Administrator, Office of Science
Education, National Institutes of Health.
[FR Doc. 05–5472 Filed 3–18–05; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program; National
Toxicology Program (NTP) Interagency
Center for the Evaluation of Alternative
Toxicological Methods (NICEATM);
Request for Data on Non-Animal
Methods and Approaches for
Determining Skin and Eye Irritation
Potential of Antimicrobial Cleaning
Product Formulations; Request for
Nominations for an Independent
Expert Panel
National Institute of
Environmental Health Sciences
(NIEHS), National Institutes of Health
(NIH).
ACTION: Request for data and nomination
of panelists.
AGENCY:
SUMMARY: The Interagency Coordinating
Committee on the Validation of
Alternative Methods (ICCVAM) and
NICEATM are requesting the
submission of data that would assist in
evaluating the validation status of nonanimal methods and approaches used
for determining the skin and eye
irritation potential of antimicrobial
cleaning product formulations to meet
regulatory hazard classification and
labeling purposes. Additionally,
NICEATM is also requesting the
nomination of scientists for
consideration as potential members of
an independent scientific expert panel
(‘‘Panel’’) to evaluate the proposed
methods and approaches. The ICCVAM
will consider the conclusions and
recommendations from the Panel in
developing its recommendations on the
validation status of these methods.
DATES: Nominations and data should be
received by noon on May 5, 2005.
ADDRESSES: Nominations and data
should be sent by mail, fax, or email to
Dr. William S. Stokes, Director of
NICEATM at NICEATM, NIEHS, P.O.
Box 12233, MD EC–17, Research
Triangle Park, NC, 27709, (phone) 919–
541–2384, (fax) 919–541–0947, (e-mail)
niceatm@niehs.nih.gov. Courier address:
NICEATM, 79 T.W. Alexander Drive,
Building 4401, Room 3128, Research
Triangle Park, NC 27709.
FOR FURTHER INFORMATION CONTACT: Dr.
William S. Stokes, Director of
VerDate jul<14>2003
18:36 Mar 18, 2005
Jkt 205001
NICEATM, (phone) 919–541–2384, (fax)
919–541–0947, (email)
niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
In June 2004, the Environmental
Protection Agency (EPA) asked ICCVAM
to evaluate the validation status of
proposed non-animal approaches for
determining the skin and eye irritation
potential of antimicrobial cleaning
product formulations for meeting
regulatory hazard classification and
labeling requirements. ICCVAM
considered the EPA’s request and
recommended that the evaluation of
these non-animal approaches proceed as
a high priority. ICCVAM agreed to work
with the EPA and representatives of its
Pesticide Program Dialogue Committee
(PPDC) to help assure that the
submission provided to ICCVAM
contains all relevant information, data,
and appropriate analyses as described in
the ‘‘ICCVAM Guidelines for the
Nomination and Submission of New,
Revised, and Alternative Test Methods’’
(NIH publication 03–4508). The
NICEATM on behalf of ICCVAM plans
to convene an independent scientific
expert panel to review the submission,
develop conclusions on the validation
status of these methods, and make
recommendations about the usefulness
and limitations of these methods for
their intended purpose. The date for the
expert panel meeting has not been
determined but will be announced in a
future Federal Register notice.
Request for Data
Data, the nomination of experts, and
other information submitted in response
to this notice should be sent to
NICEATM at the address given above.
Data received by the deadline will be
made available on the ICCVAM/
NICEATM Web site at https://
iccvam.niehs.nih.gov and considered by
the Panel and ICCVAM.
When submitting data or information
on protocols, please reference this
Federal Register notice and provide
appropriate contact information (name,
affiliation, mailing address, phone, fax,
e-mail, and sponsoring organization, as
applicable). NICEATM prefers the
submission of raw untransformed data
in addition to any summary data
including the submission of copies of
pages from applicable study notebooks
and/or study reports, if available. In vivo
and in vitro data for each substance are
preferred. Post-marketing surveillance
data, ethical human studies, and
accidental exposure reports also are
sought when available and applicable.
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
Each submission for a chemical or
product should preferably include the
following information when available:
• Common and trade name.
• Chemical Abstracts Service Registry
Number (CASRN) for each ingredient of
a formulation, and the percent
composition of each ingredient.
• Chemical structure.
• Chemical class.
• Product class.
• Commercial source.
• Test protocol used for either in vivo
or in vitro testing.
• The extent to which the study
complies with national/international
Good Laboratory Practice (GLP)
guidelines.
• Date and testing organization.
Request for the Nomination of
Scientists for the Expert Panel
NICEATM invites the nomination of
scientists with relevant knowledge and
experience that can serve on the Panel
to evaluate in vitro dermal and ocular
toxicity test methods. Areas of relevant
expertise include, but are not limited to:
human and animal dermatotoxicology/
ophthalmology with an emphasis on
evaluation and treatment of chemical
injuries, in vivo dermal/ocular toxicity
testing, in vitro dermal/ocular
toxicology, test method validation, and
biostatistics. Each nomination should
include the person’s name, affiliation,
contact information (i.e., mailing
address, e-mail address, telephone and
fax numbers), a brief summary of
relevant experience and qualifications,
and curriculum vitae, if possible.
NICEATM and ICCVAM will also
consider nominations previously
submitted in response to a request for
scientific experts for the evaluation of in
vitro ocular test methods (Federal
Register, Vol. 69, No. 57, pp. 13859–
13861, March 24, 2004, available at
https://iccvam.niehs.nih.gov/) and do not
need to be resubmitted.
Background Information on ICCVAM
and NICEATM
ICCVAM is an interagency committee
composed of representatives from 15
Federal regulatory and research agencies
that use or generate toxicological
information. ICCVAM conducts
technical evaluations of new, revised,
and alternative methods with regulatory
applicability and promotes the scientific
validation and regulatory acceptance of
toxicological test methods that more
accurately assess the safety and hazards
of chemicals and products and that
refine, reduce, or replace animal use.
The ICCVAM Authorization Act of 2000
(Pub. L. 106–545, available at https://
iccvam.niehs.nih.gov/about/
E:\FR\FM\21MRN1.SGM
21MRN1
Federal Register / Vol. 70, No. 53 / Monday, March 21, 2005 / Notices
PL106545.htm) establishes ICCVAM as a
permanent interagency committee of the
NIEHS under the NICEATM. NICEATM
administers the ICCVAM and provides
scientific and operational support for
ICCVAM-related activities. NICEATM
and ICCVAM work collaboratively to
evaluate new and improved test
methods applicable to the needs of
Federal agencies. Additional
information about ICCVAM and
NICEATM can be found at the following
Web site: https://iccvam.niehs.nih.gov.
NIEHS, P. O. Box 12233, MD EC–17,
Research Triangle Park, NC 27709,
(phone) 919–541–2384, (fax) 919–541–
0947, (e-mail) niceatm@niehs.nih.gov.
Courier address: NICEATM, 79 T.W.
Alexander Drive, Building 4401, Room
3128, Research Triangle Park, NC 27709.
FOR FURTHER INFORMATION CONTACT: Dr.
William S. Stokes, Director of
NICEATM, (phone) 919–541–2384, (email) niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Dated: March 9, 2005.
Samuel Wilson,
Deputy Director, National Institute of
Environmental Health Sciences.
[FR Doc. 05–5471 Filed 3–18–05; 8:45 am]
Background
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program; National
Toxicology Program (NTP) Interagency
Center for the Evaluation of Alternative
Toxicological Methods (NICEATM);
Availability of Expert Panel Report on
the Evaluation of the Current
Validation Status of In Vitro Test
Methods for Identifying Ocular
Corrosives and Severe Irritants
National Institute of
Environmental Health Sciences
(NIEHS), National Institutes of Health
(NIH).
ACTION: Availability of report and
request for comments.
AGENCY:
The National Toxicology
Program (NTP) Interagency Center for
the Evaluation of Alternative
Toxicological Methods (NICEATM)
announces the availability of a report
entitled, ‘‘The Interagency Coordinating
Committee on the Validation of
Alternative Methods (ICCVAM) Expert
Panel Evaluation of the Current
Validation Status of In Vitro Test
Methods for Identifying Ocular
Corrosives and Severe Irritants.’’ The
NICEATM invites public comment on
the expert panel report. Copies of the
expert panel report may be obtained on
the ICCVAM/NICEATM Web site at
https://iccvam.niehs.nih.gov, or by
contacting NICEATM at the address
given below.
DATES: Written comments and
additional information should be
received by noon on May 5, 2005.
ADDRESSES: Comments and additional
information should be sent by mail, fax,
or e-mail to Dr. William S. Stokes,
Director of NICEATM, at NICEATM,
SUMMARY:
VerDate jul<14>2003
18:36 Mar 18, 2005
Jkt 205001
On January 11 and 12, 2005,
NICEATM and ICCVAM held an expert
panel meeting to evaluate the validation
status for four in vitro ocular test
methods nominated by the EPA: (1) The
Bovine Corneal Opacity and
Permeability (BCOP) test; (2) the Hen’s
Egg Test—Chorion Allantoic Membrane
(HET–CAM); (3) the Isolated Rabbit Eye
(IRE) test; and (4) the Isolated Chicken
Eye (ICE) test. At this meeting, the
expert panel reviewed the Background
Review Document (BRD) for each
method and was asked to:
• Evaluate the extent and adequacy
that each method’s BRD addresses the
applicable ICCVAM validation and
acceptance criteria based on available
information and data, or will address
the criteria in proposed studies, focused
on identifying ocular corrosives and
severe irritants in a tiered testing
strategy.
• Develop conclusions and
recommendations on:
—The current usefulness and
limitations of each of the four test
methods for identifying ocular
corrosives and severe/irreversible
irritants.
—The test method protocol that should
be used for future testing and
validation studies.
—The adequacy of proposed
optimization and/or validation
studies.
—The adequacy of reference substances
proposed for future validation studies.
The expert panel’s conclusions and
recommendations on the four test
methods are described in ‘‘The ICCVAM
Expert Panel Evaluation of the Current
Validation Status of In Vitro Test
Methods for Identifying Ocular
Corrosives and Severe Irritants’’.
Prior to the expert panel meeting,
NICEATM issued several Federal
Register notices to (1) request public
comment on the EPA nomination of
ocular toxicity test methods and related
activities and request data on chemicals
evaluated by in vitro or in vivo ocular
irritancy test methods (Federal Register,
Vol. 69, No. 57, pp. 13859–13861,
PO 00000
Frm 00071
Fmt 4703
Sfmt 4703
13513
March 24, 2004, available at https://
iccvam.niehs.nih.gov/); (2) request the
nomination of scientific experts to serve
on the expert panel (Federal Register,
Vol. 69, No. 77, pg. 21565, April 21,
2004, available at https://
iccvam.niehs.nih.gov/); and (3) request
public comments on the BRDs prepared
by NICEATM for each of the four test
methods (Federal Register, Vol. 69, No.
212, pp. 64081–64082, November 3,
2004, and public comments are
available at
https://iccvam.niehs.nih.gov/).
Request for Comments
NICEATM invites the submission of
written comments on the expert panel
report. When submitting written
comments please include appropriate
contact information (name, affiliation,
mailing address, phone, fax, email and
sponsoring organization, if applicable).
All written comments received by the
deadline listed above will be posted on
the ICCVAM/NICEATM Web site and
made available to ICCVAM.
ICCVAM will consider the expert
panel report and any written public
comments received on that report as it
prepares final ICCVAM test method
recommendations for the four in vitro
ocular test methods. An ICCVAM test
method evaluation report, which
includes the ICCVAM
recommendations, will be forwarded to
appropriate Federal agencies for their
consideration. This report also will be
available to the public on the ICCVAM/
NICEATM Web site and by request to
NICEATM.
Background Information on ICCVAM
and NICEATM
ICCVAM is an interagency committee
composed of representatives from 15
Federal regulatory and research agencies
that use or generate toxicological
information. ICCVAM conducts
technical evaluations of new, revised,
and alternative methods with regulatory
applicability, and promotes the
scientific validation and regulatory
acceptance of toxicological test methods
that more accurately assess the safety
and hazards of chemicals and products
and that refine, reduce, and replace
animal use. The ICCVAM Authorization
Act of 2000 (Pub. L. 106–545, available
at https://iccvam.niehs.nih.gov/about/
PL106545.htm) establishes ICCVAM as a
permanent interagency committee of the
NIEHS under the NICEATM. NICEATM
administers the ICCVAM and provides
scientific and operational support for
ICCVAM-related activities. NICEATM
and ICCVAM work collaboratively to
evaluate new and improved test
methods applicable to the needs of
E:\FR\FM\21MRN1.SGM
21MRN1
Agencies
[Federal Register Volume 70, Number 53 (Monday, March 21, 2005)]
[Notices]
[Pages 13512-13513]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-5471]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Toxicology Program; National Toxicology Program (NTP)
Interagency Center for the Evaluation of Alternative Toxicological
Methods (NICEATM); Request for Data on Non-Animal Methods and
Approaches for Determining Skin and Eye Irritation Potential of
Antimicrobial Cleaning Product Formulations; Request for Nominations
for an Independent Expert Panel
AGENCY: National Institute of Environmental Health Sciences (NIEHS),
National Institutes of Health (NIH).
ACTION: Request for data and nomination of panelists.
-----------------------------------------------------------------------
SUMMARY: The Interagency Coordinating Committee on the Validation of
Alternative Methods (ICCVAM) and NICEATM are requesting the submission
of data that would assist in evaluating the validation status of non-
animal methods and approaches used for determining the skin and eye
irritation potential of antimicrobial cleaning product formulations to
meet regulatory hazard classification and labeling purposes.
Additionally, NICEATM is also requesting the nomination of scientists
for consideration as potential members of an independent scientific
expert panel (``Panel'') to evaluate the proposed methods and
approaches. The ICCVAM will consider the conclusions and
recommendations from the Panel in developing its recommendations on the
validation status of these methods.
DATES: Nominations and data should be received by noon on May 5, 2005.
ADDRESSES: Nominations and data should be sent by mail, fax, or email
to Dr. William S. Stokes, Director of NICEATM at NICEATM, NIEHS, P.O.
Box 12233, MD EC-17, Research Triangle Park, NC, 27709, (phone) 919-
541-2384, (fax) 919-541-0947, (e-mail) niceatm@niehs.nih.gov. Courier
address: NICEATM, 79 T.W. Alexander Drive, Building 4401, Room 3128,
Research Triangle Park, NC 27709.
FOR FURTHER INFORMATION CONTACT: Dr. William S. Stokes, Director of
NICEATM, (phone) 919-541-2384, (fax) 919-541-0947, (email)
niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
In June 2004, the Environmental Protection Agency (EPA) asked
ICCVAM to evaluate the validation status of proposed non-animal
approaches for determining the skin and eye irritation potential of
antimicrobial cleaning product formulations for meeting regulatory
hazard classification and labeling requirements. ICCVAM considered the
EPA's request and recommended that the evaluation of these non-animal
approaches proceed as a high priority. ICCVAM agreed to work with the
EPA and representatives of its Pesticide Program Dialogue Committee
(PPDC) to help assure that the submission provided to ICCVAM contains
all relevant information, data, and appropriate analyses as described
in the ``ICCVAM Guidelines for the Nomination and Submission of New,
Revised, and Alternative Test Methods'' (NIH publication 03-4508). The
NICEATM on behalf of ICCVAM plans to convene an independent scientific
expert panel to review the submission, develop conclusions on the
validation status of these methods, and make recommendations about the
usefulness and limitations of these methods for their intended purpose.
The date for the expert panel meeting has not been determined but will
be announced in a future Federal Register notice.
Request for Data
Data, the nomination of experts, and other information submitted in
response to this notice should be sent to NICEATM at the address given
above. Data received by the deadline will be made available on the
ICCVAM/NICEATM Web site at https://iccvam.niehs.nih.gov and considered
by the Panel and ICCVAM.
When submitting data or information on protocols, please reference
this Federal Register notice and provide appropriate contact
information (name, affiliation, mailing address, phone, fax, e-mail,
and sponsoring organization, as applicable). NICEATM prefers the
submission of raw untransformed data in addition to any summary data
including the submission of copies of pages from applicable study
notebooks and/or study reports, if available. In vivo and in vitro data
for each substance are preferred. Post-marketing surveillance data,
ethical human studies, and accidental exposure reports also are sought
when available and applicable. Each submission for a chemical or
product should preferably include the following information when
available:
Common and trade name.
Chemical Abstracts Service Registry Number (CASRN) for
each ingredient of a formulation, and the percent composition of each
ingredient.
Chemical structure.
Chemical class.
Product class.
Commercial source.
Test protocol used for either in vivo or in vitro testing.
The extent to which the study complies with national/
international Good Laboratory Practice (GLP) guidelines.
Date and testing organization.
Request for the Nomination of Scientists for the Expert Panel
NICEATM invites the nomination of scientists with relevant
knowledge and experience that can serve on the Panel to evaluate in
vitro dermal and ocular toxicity test methods. Areas of relevant
expertise include, but are not limited to: human and animal
dermatotoxicology/ophthalmology with an emphasis on evaluation and
treatment of chemical injuries, in vivo dermal/ocular toxicity testing,
in vitro dermal/ocular toxicology, test method validation, and
biostatistics. Each nomination should include the person's name,
affiliation, contact information (i.e., mailing address, e-mail
address, telephone and fax numbers), a brief summary of relevant
experience and qualifications, and curriculum vitae, if possible.
NICEATM and ICCVAM will also consider nominations previously submitted
in response to a request for scientific experts for the evaluation of
in vitro ocular test methods (Federal Register, Vol. 69, No. 57, pp.
13859-13861, March 24, 2004, available at https://iccvam.niehs.nih.gov/)
and do not need to be resubmitted.
Background Information on ICCVAM and NICEATM
ICCVAM is an interagency committee composed of representatives from
15 Federal regulatory and research agencies that use or generate
toxicological information. ICCVAM conducts technical evaluations of
new, revised, and alternative methods with regulatory applicability and
promotes the scientific validation and regulatory acceptance of
toxicological test methods that more accurately assess the safety and
hazards of chemicals and products and that refine, reduce, or replace
animal use. The ICCVAM Authorization Act of 2000 (Pub. L. 106-545,
available at https://iccvam.niehs.nih.gov/about/
[[Page 13513]]
PL106545.htm) establishes ICCVAM as a permanent interagency committee
of the NIEHS under the NICEATM. NICEATM administers the ICCVAM and
provides scientific and operational support for ICCVAM-related
activities. NICEATM and ICCVAM work collaboratively to evaluate new and
improved test methods applicable to the needs of Federal agencies.
Additional information about ICCVAM and NICEATM can be found at the
following Web site: https://iccvam.niehs.nih.gov.
Dated: March 9, 2005.
Samuel Wilson,
Deputy Director, National Institute of Environmental Health Sciences.
[FR Doc. 05-5471 Filed 3-18-05; 8:45 am]
BILLING CODE 4140-01-P