Interagency Coordinating Committee on the Validation of Alternative Methods Biennial Progress Report: 2018-2019; Availability of Report, 43249-43250 [2020-15341]
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Committee Policy.
[FR Doc. 2020–15379 Filed 7–15–20; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Interagency Coordinating Committee
on the Validation of Alternative
Methods Biennial Progress Report:
2018–2019; Availability of Report
National Institutes of Health,
Health and Human Services (HHS).
ACTION: Notice.
AGENCY:
The National Toxicology
Program (NTP) Interagency Center for
the Evaluation of Alternative
Toxicological Methods (NICEATM)
announces availability of the
Interagency Coordinating Committee on
the Validation of Alternative Methods
(ICCVAM) Biennial Progress Report:
2018–2019. This report, prepared in
accordance with requirements of the
ICCVAM Authorization Act of 2000,
describes activities and
accomplishments from January 2018
through December 2019.
ADDRESSES: The report is available at
https://ntp.niehs.nih.gov/iccvamreport/
2019/.
SUMMARY:
VerDate Sep<11>2014
17:43 Jul 15, 2020
Jkt 250001
Dr.
Nicole Kleinstreuer, Acting Director,
NICEATM, Division of NTP, NIEHS,
P.O. Box 12233, K2–17, Research
Triangle Park, NC 27709. Phone: 984–
287–3150, Email: nicole.kleinstreuer@
nih.gov. Hand Deliver/Courier address:
530 Davis Drive, Room K2032,
Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
Background: The ICCVAM
Authorization Act of 2000 (42 U.S.C.
285l-3), established ICCVAM as a
permanent interagency committee of the
National Institute of Environmental
Health Sciences (NIEHS) under
NICEATM. ICCVAM’s mission is to
facilitate development, validation, and
regulatory acceptance of new and
revised regulatory test methods that
reduce, refine, or replace the use of
animals in testing while maintaining
and promoting scientific quality and the
protection of human health, animal
health, and the environment.
A provision of the ICCVAM
Authorization Act states that ICCVAM
shall prepare ‘‘reports to be made
available to the public on its progress
under this Act.’’ The tenth ICCVAM
biennial progress report describing
ICCVAM activities and
accomplishments from January 2018
through December 2019 is now
available.
Summary of Report Contents: Key
ICCVAM, ICCVAM agency, and
NICEATM accomplishments
summarized in the report include:
• Publication in January 2018 of a
strategic roadmap for incorporating new
approaches into safety testing of
chemicals and medical products in the
United States, and progress toward goals
described in the strategic roadmap.
• Development of the Collaborative
Acute Toxicity Modeling Suite, an
online resource for screening organic
chemicals for acute oral toxicity, and
expansion of NICEATM’s Integrated
Chemical Environment, which provides
curated data and tools for safety
assessment of chemicals.
• Initiatives by the U.S.
Environmental Protection Agency to
reduce animal use: A draft science
policy to reduce animal use for skin
sensitization testing for pesticide
registration, a plan to reduce vertebrate
animal testing for chemical safety
information required under the Toxic
Substances Control Act, and an agencywide directive to reduce mammal study
requests and funding 30% by 2025 and
completely eliminating them by 2035.
• Development of a strategic roadmap
by the Department of Defense to help its
laboratories better define their chemical
FOR FURTHER INFORMATION CONTACT:
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43249
assessment needs and collaborate on
development or refinement of
appropriate non-animal approaches for
testing.
• Implementation by the U.S. Food
and Drug Administration of its
predictive toxicity roadmap for
integrating predictive toxicology
methods into safety and risk
assessments.
Availability of Report: The report is
available at https://ntp.niehs.nih.gov/
iccvamreport/2019/. Links to
this report and all past ICCVAM annual
and biennial reports are available at
https://ntp.niehs.nih.gov/go/iccvam-bien.
Background Information on ICCVAM
and NICEATM: ICCVAM is an
interagency committee composed of
representatives from 16 federal
regulatory and research agencies that
require, use, generate, or disseminate
toxicological and safety testing
information. ICCVAM conducts
technical evaluations of new, revised,
and alternative safety testing methods
and integrated testing strategies with
regulatory applicability and promotes
the scientific validation and regulatory
acceptance of testing methods that more
accurately assess the safety and hazards
of chemicals and products and replace,
reduce, or refine (enhance animal wellbeing and lessen or avoid pain and
distress) animal use.
The ICCVAM Authorization Act of
2000 (42 U.S.C. 285l–3) establishes
ICCVAM as a permanent interagency
committee of NIEHS and provides the
authority for ICCVAM involvement in
activities relevant to the development of
alternative test methods. Additional
information about ICCVAM can be
found at https://ntp.niehs.nih.gov/go/
iccvam.
NICEATM administers ICCVAM,
provides scientific and operational
support for ICCVAM-related activities,
and conducts and publishes analyses
and evaluations of data from new,
revised, and alternative testing
approaches. NICEATM and ICCVAM
work collaboratively to evaluate new
and improved testing approaches
applicable to the needs of U.S. Federal
agencies. NICEATM and ICCVAM
welcome the public nomination of new,
revised, and alternative testing
approaches for validation studies and
technical evaluations. Additional
information about NICEATM can be
found at https://ntp.niehs.nih.gov/go/
niceatm.
E:\FR\FM\16JYN1.SGM
16JYN1
43250
Federal Register / Vol. 85, No. 137 / Thursday, July 16, 2020 / Notices
Dated: July 7, 2020.
Brian R. Berridge,
Associate Director, National Toxicology
Program.
Dated: July 13, 2020.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2020–15341 Filed 7–15–20; 8:45 am]
[FR Doc. 2020–15377 Filed 7–15–20; 8:45 am]
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17:43 Jul 15, 2020
Jkt 250001
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Agencies
[Federal Register Volume 85, Number 137 (Thursday, July 16, 2020)]
[Notices]
[Pages 43249-43250]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-15341]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Interagency Coordinating Committee on the Validation of
Alternative Methods Biennial Progress Report: 2018-2019; Availability
of Report
AGENCY: National Institutes of Health, Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The National Toxicology Program (NTP) Interagency Center for
the Evaluation of Alternative Toxicological Methods (NICEATM) announces
availability of the Interagency Coordinating Committee on the
Validation of Alternative Methods (ICCVAM) Biennial Progress Report:
2018-2019. This report, prepared in accordance with requirements of the
ICCVAM Authorization Act of 2000, describes activities and
accomplishments from January 2018 through December 2019.
ADDRESSES: The report is available at https://ntp.niehs.nih.gov/iccvamreport/2019/.
FOR FURTHER INFORMATION CONTACT: Dr. Nicole Kleinstreuer, Acting
Director, NICEATM, Division of NTP, NIEHS, P.O. Box 12233, K2-17,
Research Triangle Park, NC 27709. Phone: 984-287-3150, Email:
[email protected]. Hand Deliver/Courier address: 530 Davis
Drive, Room K2032, Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
Background: The ICCVAM Authorization Act of 2000 (42 U.S.C. 285l-
3), established ICCVAM as a permanent interagency committee of the
National Institute of Environmental Health Sciences (NIEHS) under
NICEATM. ICCVAM's mission is to facilitate development, validation, and
regulatory acceptance of new and revised regulatory test methods that
reduce, refine, or replace the use of animals in testing while
maintaining and promoting scientific quality and the protection of
human health, animal health, and the environment.
A provision of the ICCVAM Authorization Act states that ICCVAM
shall prepare ``reports to be made available to the public on its
progress under this Act.'' The tenth ICCVAM biennial progress report
describing ICCVAM activities and accomplishments from January 2018
through December 2019 is now available.
Summary of Report Contents: Key ICCVAM, ICCVAM agency, and NICEATM
accomplishments summarized in the report include:
Publication in January 2018 of a strategic roadmap for
incorporating new approaches into safety testing of chemicals and
medical products in the United States, and progress toward goals
described in the strategic roadmap.
Development of the Collaborative Acute Toxicity Modeling
Suite, an online resource for screening organic chemicals for acute
oral toxicity, and expansion of NICEATM's Integrated Chemical
Environment, which provides curated data and tools for safety
assessment of chemicals.
Initiatives by the U.S. Environmental Protection Agency to
reduce animal use: A draft science policy to reduce animal use for skin
sensitization testing for pesticide registration, a plan to reduce
vertebrate animal testing for chemical safety information required
under the Toxic Substances Control Act, and an agency-wide directive to
reduce mammal study requests and funding 30% by 2025 and completely
eliminating them by 2035.
Development of a strategic roadmap by the Department of
Defense to help its laboratories better define their chemical
assessment needs and collaborate on development or refinement of
appropriate non-animal approaches for testing.
Implementation by the U.S. Food and Drug Administration of
its predictive toxicity roadmap for integrating predictive toxicology
methods into safety and risk assessments.
Availability of Report: The report is available at https://ntp.niehs.nih.gov/iccvamreport/2019/. Links to this report
and all past ICCVAM annual and biennial reports are available at https://ntp.niehs.nih.gov/go/iccvam-bien.
Background Information on ICCVAM and NICEATM: ICCVAM is an
interagency committee composed of representatives from 16 federal
regulatory and research agencies that require, use, generate, or
disseminate toxicological and safety testing information. ICCVAM
conducts technical evaluations of new, revised, and alternative safety
testing methods and integrated testing strategies with regulatory
applicability and promotes the scientific validation and regulatory
acceptance of testing methods that more accurately assess the safety
and hazards of chemicals and products and replace, reduce, or refine
(enhance animal well-being and lessen or avoid pain and distress)
animal use.
The ICCVAM Authorization Act of 2000 (42 U.S.C. 285l-3) establishes
ICCVAM as a permanent interagency committee of NIEHS and provides the
authority for ICCVAM involvement in activities relevant to the
development of alternative test methods. Additional information about
ICCVAM can be found at https://ntp.niehs.nih.gov/go/iccvam.
NICEATM administers ICCVAM, provides scientific and operational
support for ICCVAM-related activities, and conducts and publishes
analyses and evaluations of data from new, revised, and alternative
testing approaches. NICEATM and ICCVAM work collaboratively to evaluate
new and improved testing approaches applicable to the needs of U.S.
Federal agencies. NICEATM and ICCVAM welcome the public nomination of
new, revised, and alternative testing approaches for validation studies
and technical evaluations. Additional information about NICEATM can be
found at https://ntp.niehs.nih.gov/go/niceatm.
[[Page 43250]]
Dated: July 7, 2020.
Brian R. Berridge,
Associate Director, National Toxicology Program.
[FR Doc. 2020-15341 Filed 7-15-20; 8:45 am]
BILLING CODE 4140-01-P