Interagency Coordinating Committee on the Validation of Alternative Methods Communities of Practice Webinar on Implementing Computational Approaches for Regulatory Safety Assessments; Notice of Public Webinar; Registration Information, 2963-2964 [2024-00758]
Download as PDF
Federal Register / Vol. 89, No. 11 / Wednesday, January 17, 2024 / Notices
guidelines may be formally referenced
as ‘‘the poverty guidelines updated
periodically in the Federal Register by
the U.S. Department of Health and
Human Services under the authority of
42 U.S.C. 9902(2).’’
Some federal programs use a
percentage multiple of the guidelines
(for example, 125 percent or 185 percent
of the guidelines), as noted in relevant
authorizing legislation or program
regulations. Non-Federal organizations
that use the poverty guidelines under
their own authority in non-federallyfunded activities also may choose to use
a percentage multiple of the guidelines.
The poverty guidelines do not make a
distinction between farm and non-farm
families, or between aged and non-aged
units. (Only the Census Bureau poverty
thresholds have separate figures for aged
and non-aged one-person and twoperson units.)
This notice does not provide
definitions of such terms as ‘‘income’’ or
‘‘family’’ as there is considerable
variation of these terms among programs
that use the poverty guidelines. The
legislation or regulations governing each
program define these terms and
determine how the program applies the
poverty guidelines. In cases where
legislation or regulations do not
establish these definitions, the entity
that administers or funds the program is
responsible to define such terms as
‘‘income’’ and ‘‘family.’’ Therefore,
questions such as net or gross income,
counted or excluded income, or
household size should be directed to the
entity that administers or funds the
program.
Dated: January 11, 2024.
Xavier Becerra,
Secretary, Department of Health and Human
Services.
[FR Doc. 2024–00796 Filed 1–16–24; 8:45 am]
BILLING CODE 4150–05–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
lotter on DSK11XQN23PROD with NOTICES1
National Institutes of Health
Interagency Coordinating Committee
on the Validation of Alternative
Methods Communities of Practice
Webinar on Implementing
Computational Approaches for
Regulatory Safety Assessments;
Notice of Public Webinar; Registration
Information
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
VerDate Sep<11>2014
18:14 Jan 16, 2024
Jkt 262001
The Interagency Coordinating
Committee on the Validation of
Alternative Methods (ICCVAM)
announces the public webinar
‘‘Implementing Computational
Approaches for Regulatory Safety
Assessments.’’ The webinar is organized
on behalf of ICCVAM by the National
Toxicology Program Interagency Center
for the Evaluation of Alternative
Toxicological Methods (NICEATM).
Interested persons may participate via
the web meeting platform. Time will be
allotted for questions from the audience.
Information about the webinar and
registration are available at https://
ntp.niehs.nih.gov/go/commprac-2024.
DATES:
Webinar: January 29, 2024, 10 a.m. to
approximately 12 noon EST.
Registration for Webinar: January 10,
2024, until 12:00 noon EST January 29,
2024. Registration to view the webinar
is required.
ADDRESSES: Webinar web page: https://
ntp.niehs.nih.gov/go/commprac-2024.
FOR FURTHER INFORMATION CONTACT: Dr.
Helena Hogberg, Staff Scientist,
NICEATM, email: helena.hogbergdurdock@nih.gov, telephone: (984) 287–
3150.
SUPPLEMENTARY INFORMATION:
Background: ICCVAM promotes the
development and validation of toxicity
testing methods that protect human
health and the environment while
replacing, reducing, or refining animal
use. ICCVAM also provides guidance to
test method developers and facilitates
collaborations that promote the
development of new test methods. To
address these goals, ICCVAM will hold
a Communities of Practice webinar on
‘‘Implementing Computational
Approaches for Regulatory Safety
Assessments.’’
Computational toxicology methods
can be useful for generating bioactivity
predictions for chemicals for which
limited toxicity data are available. They
can also help users understand and
interpret large, diverse bioactivity data
sets, or predict how a chemical might
behave in the body. However, users
with limited experience with such
methods may find it difficult to use
them or interpret their outputs, or even
understand how the methods could be
applied in a specific context.
This webinar will discuss how to
establish confidence in computational
approaches for regulatory applications.
Ongoing activities and key insights will
be described in three presentations by
speakers from the U.S. government and
the private sector focusing on
applications of tools such as structurebased models to predict chemical
SUMMARY:
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
2963
bioactivity and pharmacokinetic models
to support understanding of chemical
metabolism and disposition. The
preliminary agenda and additional
information about presentations will be
posted at https://ntp.niehs.nih.gov/go/
commprac-2024 as they become
available.
Webinar and Registration: This
webinar is open to the public with time
scheduled for questions by participants
following each presentation.
Registration for the webinar is required.
Registration will open on or before
January 10, 2024, and remain open
through 12 noon EST on January 29,
2024. Registration is available at https://
ntp.niehs.nih.gov/go/commprac-2024.
Interested individuals are encouraged to
visit this web page to stay abreast of the
most current webinar information.
Registrants will receive instructions on
how to access and participate in the
webinar in the email confirming their
registration. TTY users should contact
the Federal TTY Relay Service at 800–
877–8339. Requests should be made at
least five business days in advance of
the event.
Background Information on ICCVAM
and NICEATM: ICCVAM is an
interagency committee composed of
representatives from 17 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. ICCVAM also
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
animal use.
The ICCVAM Authorization Act of
2000 (42 U.S.C. 285l–3) establishes
ICCVAM as a permanent interagency
committee of the National Institute of
Environmental Health Sciences 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 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,
E:\FR\FM\17JAN1.SGM
17JAN1
2964
Federal Register / Vol. 89, No. 11 / Wednesday, January 17, 2024 / Notices
revised, and alternative test methods
and strategies for validation studies and
technical evaluations. Additional
information about NICEATM can be
found at https://ntp.niehs.nih.gov/go/
niceatm.
Dated: January 10, 2024.
Richard P. Woychik,
Director, National Institute of Environmental
Health Sciences and National Toxicology
Program, National Institutes of Health.
Dated: January 11, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–00794 Filed 1–16–24; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
[FR Doc. 2024–00758 Filed 1–16–24; 8:45 am]
National Cancer Institute; Notice of
Closed Meetings
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Neurological
Disorders and Stroke; Notice of Closed
Meeting
lotter on DSK11XQN23PROD with NOTICES1
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; NINDS R35 Overflow
Meeting.
Date: January 19, 2024.
Time: 11:00 a.m. to 1:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852.
Contact Person: DeAnna Lynn Adkins,
Ph.D., Scientific Review Officer, Scientific
Review Branch, Division of Extramural
Activities, NINDS/NIH NSC, 6001 Executive
Blvd., Rockville, MD 20852, 301–496–9223,
deanna.adkins@nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.853, Clinical Research
Related to Neurological Disorders; 93.854,
Biological Basis Research in the
Neurosciences, National Institutes of Health,
HHS.)
VerDate Sep<11>2014
18:14 Jan 16, 2024
Jkt 262001
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications/
contract proposals and the discussions
could disclose confidential trade secrets
or commercial property such as
patentable material, and personal
information concerning individuals
associated with the grant applications/
contract proposals, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: National Cancer
Institute Special Emphasis Panel TEP–8:
SBIR Contract Review.
Date: February 14, 2024.
Time: 11:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Cancer Institute, Shady
Grove, 9609 Medical Center Drive, Room
7W254, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Susan Lynn Spence, Ph.D.,
Scientific Review Officer, Research
Technology and Contract Review Branch,
Division of Extramural Activities, National
Cancer Institute, NIH, 9609 Medical Center
Drive, Room 7W254, Rockville, Maryland
20850, 240–620–0819, susan.spence@
nih.gov.
Name of Committee: National Cancer
Institute Special Emphasis Panel; TEP–6A:
SBIR Contract Review.
Date: February 22–23, 2024.
Time: 10:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Cancer Institute Shady
Grove, 9609 Medical Center Drive, Room
7W254, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Susan Lynn Spence, Ph.D.,
Scientific Review Officer, Research
Technology and Contract Review Branch,
Division of Extramural Activities, National
Cancer Institute, NIH, 9609 Medical Center
Drive, Room 7W254, Rockville, Maryland
20850, 240–620–0819, susan.spence@
nih.gov.
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
Name of Committee: National Cancer
Institute Special Emphasis Panel; Human
Tumor Atlas (HTA) Research Centers (U01).
Date: February 29, 2024.
Time: 9:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Cancer Institute at Shady
Grove, 9609 Medical Center Drive, Room
7W240, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Hasan Siddiqui, Ph.D.,
Scientific Review Officer, Special Review
Branch, Division of Extramural Activities,
National Cancer Institute, NIH, 9609 Medical
Center Drive, Room 7W240, Rockville,
Maryland 20850, 240–276–5122,
hasan.siddiqui@nih.gov.
Name of Committee: National Cancer
Institute Special Emphasis Panel; TEP–6B:
SBIR Contract Review.
Date: March 1, 2024.
Time: 11:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Cancer Institute Shady
Grove, 9609 Medical Center Drive, Room
7W254, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Susan Lynn Spence, Ph.D.,
Scientific Review Officer, Research
Technology and Contract Review Branch,
Division of Extramural Activities, National
Cancer Institute, NIH, 9609 Medical Center
Drive, Room 7W254, Rockville, Maryland
20850, 240–620–0819, susan.spence@
nih.gov.
Name of Committee: National Cancer
Institute Special Emphasis Panel; SEP 11:
NCI Clinical and Translational Cancer
Research.
Date: March 7, 2024.
Time: 11:00 a.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Cancer Institute at Shady
Grove, 9609 Medical Center Drive, Room
7W602, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Delia Tang, M.D.,
Scientific Review Officer, Resources and
Training Review Branch, Division of
Extramural Activities, National Cancer
Institute, NIH, 9609 Medical Center Drive,
Room 7W602, Rockville, Maryland 20850,
240–276–6456, tangd@mail.nih.gov.
Name of Committee: National Cancer
Institute Special Emphasis Panel;
Translational Research Toward Development
of a Kaposi Sarcoma Herpesvirus (KSHV)
Vaccine (U01).
Date: March 12, 2024.
Time: 10:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Cancer Institute at Shady
Grove, 9609 Medical Center Drive, Room
7W264, Rockville, Maryland 20850 (Virtual
Meeting).
Contact Person: Ombretta Salvucci, Ph.D.,
Scientific Review Officer, Special Review
Branch, Division of Extramural Activities,
National Cancer Institute, NIH, 9609 Medical
Center Drive, Room 7W264, Rockville,
Maryland 20850, 240–276–7286, salvucco@
mail.nih.gov.
E:\FR\FM\17JAN1.SGM
17JAN1
Agencies
[Federal Register Volume 89, Number 11 (Wednesday, January 17, 2024)]
[Notices]
[Pages 2963-2964]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-00758]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Interagency Coordinating Committee on the Validation of
Alternative Methods Communities of Practice Webinar on Implementing
Computational Approaches for Regulatory Safety Assessments; Notice of
Public Webinar; Registration Information
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Interagency Coordinating Committee on the Validation of
Alternative Methods (ICCVAM) announces the public webinar
``Implementing Computational Approaches for Regulatory Safety
Assessments.'' The webinar is organized on behalf of ICCVAM by the
National Toxicology Program Interagency Center for the Evaluation of
Alternative Toxicological Methods (NICEATM). Interested persons may
participate via the web meeting platform. Time will be allotted for
questions from the audience. Information about the webinar and
registration are available at https://ntp.niehs.nih.gov/go/commprac-2024.
DATES:
Webinar: January 29, 2024, 10 a.m. to approximately 12 noon EST.
Registration for Webinar: January 10, 2024, until 12:00 noon EST
January 29, 2024. Registration to view the webinar is required.
ADDRESSES: Webinar web page: https://ntp.niehs.nih.gov/go/commprac-2024.
FOR FURTHER INFORMATION CONTACT: Dr. Helena Hogberg, Staff Scientist,
NICEATM, email: [email protected], telephone: (984) 287-
3150.
SUPPLEMENTARY INFORMATION:
Background: ICCVAM promotes the development and validation of
toxicity testing methods that protect human health and the environment
while replacing, reducing, or refining animal use. ICCVAM also provides
guidance to test method developers and facilitates collaborations that
promote the development of new test methods. To address these goals,
ICCVAM will hold a Communities of Practice webinar on ``Implementing
Computational Approaches for Regulatory Safety Assessments.''
Computational toxicology methods can be useful for generating
bioactivity predictions for chemicals for which limited toxicity data
are available. They can also help users understand and interpret large,
diverse bioactivity data sets, or predict how a chemical might behave
in the body. However, users with limited experience with such methods
may find it difficult to use them or interpret their outputs, or even
understand how the methods could be applied in a specific context.
This webinar will discuss how to establish confidence in
computational approaches for regulatory applications. Ongoing
activities and key insights will be described in three presentations by
speakers from the U.S. government and the private sector focusing on
applications of tools such as structure-based models to predict
chemical bioactivity and pharmacokinetic models to support
understanding of chemical metabolism and disposition. The preliminary
agenda and additional information about presentations will be posted at
https://ntp.niehs.nih.gov/go/commprac-2024 as they become available.
Webinar and Registration: This webinar is open to the public with
time scheduled for questions by participants following each
presentation. Registration for the webinar is required. Registration
will open on or before January 10, 2024, and remain open through 12
noon EST on January 29, 2024. Registration is available at https://ntp.niehs.nih.gov/go/commprac-2024. Interested individuals are
encouraged to visit this web page to stay abreast of the most current
webinar information. Registrants will receive instructions on how to
access and participate in the webinar in the email confirming their
registration. TTY users should contact the Federal TTY Relay Service at
800-877-8339. Requests should be made at least five business days in
advance of the event.
Background Information on ICCVAM and NICEATM: ICCVAM is an
interagency committee composed of representatives from 17 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. ICCVAM also 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 animal use.
The ICCVAM Authorization Act of 2000 (42 U.S.C. 285l-3) establishes
ICCVAM as a permanent interagency committee of the National Institute
of Environmental Health Sciences 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 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,
[[Page 2964]]
revised, and alternative test methods and strategies for validation
studies and technical evaluations. Additional information about NICEATM
can be found at https://ntp.niehs.nih.gov/go/niceatm.
Dated: January 10, 2024.
Richard P. Woychik,
Director, National Institute of Environmental Health Sciences and
National Toxicology Program, National Institutes of Health.
[FR Doc. 2024-00758 Filed 1-16-24; 8:45 am]
BILLING CODE 4140-01-P