Advisory Committee; Science Advisory Board to the National Center for Toxicological Research; Termination; Removal From List of Standing Committees, 46802 [2024-11811]
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Federal Register / Vol. 89, No. 105 / Thursday, May 30, 2024 / Rules and Regulations
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[FR Doc. 2024–11792 Filed 5–29–24; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 14
[Docket No. FDA–2024–N–2357]
Advisory Committee; Science Advisory
Board to the National Center for
Toxicological Research; Termination;
Removal From List of Standing
Committees
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule.
The Food and Drug
Administration (FDA or Agency) is
announcing the termination of the
Science Advisory Board to the National
Center for Toxicological Research
(NCTR). This document announces the
reasons for termination and removes the
Science Advisory Board to the NCTR
from the Agency’s list of standing
advisory committees.
DATES: This rule is effective May 30,
2024.
ddrumheller on DSK120RN23PROD with RULES1
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Ashley Groves, Designated Federal
Officer, National Center for
Toxicological Research, Food and Drug
Administration, 3900 NCTR Rd., 50–
VerDate Sep<11>2014
15:52 May 29, 2024
Jkt 262001
719, Jefferson, AR 72079, 870–543–
7956, Ashley.Groves@fda.hhs.gov.
The
Science Advisory Board to the National
Center for Toxicological Research (the
Committee) was established on June 2,
1973 (38 FR 18478). The Committee
advises the Commissioner of Food and
Drugs or designee in discharging
responsibilities as they relate to helping
to ensure safe and effective drugs for
human use and as required, any other
product for which FDA has regulatory
responsibility.
The Committee is no longer needed
and will be terminated on June 2, 2024.
Over the past several years, the
Committee has met very infrequently,
and the effort and expense of
maintaining the Committee are no
longer justified. The Science Board to
FDA (Science Board) provides advice to
the Commissioner and other appropriate
officials on specific complex scientific
and technical issues important to FDA
and its mission, including emerging
issues within the scientific community.
Additionally, the Committee provides
advice that supports the Agency in
keeping pace with technical and
scientific developments, including in
regulatory science; and input into the
Agency’s research agenda; and on
upgrading its scientific and research
facilities and training opportunities. It
also provides, where requested, expert
review of Agency-sponsored intramural
and extramural scientific research
programs. In the future, any issues on
which NCTR requires expert advice will
be addressed by utilizing the Science
Board with additional augmentation of
expertise by appropriate subject matter
experts serving as temporary members
on that committee.
Under 5 U.S.C. 553(b)(3)(B) and (d)
and 21 CFR 10.40(d) and (e), the Agency
finds good cause to dispense with notice
and public comment procedures and to
proceed to an immediate effective date
on this rule.
Notice and public comment and a
delayed effective date are unnecessary
because the Committee is not being
adequately used, and termination of the
committee is effective on June 2, 2024,
in accordance with 21 CFR 14.55. This
final rule merely removes the name of
the Science Advisory Board to the
National Center for Toxicological
Research from the list of standing
advisory committees in § 14.100 (21
CFR 14.100).
Therefore, the Agency is amending
§ 14.100(e) as set forth in the regulatory
text of the document.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00006
Fmt 4700
Sfmt 4700
List of Subjects in 21 CFR Part 14
Administrative practice and
procedure, Advisory committee, Color
additives, Drugs, Radiation protection.
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs, 21 CFR part 14 is
amended as follows:
PART 14—PUBLIC HEARING BEFORE
A PUBLIC ADVISORY COMMITTEE
1. The authority citation for part 14
continues to read as follows:
■
Authority: 5 U.S.C. 1001 et seq.; 15 U.S.C.
1451–1461; 21 U.S.C. 41–50, 141–149, 321–
394, 467f, 679, 821, 1034; 28 U.S.C. 2112; 42
U.S.C. 201, 262, 263b, 264, 284m, 284m–1;
Pub. L. 107–109, 115 Stat. 1419.
§ 14.100
[Amended]
2. Amend § 14.100 by removing
paragraph (e).
■
Dated: May 23, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–11811 Filed 5–29–24; 8:45 am]
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Office of Foreign Assets Control
31 CFR Part 591
Publication of Venezuela Sanctions
Regulations Web General License 8N
Office of Foreign Assets
Control, Treasury.
ACTION: Publication of a Web General
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AGENCY:
The Department of the
Treasury’s Office of Foreign Assets
Control (OFAC) is publishing one
general license (GL) issued pursuant to
the Venezuela Sanctions Regulations:
GL 8N, which was previously made
available on OFAC’s website.
DATES: GL 8N was issued on May 10,
2024. See SUPPLEMENTARY INFORMATION
for additional relevant dates.
FOR FURTHER INFORMATION CONTACT:
OFAC: Assistant Director for Licensing,
202–622–2480; Assistant Director for
Regulatory Affairs, 202–622–4855; or
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SUMMARY:
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E:\FR\FM\30MYR1.SGM
30MYR1
Agencies
[Federal Register Volume 89, Number 105 (Thursday, May 30, 2024)]
[Rules and Regulations]
[Page 46802]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-11811]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 14
[Docket No. FDA-2024-N-2357]
Advisory Committee; Science Advisory Board to the National Center
for Toxicological Research; Termination; Removal From List of Standing
Committees
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or Agency) is announcing
the termination of the Science Advisory Board to the National Center
for Toxicological Research (NCTR). This document announces the reasons
for termination and removes the Science Advisory Board to the NCTR from
the Agency's list of standing advisory committees.
DATES: This rule is effective May 30, 2024.
FOR FURTHER INFORMATION CONTACT: Ashley Groves, Designated Federal
Officer, National Center for Toxicological Research, Food and Drug
Administration, 3900 NCTR Rd., 50-719, Jefferson, AR 72079, 870-543-
7956, [email protected].
SUPPLEMENTARY INFORMATION: The Science Advisory Board to the National
Center for Toxicological Research (the Committee) was established on
June 2, 1973 (38 FR 18478). The Committee advises the Commissioner of
Food and Drugs or designee in discharging responsibilities as they
relate to helping to ensure safe and effective drugs for human use and
as required, any other product for which FDA has regulatory
responsibility.
The Committee is no longer needed and will be terminated on June 2,
2024. Over the past several years, the Committee has met very
infrequently, and the effort and expense of maintaining the Committee
are no longer justified. The Science Board to FDA (Science Board)
provides advice to the Commissioner and other appropriate officials on
specific complex scientific and technical issues important to FDA and
its mission, including emerging issues within the scientific community.
Additionally, the Committee provides advice that supports the Agency in
keeping pace with technical and scientific developments, including in
regulatory science; and input into the Agency's research agenda; and on
upgrading its scientific and research facilities and training
opportunities. It also provides, where requested, expert review of
Agency-sponsored intramural and extramural scientific research
programs. In the future, any issues on which NCTR requires expert
advice will be addressed by utilizing the Science Board with additional
augmentation of expertise by appropriate subject matter experts serving
as temporary members on that committee.
Under 5 U.S.C. 553(b)(3)(B) and (d) and 21 CFR 10.40(d) and (e),
the Agency finds good cause to dispense with notice and public comment
procedures and to proceed to an immediate effective date on this rule.
Notice and public comment and a delayed effective date are
unnecessary because the Committee is not being adequately used, and
termination of the committee is effective on June 2, 2024, in
accordance with 21 CFR 14.55. This final rule merely removes the name
of the Science Advisory Board to the National Center for Toxicological
Research from the list of standing advisory committees in Sec. 14.100
(21 CFR 14.100).
Therefore, the Agency is amending Sec. 14.100(e) as set forth in
the regulatory text of the document.
List of Subjects in 21 CFR Part 14
Administrative practice and procedure, Advisory committee, Color
additives, Drugs, Radiation protection.
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs, 21 CFR part
14 is amended as follows:
PART 14--PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
0
1. The authority citation for part 14 continues to read as follows:
Authority: 5 U.S.C. 1001 et seq.; 15 U.S.C. 1451-1461; 21 U.S.C.
41-50, 141-149, 321-394, 467f, 679, 821, 1034; 28 U.S.C. 2112; 42
U.S.C. 201, 262, 263b, 264, 284m, 284m-1; Pub. L. 107-109, 115 Stat.
1419.
Sec. 14.100 [Amended]
0
2. Amend Sec. 14.100 by removing paragraph (e).
Dated: May 23, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024-11811 Filed 5-29-24; 8:45 am]
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