Advisory Committee; Science Advisory Board to the National Center for Toxicological Research; Termination; Removal From List of Standing Committees, 46802 [2024-11811]

Download as PDF 46802 Federal Register / Vol. 89, No. 105 / Thursday, May 30, 2024 / Rules and Regulations Cradle Swings, approved on February 1, 2024. The Director of the Federal Register approves this incorporation by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. You may inspect a copy at the Office of the Secretary, U.S. Consumer Product Safety Commission, 4330 East West Highway, Bethesda, MD 20814, telephone (301) 504–7479, email cpscos@cpsc.gov, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, email fr.inspection@nara.gov, or go to: www.archives.gov/federal-register/cfr/ ibr-locations. A read-only copy of the standard is available for viewing on the ASTM website at https://www.astm.org/ READINGLIBRARY/. You may obtain a copy from ASTM International, 100 Barr Harbor Drive, P.O. Box C700, West Conshohocken, PA 19428–2959; telephone (610) 832–9500; www.astm.org. Alberta E. Mills, Secretary, Consumer Product Safety Commission. [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] BILLING CODE 4164–01–P DEPARTMENT OF THE TREASURY 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 License. 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 Assistant Director for Compliance, 202– 622–2490. SUPPLEMENTARY INFORMATION: SUMMARY: Electronic Availability This document and additional information concerning OFAC are available on OFAC’s website: https:// ofac.treasury.gov/. 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]
BILLING CODE 4164-01-P


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