← Back to FR Documents
Final Rule

Advisory Committee; Science Advisory Board to the National Center for Toxicological Research; Termination; Removal From List of Standing Committees

Final rule.

📖 Research Context From Federal Register API

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.

Key Dates
Citation: 89 FR 46802
This rule is effective May 30, 2024.
Public Participation
Topics:
Administrative practice and procedure Advisory committees Color additives Drugs Radiation protection

In Plain English

What is this Federal Register notice?

This is a final rule published in the Federal Register by Health and Human Services Department, Food and Drug Administration. Final rules have completed the public comment process and establish legally binding requirements.

Is this rule final?

Yes. This rule has been finalized. It has completed the notice-and-comment process required under the Administrative Procedure Act.

Who does this apply to?

Final rule.

When does it take effect?

This document has been effective since May 30, 2024.

Document Details

Document Number2024-11811
FR Citation89 FR 46802
TypeFinal Rule
PublishedMay 30, 2024
Effective DateMay 30, 2024
RIN-
Docket IDDocket No. FDA-2024-N-2357
Pages46802–46802 (1 pages)
Text FetchedYes

Agencies & CFR References

CFR References:

Linked CFR Parts

PartNameAgency
21 CFR 14 Public Hearing Before a Public Advisory ... -

Paired Documents

TypeProposedFinalMethodConf
No paired documents

External Links

⏳ Requirements Extraction Pending

This document's regulatory requirements haven't been extracted yet. Extraction happens automatically during background processing (typically within a few hours of document ingestion).

Federal Register documents are immutable—once extracted, requirements are stored permanently and never need re-processing.

Full Document Text (650 words · ~4 min read)

Text Preserved
<RULE> DEPARTMENT OF HEALTH AND HUMAN SERVICES <SUBAGY>Food and Drug Administration</SUBAGY> <CFR>21 CFR Part 14</CFR> <DEPDOC>[Docket No. FDA-2024-N-2357]</DEPDOC> <SUBJECT>Advisory Committee; Science Advisory Board to the National Center for Toxicological Research; Termination; Removal From List of Standing Committees</SUBJECT> <HD SOURCE="HED">AGENCY:</HD> Food and Drug Administration, HHS. <HD SOURCE="HED">ACTION:</HD> Final rule. <SUM> <HD SOURCE="HED">SUMMARY:</HD> 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. </SUM> <EFFDATE> <HD SOURCE="HED">DATES:</HD> This rule is effective May 30, 2024. </EFFDATE> <FURINF> <HD SOURCE="HED">FOR FURTHER INFORMATION CONTACT:</HD> 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, <E T="03">Ashley.Groves@fda.hhs.gov.</E> </FURINF> <SUPLINF> <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD> 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. <LSTSUB> <HD SOURCE="HED">List of Subjects in 21 CFR Part 14</HD> Administrative practice and procedure, Advisory committee, Color additives, Drugs, Radiation protection. </LSTSUB> 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: <HD SOURCE="HED">PART 14—PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE</HD> <REGTEXT TITLE="21" PART="14"> 1. The authority citation for part 14 continues to read as follows: <HD SOURCE="HED">Authority: </HD> 5 U.S.C. 1001 <E T="03">et seq.;</E> 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. </REGTEXT> <REGTEXT TITLE="21" PART="14"> <SECTION> <SECTNO>§ 14.100</SECTNO> <SUBJECT>[Amended]</SUBJECT> </SECTION> </REGTEXT> <REGTEXT TITLE="21" PART="14"> 2. Amend § 14.100 by removing paragraph (e). </REGTEXT> <SIG> <DATED>Dated: May 23, 2024.</DATED> <NAME>Lauren K. Roth,</NAME> Associate Commissioner for Policy. </SIG> </SUPLINF> <FRDOC>[FR Doc. 2024-11811 Filed 5-29-24; 8:45 am]</FRDOC> </RULE>
This text is preserved for citation and comparison. View the official version for the authoritative text.