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HHS/FDA | RIN: 0910-AI55 | Publication ID: Spring 2023 |
Title: Amendment of Procedural Requirements for Food Additive Petitions | |
Abstract:
The Food and Drug Administration (FDA) is proposing to amend sections of our food additive and food additive petition (FAPs) regulations to modernize the procedural requirements related to the data requirements, submission procedures, review process, and regulatory timeframes for FAPs. FDA is proposing to revise the regulations to provide additional transparency, streamline current procedures, ease regulatory burden, and modernize the regulations. The proposed rule, if finalized, would improve regulatory efficiencies by implementing petition data requirements that are specific to the requested action. |
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Agency: Department of Health and Human Services(HHS) | Priority: Substantive, Nonsignificant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Proposed Rule Stage |
Major: No | Unfunded Mandates: No |
CFR Citation: 21 CFR 170 21 CFR 171 | |
Legal Authority: 21 U.S.C. 321 21 U.S.C. 348 21 U.S.C. 371 |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: No | Government Levels Affected: None |
Small Entities Affected: No | Federalism: No |
Included in the Regulatory Plan: No | |
RIN Data Printed in the FR: No | |
Agency Contact: Annette McCarthy Consumer Safety Officer Department of Health and Human Services Food and Drug Administration 5001 Campus Drive, College Park, MD 20740 Phone:240 402-1057 Email: annette.mccarthy@fda.hhs.gov |