0910-AI53 202304 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Amendment of Procedural Requirements for Color Additive Petitions

The Food and Drug Administration (FDA) is proposing to amend procedural requirements for color additive petitions (CAPs). This action, if finalized, would modernize the procedural requirements related to the data requirements, submission procedures, review process, and regulatory timeframes for CAPs. 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.

]]> Substantive, Nonsignificant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 70 21 CFR 71 21 U.S.C. 321 21 U.S.C. 371 21 U.S.C. 379e No NPRM 04/00/2024 No No None No No No Annette McCarthy Lead Biologist, NEPA Specialist 0910 Food and Drug Administration FDA 240 402-1057 annette.mccarthy@fda.hhs.gov Human Foods Program, 5001 Campus Drive, College Park MD 20740