0910-AI53 202504 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. 

]]> Substantive, Nonsignificant Previously Published in The Unified Agenda Long-Term Actions No No Deregulatory 21 CFR 70 21 CFR 71 21 U.S.C. 321 21 U.S.C. 371 21 U.S.C. 379e No NPRM 09/00/2026 No No None No No No Paulette Gaynor Senior Policy Advisor 0910 Food and Drug Administration FDA 240 402-1192 301 436-2965 paulette.gaynor@fda.hhs.gov Humans Foods Program, 4300 River Road Room 2053 (HFS-255), College Park MD 20740-3835