0910-AB70 200310 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Current Good Manufacturing Practice for Medicated Feeds This proposal is in response to a citizen petition request to merge the separate requirements of the current good manufacturing practice (CGMP) regulations, 21 CFR part 225 applicable to licensed and unlicensed feed manufacturing facilities, respectively. The merger would produce a single set of updated, streamlined CGMPs that apply to all medicated feed manufacturers. This consolidation of existing CGMPs would preserve and strengthen food safety, be more appropriate given the changing structure of the medicated feed industry, and enhance uniformity and enforcement. Other Significant Previously Published in The Unified Agenda Proposed Rule Stage Undetermined Undetermined 21 CFR 225 21 USC 351 21 USC 352 21 USC 360b 21 USC 371 21 USC 374 No NPRM 06/00/2004 Undetermined Undetermined NA Not Collected George Graber 0910 Food and Drug Administration FDA 301 827-6651 ggraber@cvm.fda.gov HFV-220, Center for Veterinary Medicine, 7500 Standish Place, Rockville MD 20855