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HHS/FDA RIN: 0910-AB70 Publication ID: Spring 2002 
Title: Current Good Manufacturing Practice for Medicated Feeds 
Abstract: 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. 
Agency: Department of Health and Human Services(HHS)  Priority: Other Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: Undetermined  Unfunded Mandates: Undetermined 
CFR Citation: 21 CFR 225   
Legal Authority: 21 USC 351    21 USC 352    21 USC 360b    21 USC 371    21 USC 374   
Legal Deadline:  None
Action Date FR Cite
NPRM  01/00/2003    
Regulatory Flexibility Analysis Required: Undetermined  Government Levels Affected: Undetermined 
Federalism: Undetermined 
Included in the Regulatory Plan: No 
Agency Contact:
George Graber
Director, Division of Animal Feeds
Department of Health and Human Services
Food and Drug Administration
HFV-220, Center for Veterinary Medicine, 7500 Standish Place,
Rockville, MD 20855
Phone:301 827-6651

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