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HHS/FDA

RIN: 0910-AB70

Publication ID: Fall 2003

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

Timetable: Action Date FR Cite NPRM  06/00/2004

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 Email: ggraber@cvm.fda.gov