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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 |
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Timetable:
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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 |