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HHS/FDA | RIN: 0910-AG17 | Publication ID: Fall 2015 |
Title: New Animal Drugs: Updating Tolerances for Residues in New Animal Drugs in Food | |
Abstract: FDA is proposing to revise the animal drug regulations regarding tolerances for residues of approved and conditionally approved applications for conditional approval of new animal drugs in food by standardizing, simplifying, and clarifying the determination standards and codification style. In addition, the Agency is proposing to add definitions for key terms. The purpose of the revision is to enhance understanding of tolerance determination and improve the readability of the regulations. | |
Agency: Department of Health and Human Services(HHS) | Priority: Routine and Frequent |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Proposed Rule Stage |
Major: No | Unfunded Mandates: No |
CFR Citation: 21 CFR 556 | |
Legal Authority: 21 U.S.C. 342 21 U.S.C. 360b 21 U.S.C. 371 |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: No | Government Levels Affected: None |
Small Entities Affected: No | Federalism: No |
Included in the Regulatory Plan: No | |
RIN Data Printed in the FR: No | |
Agency Contact: Dong Yan Biologist Department of Health and Human Services Food and Drug Administration Center for Veterinary Medicine, MPN-2, HFV-151, 7500 Standish Place, Rockville, MD 20855 Phone:240 402-0825 Email: dong.yan@fda.hhs.gov |