21 CFR Part 500 - GENERAL
- SUBPART A — [Reserved]
- SUBPART B — Specific Administrative Rulings and Decisions (§§ 500.23 - 500.50)
- SUBPART C — Animal Drug Labeling Requirements (§§ 500.51 - 500.55)
- SUBPART D — Requirements for Specific Animal Drugs (§§ 500.65 - 500.65)
- SUBPART E — Regulation of Carcinogenic Compounds Used in Food-Producing Animals (§§ 500.80 - 500.92)
- SUBPART F — Methods for Detection of Residues of Carcinogenic Compounds Used in Food-Producing Animals (§§ 500.1410 - 500.1410)
Title 21 published on 2012-04-01
The following are only the Rules published in the Federal Register after the published date of Title 21.
For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.
Title 21 published on 2012-04-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 500 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2012-29322 RIN 0910-AG17 Docket No. FDA-2012-N-1067 DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Proposed rule. Submit either electronic or written comments by March 5, 2013. See section VI of this document for the proposed effective date of a final rule based on this proposed rule. 21 CFR Parts 500, 520, 522, 524, 529, 556, and 558 The Food and Drug Administration (FDA) is proposing to revise the animal drug regulations regarding tolerances for residues of approved and conditionally approved new animal drugs in food by standardizing, simplifying, and clarifying the determination standards and codification style. In addition, we are 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.
GPO FDSys XML | Text type regulations.gov FR Doc. 2012-20609 RIN Docket No. FDA-2010-N-0612 DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Final rule. This rule is effective September 21, 2012. 21 CFR Part 500 The Food and Drug Administration (FDA) is amending its regulations regarding compounds of carcinogenic concern used in food-producing animals. Specifically, the Agency is clarifying the definition of “S o ” and revising the definition of “S m ” so that it conforms to the clarified definition of S o . Other clarifying and conforming changes are also being made.