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  1. Guidance & Regulations

Policies & Procedures Manual

These pages provide sections of the CVM Program Policy and Procedures and the Office of New Animal Product Evaluation and Office of Generic Animal Drugs Reviewer’s Chapter.  The Manual provides a quick reference to the rules, regulations, and instructions pertinent to all program areas of CVM's responsibilities, including the review of new animal drug applications, and post-market surveillance and compliance activities. All of the linked sections are available in pdf format only.

CVM FUNCTIONAL STATEMENTS

1500 - OCCUPATIONAL SAFETY AND HEALTH

2000 - POLICY FORMATION

2100 - ADMINISTRATION

2200 - GENERAL REGULATORY

PPM NUMBERTITLEDATE
1240.2202Voluntary Compliance08/11/1992

2300 - COMMUNICATION

2500 - FREEDOM OF INFORMATION

2600 - SPECIAL INTERESTS

3100 - NADA

3300 - FOOD ADDITIVE PETITION

3400 - ANIMAL FEEDS

3500 - SURVEILLANCE

3600 - COMPLIANCE

3700 - RESEARCH

4000 - LABELING

PPM NUMBERTITLEDATE
1240.4010Antibacterials Labeled for Secondary Infections09/10/1997
1240.4020Uniformity in Labeling (retired on 2/18/2026)09/10/1997
1240.4021General Policies for Animal Drug Label Review (retired on 2/18/2026)09/10/1997
1240.4023Notifying Sponsors When Approved Supplemental Labeling Changes in an Upstream Drug Application ((A)NADA) Approved for Use in or on Animal Feed will Require Revisions to Approved Downstream Labeling Components04/01/2024
1240.4025Therapeutic Use Directions for Medicated Feed and Drinking Water (retired on 2/18/2026)09/10/1997
1240.4030Established Names (retired on 01/20/2026)09/10/1997
1240.4040Clinical Investigator Sanctions and the Videotex Method Of Obtaining Information on Ineligible Investigators09/10/1997

4100 - DRUGS

4200 - AQUACULTURE

 



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