Guidance Documents will be retained in this section of the page for a period of three months. The most recently added appears first and they are in the order of the date they were issued.
Title |
Issue Date |
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Draft Guidance for Industry: The Accredited Third-Party Certification Program: Questions and Answers |
April 28, 2022 |
Guidance for Industry: Compliance with Providing an Acceptable Unique Facility Identifier for the Foreign Supplier Verification Programs for Food Importers Regulation |
April 27, 2022 |
CVM GFI #106 The Use of Published Literature in Support of New Animal Drug Approvals |
April 20, 2022 |
CVM GFI #256 - Compounding Animal Drugs from Bulk Drug Substances |
April 14, 2022 |
Use of Whole Slide Imaging in Nonclinical Toxicology Studies: Questions and Answers |
April 8, 2022 |
Guidance for Industry: Current Good Manufacturing Practice and Preventive Controls, Foreign Supplier Verification Programs, Intentional Adulteration, and Produce Safety Regulations: Enforcement Policy Regarding Certain Provisions |
March 14, 2022 |
Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart C |
March 4, 2022 |
CVM GFI #258 Use of Tracers in Animal Food, Type A Medicated Articles, and Medicated Feeds |
March 2, 2022 |
FDA's Voluntary Qualified Importer Program |
March 1, 2022 |