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Product safetyFDAUnited StatesImports

International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products; Studies To Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1); Guidance for Industry; Availability

2 September 2026

In plain English

FDA announces final guidance for industry #115 (VICH GL22(R)), Revision 1, on reproduction testing to evaluate safety of veterinary drug residues in human food for veterinary drug registration.

Read the official notice
Topic
Product safety
Regulator
FDA
Published
2 September 2026
For
Imports
Where it applies
United States
Source
FDA (Food and Drug Administration)

From the notice

The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry (GFI) #115 (VICH GL22(R)) titled "Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Reproduction Testing (Revision 1)." This guidance has been developed for veterinary use by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH). The objective of this guidance is to ensure intern
The full text is at the source

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