Business · 12/10/1999Updated: 10/17/2026 · 1 min read

FDA Announces Availability of VICH GL18 Draft Guidance on Residual Solvents for Veterinary Medicinal Products

Summary

The FDA is seeking public comment on a draft guidance from the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) that recommends acceptable levels of residual solvents in new animal drugs for human and animal safety.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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