Business · 03/12/2010Updated: 10/17/2026 · 1 min read
FDA Releases Draft Guidance on Residual Solvents in Animal Drug Products
Summary
The Food and Drug Administration (FDA) has made available a draft guidance document (FDA Draft Guidance No. 211) addressing residual solvents in animal drug products, including questions and answers regarding the implementation of USP General Chapter Residual Solvents for both human and veterinary drugs.
Original source language: Federal Register — Health and Human ServicesOpen original release →