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Negócios · 03/12/20101 min de leitura
Draft Guidance for Industry on Residual Solvents in Animal Drug Products; Questions and Answers; Availability
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Resumo
The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry 211 entitled "Residual Solvents in Animal Drug Products; Questions and Answers." The draft questions and answers (Q&A) guidance addresses the United States Pharmacopeia (USP) General Chapter Residual Solvents that applies to both human and veterinary drugs and to compendial and non- compendial drug products. This document answers questions regarding CVM's implementation of USP Residual Solvents.
Idioma original da fonte: Federal Register — Health and Human ServicesAbrir o comunicado original →