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비즈니스 · 2010. 12. 3.1 분 읽기
Draft Guidance for Industry on Residual Solvents in Animal Drug Products; Questions and Answers; Availability
로컬 자동 번역 · 원본 출처 언어
요약
The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry 211 entitled "Residual Solvents in Animal Drug Products; Questions and Answers."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.
원본 출처 언어: Federal Register — Health and Human Services원문 발표 열기 →