この記事の翻訳を準備しています。それまでの間、英語の原文を表示します。
ビジネス · 2015/4/31 分で読めます
Residual Solvents in Animal Drug Products; Questions and Answers; Guidance for Industry; Availability
ローカル自動翻訳 · 情報源の原言語
概要
The Food and Drug Administration (FDA) is announcing the availability of a guidance for industry #211 entitled "Residual Solvents in Animal Drug Products; Questions and Answers." The questions and answers 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 the Center for Veterinary Medicine's (CVM) implementation of USP Residual Solvents.
情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →