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 · 2016/11/21 分で読めます
Animal Drug User Fees and Fee Waivers and Reductions; Draft Revised 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 or Agency) is announcing the availability of a draft revised guidance for industry (GFI) #170 entitled "Animal Drug User Fees and Fee Waivers and Reductions." This draft revised guidance document describes the types of fees the Food and Drug Administration (FDA or the Agency) is authorized to collect under the Animal Drug User Fee Act of 2003 (ADUFA), as amended, and how to request waivers and reductions from these fees.
情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →