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 · 2009/6/241 分で読めます
The Essentials of Medical Device Regulations: A Primer for Manufacturers and Importers; Public Seminar
ローカル自動翻訳 · 情報源の原言語
概要
The Food and Drug Administration's (FDA's) Center for Devices and Radiological Health and Office of Regulatory Affairs, in cooperation with AdvaMed's Medical Technology Learning Institute, is announcing a series of three public seminars on FDA medical device regulations. These 2-day public seminars, which are designed to address the training needs of startup and small device manufacturers and their suppliers, will include both industry and FDA perspectives and a question and answer period.
情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →