满足美国和欧洲供应商控制要求。

Medical device technology Pub Date : 2009-05-01
Maria Donawa
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引用次数: 0

摘要

在欧洲质量体系要求下运作的医疗器械制造商有时会惊讶地发现,他们的供应商控制程序并不完全符合美国的要求。本文讨论了美国和欧洲在控制供应商要求方面的重要差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meeting US and European supplier control requirements.

Medical device manufacturers operating under European quality system requirements are sometimes surprised to learn that their supplier control procedures do not fully meet United States (US) requirements. This article discusses important differences between US and European requirements for controlling suppliers.

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