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ビジネス · 2016/11/81 分で読めます

Medical Device Reporting for Manufacturers; Guidance for Industry and Food and Drug Administration Staff; Availability

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概要

The Food and Drug Administration (FDA) is announcing the availability of the guidance entitled "Medical Device Reporting for Manufacturers; Guidance for Industry and Food and Drug Administration Staff." This guidance document is intended to assist medical device manufacturers meet applicable reporting and recordkeeping requirements for certain device-related adverse events and malfunctions.

情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →

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