FDA Guidance Documents·· 原文未提供具体时分
Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff
Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff
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FDA 官方历史目录记录；Final guidance；发布日期：2014-02-13。官方主题：Adverse Event Reporting System (FAERS), Adverse Event Reporting。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov