FDA Guidance Documents·· 原文未提供具体时分
In Vitro Diagnostic (IVD) Device Studies - Frequently Asked Questions: Guidance for Industry and FDA Staff
In Vitro Diagnostic (IVD) Device Studies - Frequently Asked Questions: Guidance for Industry and FDA Staff
AI 导读
FDA 官方历史目录记录；Final guidance；发布日期：2010-06-25。官方主题：Premarket, Good Clinical Practice (GCP), Laboratory Tests, IVDs (In Vitro Diagnostic Devices)。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov