FDA Guidance Documents·· 原文未提供具体时分
Considerations When Transferring Clinical Investigation Oversight to Another IRB: Guidance for IRBs, Clinical Investigators, and Sponsors
Considerations When Transferring Clinical Investigation Oversight to Another IRB: Guidance for IRBs, Clinical Investigators, and Sponsors
AI 导读
FDA 官方历史目录记录;Final guidance;发布日期:2014-05-23。官方主题:Good Clinical Practice (GCP)。请通过官方原文与附件查阅文件。
来源:FDA Guidance Documents · fda.gov