FDA Guidance Documents·· 原文未提供具体时分
Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials: Guidance for Sponsors, Clinical Investigators, and IRBs
Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials: Guidance for Sponsors, Clinical Investigators, and IRBs
AI 导读
FDA 官方历史目录记录；Final guidance；发布日期：2008-10-01。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