FDA Guidance Documents·· 原文未提供具体时分
Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects: Guidance for Industry
Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects: Guidance for Industry
AI 导读
FDA 官方历史目录记录；Final guidance；发布日期：2009-10-23。官方主题：Administrative / Procedural, 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