FDA Guidance Documents·· 原文未提供具体时分
IRB Responsibilities for Reviewing the Qualifications of Investigators, Adequacy of Research Sites, and the Determination of Whether an IND/IDE is Needed: Guidance for IRBs, Clinical Investigators, and Sponsors
IRB Responsibilities for Reviewing the Qualifications of Investigators, Adequacy of Research Sites, and the Determination of Whether an IND/IDE is Needed: Guidance for IRBs, Clinical Investigators, and Sponsors
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FDA 官方历史目录记录；Final guidance；发布日期：2013-08-27。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