FDA Guidance Documents·· 原文未提供具体时分
Questions and Answers on Informed Consent Elements, 21 CFR § 50.25(c): Guidance for Sponsors, Investigators, and Institutional Review Boards
Questions and Answers on Informed Consent Elements, 21 CFR § 50.25(c): Guidance for Sponsors, Investigators, and Institutional Review Boards
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FDA 官方历史目录记录；Final guidance；发布日期：2012-02-01。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