FDA Guidance Documents·· 原文未提供具体时分
Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers: Guidance for Institutional Review Boards, Investigators, and Sponsors
Use of Electronic Informed Consent in Clinical Investigations – Questions and Answers: Guidance for Institutional Review Boards, Investigators, and Sponsors
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FDA 官方历史目录记录；Final guidance；发布日期：2016-12-15。官方主题：Administrative / Procedural。请通过官方原文与附件查阅文件。
来源：FDA Guidance Documents · fda.gov