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在ClinicalTrials.gov上发布的知情同意表格中的关键信息部分的描述

Luke Gelinas1,2, Walker Morrell2, Tony Tse3

  • 1Advarra Inc., Columbia, MD, USA.

Journal of clinical and translational science
|September 25, 2023
PubMed
概括

新的美国联邦规则要求在人类研究的知情同意表格 (ICF) 中有一个关键信息 (KI) 部分. 这项研究分析了联邦资助的试验中的KI部分,发现它们通常与指南保持一致,但可以通过更清晰的写作来改进.

关键词:
经过知情同意的同意.一个共同的规则.伦理学 伦理 伦理学关键信息 关键信息规则 条例 条例 规章 规章 规章

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