The interrelationship of sponsors, clinical investigators, and institutional review boards.

T J Kirsch
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引用次数: 2

Abstract

The responsibilities of sponsors, clinical investigators, and institutional review boards (IRBs) in the conduct of clinical research are summarized and some of the problems which each of these parties has experienced in the conduct of clinical research are described. The paper concludes with specific recommendations to secure appropriate relationships among sponsors, clinical investigators, and IRBs.

发起人、临床研究者和机构审查委员会之间的相互关系。
本文总结了临床研究的发起人、临床研究者和机构审查委员会(irb)的责任,并描述了这些各方在临床研究中所经历的一些问题。本文最后提出了具体的建议,以确保申办者、临床研究者和irb之间的适当关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
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审稿时长
6-12 weeks
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