机构审查委员会的见解:提交给机构审查委员会的提示。

IF 2.1 Q1 Nursing
Allison M Wiedeman, Benjamin Rocky Byington, Saima Deen, Hadley Sauers-Ford
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引用次数: 0

摘要

机构审查委员会(IRB)是儿科研究过程中必不可少的合作者。为了产生有意义的结果,研究必须在科学上和伦理上合理,IRB的责任是审查和批准人类受试者的研究,同时保护受试者的权利,将研究风险降到最低,并使收益最大化。了解研究批准程序对任何希望进行人类受试者研究的临床研究者都很重要。虽然IRB的要求可以,而且经常会因地点而异,但是有一些重要的总体要求适用于所有的机构。我们的目标是通过三个部分提供关于如何通过IRB流程导航研究的一般实用指导:在开始研究文件之前要考虑什么,在起草文件时要考虑什么,以及提交后会发生什么。我们希望这些有用的提示能够有效地对拟议的研究和成功的科学进行IRB审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Institutional Review Board Insights: Tips for Submission to the Institutional Review Board.

The institutional review board (IRB) is an essential collaborator in the pediatric research process. Research must be scientifically and ethically sound to produce meaningful results, and it is the IRB's responsibility to review and approve human subjects' research while protecting the subjects' rights, minimizing research risks, and maximizing the benefits. Understanding the research approval process is important for any clinician investigator hoping to conduct human subjects' research. Although IRB requirements can, and often do, vary by site, there are important overarching requirements that apply to all institutions. We aim to provide general, practical guidance on how to navigate a study through the IRB process in 3 sections: what to consider before starting your study documents, what to consider while drafting documents, and what happens after you submit. Our hope is that these helpful hints lead to efficient IRB review of proposed research and successful science.

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来源期刊
Hospital pediatrics
Hospital pediatrics Nursing-Pediatrics
CiteScore
3.70
自引率
0.00%
发文量
204
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