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兽医临床试验中的知情同意获取:小型综述

Obtaining informed consent in veterinary clinical trials mini review.

作者信息

Frederick Carol E

机构信息

Cornell University Hospital for Animals, Clinical Trials, Cornell University, College of Veterinary Medicine, Ithaca, NY, United States.

出版信息

Front Vet Sci. 2024 Jun 25;11:1426014. doi: 10.3389/fvets.2024.1426014. eCollection 2024.

Abstract

In September 2023 the United States Food and Drug Administration (FDA) released draft guidance for comment about how informed client consent for companion animal clinical trials should be obtained. This guidance has the potential to substantially change how informed consent documents are written and presented to clients in the veterinary community. It provides specifics not only about how to obtain informed consent from owners but also the timeframe within which consent should be obtained, the formatting and language in the consent forms, and details on elements that are required to be in these consent forms. These changes will involve additional efforts by investigators to ensure compliance yet might lead to increased owner compliance and higher enrollment in clinical studies with subsequent benefits for all.

摘要

2023年9月,美国食品药品监督管理局(FDA)发布了征求意见稿,内容是关于如何在伴侣动物临床试验中获得客户的知情同意。该指南有可能极大地改变兽医界向客户撰写和提供知情同意文件的方式。它不仅提供了关于如何从动物主人那里获得知情同意的具体细节,还包括应在多长时间内获得同意、同意书的格式和语言,以及这些同意书中必须包含的要素细节。这些变化将要求研究人员付出更多努力以确保合规,但可能会提高动物主人的依从性,并增加临床研究的参与率,最终使各方受益。

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1
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