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解决伦理审查体系中的程序挑战:提升马来西亚临床试验审查的伦理质量。

Addressing procedural challenges of ethical review system: Towards a better ethical quality of clinical trials review in Malaysia.

机构信息

Department of Science and Technology Studies, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia.

Department of Biomedical Science, Faculty of Science, Lincoln University College, Selangor, Malaysia.

出版信息

Account Res. 2019 Jan;26(1):49-64. doi: 10.1080/08989621.2018.1556646. Epub 2018 Dec 29.

Abstract

The review of clinical trials with human participants in Malaysia is governed by a decentralized control system. The clinical trial protocols are reviewed by 13 registered research ethics committees (RECs) in Malaysia. A governmental body, the National Pharmaceutical Control Bureau, is responsible for the inspection and oversight of these registered RECs to ensure that they comply with the regulatory requirements. However, this study highlights that each REC in Malaysia has a different standard operating procedure and ethical review process. Other procedural challenges identified include inadequate membership, poor mechanism for research monitoring after ethical approval, and insufficient resources. Establishments of a national standard of REC and a central ethics committee are suggested to ensure procedural compliance in the oversight of clinical trials in Malaysia. While there is a growing concern that procedural compliance may not have a direct impact on the protection of human subjects, our key point is that an ethical review system compliant with the national standards could serve as a strong framework to support and enhance the ethical quality of decision-making and judgement. We believe that being aware of how influential procedural compliance can be would help committees improve the ethical quality of their research review.

摘要

马来西亚的人体临床试验审查由分散控制系统管理。临床试验方案由马来西亚的 13 个注册研究伦理委员会(RECs)进行审查。一个政府机构,国家药品管制局,负责检查和监督这些注册 REC,以确保它们符合监管要求。然而,这项研究强调,马来西亚的每个 REC 都有不同的标准操作程序和伦理审查过程。其他确定的程序挑战包括成员不足、伦理批准后研究监测的机制不佳以及资源不足。建议建立国家 REC 标准和中央伦理委员会,以确保在马来西亚监督临床试验时遵守程序。虽然人们越来越担心程序合规性可能不会直接影响到保护人类受试者,但我们的关键点是,符合国家标准的伦理审查系统可以作为一个强有力的框架,支持和提高决策和判断的伦理质量。我们相信,认识到程序合规性的影响力将有助于委员会提高其研究审查的伦理质量。

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