克服障碍,从临床试验中获得更好的证据

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Lindsay Kehoe, Trevan Locke, Mark McClellan, Martin Landray, Adrian Hernandez, Sally Okun
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引用次数: 0

摘要

通过提高研究的可及性和试验参与的便利性,可以改善从具有代表性的人群中产生临床证据的工作。为了提高研究的可及性和参与度,需要建立现代化的试验基础设施,将研究扩展到更多的常规实践中。本评论强调了目前存在的障碍、取得进展的领域以及为改进证据生成系统而继续向现代试验基础设施转型所需的行动。本评论的重点是美国医疗产品(如药物、器械、生物制剂)的开发和基础设施问题,旨在使其具有更广泛的跨国适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overcoming the barriers to better evidence generation from clinical trials
Clinical evidence generation from and for representative populations can be improved through increased research access and ease of trial participation. To improve access and participation, a modern trial infrastructure is needed that broadens research into more routine practice. This commentary highlights current barriers, areas of advancement, and actions needed to enable continued transformation toward a modern trial infrastructure for an improved evidence generation system. The focus of this commentary is on the development of medical products (e.g., drugs, devices, biologics) and infrastructure issues within the United States, with the aim to have broader, multi-national applicability.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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