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Access to Routinely Collected Clinical Data for Research: A Process Implemented at an Academic Medical Center

机译:获得常规收集的研究临床数据:在学术医疗中心实施的过程

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摘要

Electronic health records are valuable for clinical and translational research. Institutions must protect patient privacy and comply with applicable regulations while allowing appropriate access to clinical data for research. The processes that investigators must follow to access clinical data can be substantially different at different institutions. In this paper, we describe the process developed at our institution that has been active for 5 years and was used to satisfy over 200 requests for access to identified clinical data, usually within 1 day for internal requests and 3 days for visiting researchers.
机译:电子健康记录对临床和翻译研究有价值。 机构必须保护患者隐私,并遵守适用的法规,同时允许适当访问研究的临床数据。 调查人员必须遵循的过程在进入临床数据中可能在不同的机构中具有基本不同。 在本文中,我们描述了在我们的机构开发的过程,该过程已经活跃了5年,用于满足200多个可获得鉴定的临床资料的请求,通常在1天内的内部请求和访问研究人员进行3天。

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