在临床研究中使用电子病历系统的全国调查

Elke Hiendlmeyer
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引用次数: 0

摘要

每天,越来越多的健康数据以电子方式被捕获和记录,而不是像以前那样成堆地打印出来。在不久的将来,我们有望实现从纸质记录到电子记录的全面过渡。然而,这种数字化的进步远远超出了获取患者记录的最初步骤。健康数据是临床试验的基本组成部分。因此,如何选择和收集数据的做法与临床试验的监管要求以及如何从操作角度运行这些试验密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A national survey on the use of EHR systems in clinical research
Every day, more and more health data are captured and documented electronically instead of in stacks of printouts, as it often once was. The near future promises a full transition from paper to electronic records. This digital progress is felt far beyond the initial steps of capturing patient records, however. Health data are a fundamental building block of clinical trials. So the practices of how data are selected and collected are closely linked to the regulatory requirements of clinical trials and how these trials will be run from an operational standpoint.
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