瑞士患者和公众参与学术临床研究的监管方面

Deborah Eberle, Marie Mi Bonde Hansen, Anouk Fricker, Marina Roggo
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引用次数: 0

摘要

患者和公众参与(PPI)描述了患者和公众在临床研究的不同方面的积极参与。这篇Deep Dive文章涵盖了瑞士学术临床研究中PPI的现状,给出了大学医院临床试验单位(ctu)目前提供的当地支持和倡议的例子,并解决了PPI相关立法的缺乏问题。此外,它还概述了在处理PPI期间生成的数据时要考虑的数据保护法规,并以讨论瑞士PPI相关的关键问题结束。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory aspects of patient and public involvement in academic clinical research in Switzerland
Patient and public involvement (PPI) describes the active engagement of patients and the public in different aspects of clinical research. This Deep Dive article covers the current situation of PPI in academic clinical research in Switzerland, giving examples of local support and initiatives that are currently offered by university hospital clinical trial units (CTUs) and also addressing the lack of legislation related to PPI. In addition, it provides an overview of data protection regulations to be considered when working with data generated during PPI and ends with a discussion of the key issues related to PPI in Switzerland.
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