通用数据保护条例对临床研究和知情同意的影响综述

Giannuzzi, Annalisa Landi, F. Bartoloni, A. Ceci
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引用次数: 3

摘要

为了协调整个欧洲的个人数据保护法律,新的《欧洲通用数据保护条例(GDPR)条例》(EU)2016/679废除了数据保护指令95/46/EC。GDPR将允许对相当多的欧盟公民进行数据保护。通过这种方式,《条例》也将影响临床调查,特别是提供同意的信息过程。本文阐述了《通用数据保护条例》产生的主要变化,并就如何处理知情同意书和同意文件提供了实际信息。提供了关于儿科研究和二次使用的特别聚光灯。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review on Impact of General Data Protection Regulation on ClinicalStudies and Informed Consent
To harmonise personal data protection laws throughout the Europe, the Data Protection Directive 95/46/EC has been repealed by the new European General Data Protection Regulation (GDPR) Reg. (EU) 2016/679. GDPR will allow the data protection of the considerable number of citizens of the European Union. In this way, the Regulation will effect also on clinical investigations, and specifically, on the information process to provide consent. This paper goes to elucidating the main changes derived by the GDPR and to giving practical information on how to deal with informed consent and assent documents in concurrence with the regulation. Special spotlights on paediatric research and secondary use have been provided.
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