我们能对死者的数据做些什么?规范性建议书

IF 0.2 Q4 LAW European Review of Private Law Pub Date : 2021-10-01 DOI:10.54648/erpl2021041
Í. de Miguel Beriain, A. Duardo-Sánchez, José Antonio Castillo Parrilla
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引用次数: 0

摘要

死者的健康和基因数据是生物医学研究领域的一项特别重要的资产。然而,在实践中,使用它们是复杂的,因为规范其使用的法律框架尚未完全制定。《通用数据保护条例》(GDPR)不适用于此类数据,成员国也未能就替代条例达成一致。最近,为了应对这一问题,提出了规范性模型。其中最著名的是死后医疗数据捐赠(PMDD)。该提案支持为研究目的选择捐赠健康数据的系统。在这篇文章中,我们认为PMDD不是解决当前问题的有用模型,因为它没有考虑到其中一些数据(基因数据)可能是死者在世亲属的个人数据。此外,我们发现支持选择加入模型的理由不如那些保证替代系统的理由令人信服。事实上,我们提出了一个规范性框架,该框架基于非个人数据的选择退出制度,并结合GDPR对亲属个人数据的应用。
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What Can We Do with the Data of Deceased People? A Normative Proposal
The health and genetic data of deceased people are a particularly important asset in the field of biomedical research. However, in practice, using them is complicated, as the legal framework that should regulate their use has not been fully developed yet. The General Data Protection Regulation (GDPR) is not applicable to such data and the Member States have not been able to agree on an alternative regulation. Recently, normative models have been proposed in an attempt to face this issue. The most wellknown of these is posthumous medical data donation (PMDD). This proposal supports an opt-in donation system of health data for research purposes. In this article, we argue that PMDD is not a useful model for addressing the issue at hand, as it does not consider that some of these data (the genetic data) may be the personal data of the living relatives of the deceased. Furthermore, we find the reasons supporting an opt-in model less convincing than those that vouch for alternative systems. Indeed, we propose a normative framework that is based on the opt-out system for non-personal data combined with the application of the GDPR to the relatives’ personal data.
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来源期刊
CiteScore
0.40
自引率
33.30%
发文量
25
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