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The Force of Law: Genetic Data Protection in Central and Eastern Europe

机译:法律力量:中欧和东欧的遗传数据保护

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During the past decade the collection and processing of human biological samples and that of related data gained an increasingly important role in both medical research and the forensic field. Th e European Union legislator tried to keep up with this phenomenon, and attempted to reconcile freedom of research in the classical biobank context and the principle of availability in the criminal context with European Union-wide data protection safeguards. In the lack of a sufficiently homogeneous legal framework European jurisdictions greatly differ in regulating the protection of genetic data. Two main country groups can be identified: Member States can be grouped along the question whether they have or do not have specific biobank laws. In countries that do have such laws, comparison is easier, and they are following international standards. Whenever such specific laws are lacking, not only the identification of the respective legal rules, but also their comparison is difficult, since the interpretation of these vague and more general laws is left to the stakeholders, law enforcement agencies, and finally to the judiciary. Since in this latter group of countries however relevant judicial cases are very rare, the interpretation of the codes and other comprehensive laws happens on an ad hoc basis, and remains invisible. Th e differing legal and ethical issues concerning patients’ data in the classical context, and suspects’, convicts’, victims’ and other persons’ data protection in a forensic context will be addressed in light of the 2003 International Declaration on Human Genetic Data. Actual examples from Central European jurisdictions will highlight the related theoretical and practical problems both in terms of bioethical research and forensic sciences on the one hand and data protection and privacy on the other.
机译:在过去的十年中,人类生物样本以及相关数据的收集和处理在医学研究和法医领域都发挥着越来越重要的作用。欧盟立法者试图跟上这一现象,并试图在传统生物库的背景下将研究自由与在刑事背景下的可得性原则与欧盟范围内的数据保护措施相协调。在缺乏足够统一的法律框架的情况下,欧洲管辖区在规范遗传数据保护方面存在很大差异。可以确定两个主要的国家组:可以根据问题将成员国分组,看看它们是否有专门的生物库法律。在拥有此类法律的国家/地区,比较起来比较容易,并且遵循国际标准。每当缺少这些具体法律时,不仅要确定各自的法律规则,而且要进行比较也很困难,因为对这些含糊不清和更笼统的法律的解释留给了利益相关者,执法机构,最后是司法部门。由于在这后一组国家中,相关的司法案件非常少见,因此对守则和其他全面法律的解释是临时性的,并且仍然是看不见的。在经典情况下,有关患者数据的法律和道德问题各不相同,在法医情况下,嫌疑人,定罪者,受害者和其他人的数据保护将根据2003年《国际人类基因数据宣言》解决。来自中欧司法管辖区的实际案例一方面将突出相关的理论和实践问题,一方面是在生物伦理学研究和法医学方面,另一方面是在数据保护和隐私方面。

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