欧洲联盟成员国在使用转基因生物方面对医疗保健权的自主权的重要性——对欧洲联盟法院判决的分析

IF 0.2 Q4 LAW
Katja Meško Kuralt
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引用次数: 0

摘要

欧盟成员国(以下简称欧盟MS)有可能根据指令2015/412限制或禁止转基因生物的种植,但在某些条件下。欧盟MS还必须注意《欧洲联盟运作条约》或《建立欧洲共同体条约》(以下简称TFEU)的规定,这些规定与货物自由流动有关,这是欧盟运作的关键目标之一。这一贡献是基于从欧洲联盟法院(以下简称:CJEU)关于使用转基因生物(以下简称:GMO)的案例分析中获得的数据。该分析强调了环境风险评估与保健权之间的联系。本文的目的是使个人意识到他们在使用转基因生物方面的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Importance of Autonomy of European Union Member States with regard to the Use of Genetically Modified Organisms on the Right to Healthcare – An Analysis of Judgements of the Court of Justice of the European Union
The European Union Member States (hereinafter: EU MS) have the possibility of restricting or banning the cultivation of GMOs under the Directive 2015/412 but under certain conditions. EU MS must also pay attention to the provisions of the Treaty on the Functioning of the Euro-pean Union or Treaty Establishing the European Community (hereinafter: TFEU), the provi-sions relating to the free movement of goods, which is one of the key objectives of the func-tioning of the European Union. This contribution is based on the data obtained from an analy-sis of Court of Justice of the European Union (hereinafter: CJEU) cases concerning the use of genetically modified organisms (hereinafter: GMO(s)). The analysis highlights the link between environmental risk assessment and the right to healthcare. The purpose of this paper is to make the individual aware of the possibilities they have regarding the use of GMOs.
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Lexonomica
Lexonomica LAW-
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