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EU : Commission plans to 'move from directives to regulations'for medtech sector

机译:欧盟:委员会计划为医疗技术行业“从指令过渡到法规”

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The European Commission has revealed that it intends to propose "two regulations" to improve the current oversight of the EU medtech sector."We are going to move from directives to regulations," Jacqueline Minor, the director of consumer policy at the commission's DG Sanco said during the UK Parliament's Science and Technology Committee (STC) hearing on 13 June.Moving from directives to regulations would mean that no national legislation would be required to translate the rules into the legal systems of the [EU] member states, "which will eliminate to some degree differences of interpretation or of application", Ms Minor said. The commission intends to table its proposal for a new EU regulatory framework in late September
机译:欧盟委员会透露,它打算提出“两项法规”,以改善目前对欧盟医疗技术领域的监督。“我们将从指令转向法规,”欧盟委员会DG Sanco消费者政策主管Jacqueline Minor在6月13日英国议会科学与技术委员会(STC)的听证会上说。从指令移至法规将意味着不需要任何国家立法就可以将规则转化为[EU]成员国的法律体系,“消除某种程度上解释或应用上的差异”,米诺女士说。该委员会计划在9月下旬提交其有关新欧盟监管框架的提案

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