对我国当前医疗器械监管立法的必要性和可行性研究

      Research on the Necessity and Feasibility of Current Medical Device Supervision Legislation

      • 摘要: 从加强依法行政,保护公众健康,健全医药法律体系和促进医疗器械行业发展等角度对我国当前医疗器械监管立法的必要性进行了研究,分析和总结美国、欧盟和日本等国家和地区医疗器械监管领域的立法经验和立法形式,认为从立法的政治保障、现实基础、探索和国际经验等方面来看,我国当前开展对医疗器械监管立法的条件已经比较成熟,并且为我国《医疗器械管理法》的出台提出了立法原则和立法形式等方面的政策建议。

         

        Abstract: This paper studies the necessity of the current legislation on the supervision of medical devices in China from the perspectives of strengthening administration according to law, protecting public health, perfecting the legal system of medicine and promoting the development of the medical device industry. This study analyzes and summarizes the legislative experiences and forms in the field of medical device regulation in the United States, the European Union, Japan and other countries and regions, at present, the conditions of carrying out the legislation of medical device supervision in China are quite mature, and some policy suggestions are put forward for the enactment of the law of medical device management in China.

         

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