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Research on the Necessity and Feasibility of Current Medical Device Supervision Legislation / 中国医疗器械杂志
Chinese Journal of Medical Instrumentation ; (6): 433-437, 2022.
Article in Chinese | WPRIM | ID: wpr-939762
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: United States / United States Food and Drug Administration / Feasibility Studies / Equipment and Supplies / European Union / Medical Device Legislation / Industry Country/Region as subject: North America Language: Chinese Journal: Chinese Journal of Medical Instrumentation Year: 2022 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: United States / United States Food and Drug Administration / Feasibility Studies / Equipment and Supplies / European Union / Medical Device Legislation / Industry Country/Region as subject: North America Language: Chinese Journal: Chinese Journal of Medical Instrumentation Year: 2022 Type: Article