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.
Artículo
en Chino
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Estados Unidos
/
United States Food and Drug Administration
/
Estudios de Factibilidad
/
Equipos y Suministros
/
Unión Europea
/
Legislación de Dispositivos Médicos
/
Industrias
País/Región como asunto:
America del Norte
Idioma:
Chino
Revista:
Chinese Journal of Medical Instrumentation
Año:
2022
Tipo del documento:
Artículo
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