Analysis on Re-classifcation Management Procedure of Medical Devices in the United States / 中国医疗器械杂志
Chinese Journal of Medical Instrumentation
; (6): 118-121, 2019.
Article
em Zh
| WPRIM
| ID: wpr-772549
Biblioteca responsável:
WPRO
ABSTRACT
A detailed analysis on re-classification procedure of medical devices from Food and Drug Administration.The experience on classification procedures,the work-flow of risk reanalysis and regulatory categories reassessment of listed products,as well as launching a comprehensive evaluation and downgrading of listed high-risk products were explored in recent years.Based on the analysis on classification procedures and supervision of medical device products in the USA,and combined with the current situation of classification of medical devices in China,some suggestions were put forward on the current classification mode of medical devices so as to improve the quality and efficiency of classified management of medical devices in China.
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Texto completo:
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Índice:
WPRIM
Assunto principal:
Estados Unidos
/
United States Food and Drug Administration
/
China
/
Equipamentos e Provisões
/
Segurança de Equipamentos
País/Região como assunto:
America do norte
/
Asia
Idioma:
Zh
Revista:
Chinese Journal of Medical Instrumentation
Ano de publicação:
2019
Tipo de documento:
Article