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Chinese Journal of Medical Instrumentation ; (6): 670-673, 2021.
Artículo en Chino | WPRIM | ID: wpr-922080

RESUMEN

On the basis of introducing FDA's regulatory measure and relevant requirement for life-cycle management of combination product, this paper aims to discuss corresponding countermeasure for supervision system construction in consideration of domestic drug-device combination product's current situation, in order to promote innovative development of relevant industries.


Asunto(s)
Aprobación de Recursos , Aprobación de Drogas , Estados Unidos , United States Food and Drug Administration
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