Yue Wei
Shanghai Municipal Food and Drug Administration.
Zhongguo Yi Liao Qi Xie Za Zhi. 2009 Jan;33(1):51-8.
The paper compares the medical device registration system between China and FDA in U.S.A., with the main focus on the problems of design default of supervision and management in Chinese system. It analyzes the primary elements of substantial equivalence approval in medical device registration, and points out the design defaults of our medical device registration system and the basic points which need to be handled.
本文比较了中国与美国食品药品监督管理局(FDA)的医疗器械注册制度,主要关注中国制度中监管设计的缺陷问题。分析了医疗器械注册中实质等同性审批的主要因素,指出了我国医疗器械注册制度的设计缺陷以及需要处理的要点。