自中国食品药品监督管理总局出台医疗器械审批程序以来

Tobias Lueddemann, Diqing Chang, S. Şahin, T. Lueth
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引用次数: 3

摘要

近十年来,中国医疗器械市场持续增长,对国外医疗器械制造商的吸引力越来越大。然而,由于快速变化的监管环境和缺乏可用的英文信息和文件,作为外国制造商在中国营销产品具有挑战性。本文介绍了中国食品药品监督管理局(CFDA)的最新情况,并在对CFDA中文原始文件进行研究的基础上,介绍了当前的CFDA审批流程和所需文件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medical device approval process in China since the introduction of the China Food and Drug Administration
China's medical device market is continuously growing since the last decade and increasingly attractive for foreign medical device manufacturers. However, marketing products in China as a foreign manufacturer is challenging due to the rapidly changing regulatory environment and lack of available information and documents published in English. This work addresses the recent introduction of the China Food and Drug Administration (CFDA) and presents the current CFDA approval processes and required documentation based on research of the original documents of the CFDA in Chinese language.
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