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首页|期刊导航|中华医学杂志(英文版)|Acceptance of overseas clinical trial data of medical devices for pre-market registration:general principles and considerations of the National Medical Products Administration

Acceptance of overseas clinical trial data of medical devices for pre-market registration:general principles and considerations of the National Medical Products Administration

Shan Ju Ying-Hui Liu Yi-Dan Zhang Chuan-Song Wu Li Xiao Lei Sun

中华医学杂志(英文版)2021,Vol.134Issue(18):2163-2165,3.
中华医学杂志(英文版)2021,Vol.134Issue(18):2163-2165,3.DOI:10.1097/CM9.0000000000001595

Acceptance of overseas clinical trial data of medical devices for pre-market registration:general principles and considerations of the National Medical Products Administration

Acceptance of overseas clinical trial data of medical devices for pre-market registration:general principles and considerations of the National Medical Products Administration

Shan Ju 1Ying-Hui Liu 2Yi-Dan Zhang 1Chuan-Song Wu 2Li Xiao 2Lei Sun2

作者信息

  • 1. Department of Clinical and Biostatistics Ⅰ,Center for Medical Device Evaluation National Medical Products Administrition,Beijing 100081,China
  • 2. Center for Medical Device Evaluation National Medical Products Administrition,Beijing 100081,China
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摘要

引用本文复制引用

Shan Ju,Ying-Hui Liu,Yi-Dan Zhang,Chuan-Song Wu,Li Xiao,Lei Sun..Acceptance of overseas clinical trial data of medical devices for pre-market registration:general principles and considerations of the National Medical Products Administration[J].中华医学杂志(英文版),2021,134(18):2163-2165,3.

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