Passive medical devices
2021-03-25
National Medical Products Administration on the release of medical device registrants to carry out adverse event monitoring
- Categories:Industry dynamic
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- Time of issue:2021-03-15
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(Summary description)In order to implement the requirements of Administrative Measures for Monitoring and Reevaluation of Adversant Medical Device Events (Order No. 1 of the State Administration for Market Regulation, the National Health Commission, PRC), the registrant and record holder of medical device (hereinafter referred to as the registrant) shall be guided and standardized.
National Medical Products Administration on the release of medical device registrants to carry out adverse event monitoring
(Summary description)In order to implement the requirements of Administrative Measures for Monitoring and Reevaluation of Adversant Medical Device Events (Order No. 1 of the State Administration for Market Regulation, the National Health Commission, PRC), the registrant and record holder of medical device (hereinafter referred to as the registrant) shall be guided and standardized.
- Categories:Industry dynamic
- Author:
- Origin:
- Time of issue:2021-03-15
- Views:0
Information
In order to implement the requirements of Administrative Measures for Monitoring and Reevaluation of Adversant Medical Device Events (Order No. 1 of the State Administration for Market Regulation, the National Health Commission, PRC), the registrant and record holder of medical device (hereinafter referred to as the registrant) shall be guided and standardized.
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