CFDA releases 2016 Annual Report for National Medical Device Adverse Event Monitoring

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    China Food and Drug Administration (CFDA) recently released the 2016 Annual Report for National Medical Device Adverse Event Monitoring, which includes the general situation of medical device adverse event reporting, the statistical analysis of medical device adverse events, the intensive monitoring of medical device adverse event, the quality assessment of medical device adverse event reporting, and the release of medical device vigilance newsletter in 2016. The report reflects comprehensively the performance of China’s medical device adverse event monitoring in 2016.

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