CFDA releases 2015 Annual Report of National Medical Device Adverse Event Monitoring

China Food and Drug Administration (CFDA) recently released the 2015 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, and the control measures for the safety risks of medical X-ray angiography equipment, external defibrillator and low frequency electromagnetic therapy equipment. The report reflects comprehensively the performance of China’s medical device adverse event monitoring in 2015.

The report (in Chinese language) can be downloaded by following this link.