China - Regulation on Monitoring and Re-evaluation of Medical Device Adverse Event

China Food and Drug Administration have issued Regulation on Monitoring and Re-evaluation of Medical Device Adverse Event. It contains rules About the Medical Device Adverse Event Monitoring and Re-evaluation Management.

Proposed date of adoption: To be determined

Proposed date of entry into force: To be determined

Final date for comments: 60 days after circulation by the WTO Secretariat

If the Proposal/Notification/Regulation will affect your International Business please send us your representation with facts and figures before 20 February 2016, so that these can be taken up suitably.