Seminar on China's New Regulations of Medical Device

2014-08-30 | Beijing

To prepare for this seminar, EUCCC, jointly with Amcham, as well as China Association for Medical Device Industry (CAMDI), had meetings with members and consolidated comments / suggestions, and submitted to CFDA, requesting for clarification/advice from CFDA during the seminar.

Mr. Zhang introduced overall revisions of medical device regulations from Legal perspective. SUN briefed about ideas for post-market surveillance supervision, manufacturing, distributing. DENG presented mainly for medical device registration regulations’ revision.