A summary on main EU-China cooperation activities in medical device sector from industry perspective was submitted to CFDA

2016-04-20 | Beijing

Upon the request from CFDA, a summary about EU-China cooperation from medical device regulatory perspective, was compiled and submitted to CFDA Medical Device Registration Department. Mainly, the Medical Device Expert Roundtable (MDER) program I, II, III since Y2008, was described in the summary. Also, we recommend continue this EU-China cooperation program to have MDER IV, starting from this year.