Advocacy Actions
Meeting with the China Food and Drug Administration
On 3rd April, the representative of the PN Desk met with the CFDA to discuss the registration of formula.
Read moreComments to the "Principles for the Scope of Registration Certificates" Submitted to the CMDE
The Center of Medical Device Evaluation (CMDE) of the CFDA has asked for comments on the "Principles of the Scope of Registration Certificates". Based on the input of member companies, the HCE Working Group of the EUCCC in cooperation with COCIR has submitted their comments and recommendations to the CMDE.
Read moreMeeting with PRC Ministry of Commerce and State Council’s Legislative Affairs Office on Government Information Disclosure
On April 3rd, a delegation of the European Chamber led by Vice-President Mr. Bertrand de la Noue met with MofCom and the State Council’s Office of Open Government Information.
Read moreEUCCC Vice Chairman Meeting with SCOFCOM DG Shang Yuying
EUCCC Vice Chairman Meeting with SCOFCOM DG Shang Yuying
Read moreMeeting with China Desk of DG Energy of the European Commission
Representatives from the Chamber met with Ms. Eva De Bleeker from DG Energy's China Desk of the European Commission to find out how the European Commission’s energy dialogue with China could better support European companies.
Read moreMeeting with German Consul on Foreign School’s Operation in Shanghai
Meeting with German Consul on Foreign School’s Operation in Shanghai
Read moreMeeting with the EU Delegation (DG SANTE) on eHealth Roundtable with NHFPC
The EU Delegation (DG SANTE), COCIR and EUCTP discussed the backgroud, status and actions moving forward, on the eHealth Expert Roundtable, which industry is trying to have with NHFPC
Read moreMeeting with Department of Medical Device Supervision of the CFDA on actual issues on post-market surveillance
A Meeting of delegates of European and American Company Delegates on Actual Issues related to Post-Market Surveillance
Read moreCFDA Call for Comments on Issue of Export Certificates for Medical Devices
Comments on the CFDA's Draft of the < Administration Rules for the Issue of Export Certificates for Medical Devices >