Advocacy Actions
Exclusive Dialogue with SAIC on the New Advertising Law
On July 14, an Exclusive Dialogue with Deputy Director General Huang Xinmin, Department of Advertisement Supervision and Management, State Administration for Industry and Commerce, on the new Advertisement Law was held.
Read moreSpeaking opportunity at the EU-China Business Summit and participation at CEO Lunch
President Joerg Wuttke delivered a speech at the business leaders’ plenary session of the EU-China Business Summit which took place in Brussels on the 29th June, 2015.
Read moreSpeaking opportunity at the 2nd Innovation Cooperation Dialogue
Mr. Bruno Gensburger, State Representative at ExCo delivered a speech during the 2nd Innovation Cooperation under the session on innovation framework conditions.
Read more中国欧盟商会关于《政府核准和备案投资项目管理条例》(征求意见稿)》反馈意见
European Chamber Comments on Regulation on Government Approval and Filing of Investment Projects (Draft for Comments)
Read more中国欧盟商会关于《中华人民共和国国家安全法(草案)(二次审议稿)》的意见
European Chamber Comments on: PRC National Security Law (Second Reading Draft)
Read moreProvide a briefing to EUD on "Buy China" Initiatives issue
Provide a briefing to EUD on "Buy China" Initiatives issue
Read moreMeeting with CCFDIE on China International Medical Device Regulatory (CIMDR) Forum
COCIR was invited by China Center for Food and Drug International Exchange (CCFDIE) of CFDA for the kick-off meeting for CIMDR VI in Y2015, especially for the Medical Imaging sub-forum.
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 >