Advocacy Actions
Comments on the CFDA's draft "Rules of UDI System for Medical Devices
Industry comments on Rules of Unique Identification (UDI) System for Medical Devices were submit to CNDA in the name of EUCCC and COCIR
Read moreMeeting with Director of China Council for the Promotion of International Trade
Invited by China Council for the Promotion of International Trade, European chamber’s delegation met with CCPIT officials at their office to discuss issues regarding the potential impacts of the removal of JV restrictions for the auto sector in China.
Read moreComments on Measures for the Administration of Express Delivery Business Licensing
On Mar 28th, the State Post Bureau of The People’s Republic of China (SPB) issued the draft Measures for the Administration of Express Delivery Business Licensing for public consultation.
Read moreMeeting with FECO of MEE on the Market of Sludge Treatment in China
The European Chamber co-organsied the PIANO industry workshop on opportunities and challenges for European Business in the Market of Sludge Treatment in China
Read morePreparatory Meeting with CCFDIE for China International Medical Device Regulatory Forum (CIMDR)
The HCE Working Group met with the Centre for International Exchange of the CNDA (former CFDA) and industry delegates to prepare the 9th China International Medical Device Regulatory Forum (CIMDR) in September 2018
Read moreLobby Letter to General Administration of Customs on Clearance System Maintenance
The Logistics Working Group submitted a lobby letter to the General Administration of Customs with regards to the upgrading of the customs clearance system and the impact it brings for express delivery industry.
Read moreEuropean Chamber Speaks at the Shanghai Pujiang Intellectual Property International Forum
National Chair of the Intellectual Property Rights Working Group speaks at the Shanghai Pujiang Intellectual Property International Forum.
Read moreIMDRF Clinical Evaluation WG meeting - Subgroup 1
EUCCC-COCIR representative participated the International Medical Device Regulators Forum (IMDRF) Working Group meeting on Clinical Evaluation
Read moreMeeting with the EU Delegation on Market Access for Medical Devices
The Healthcare Equipment (HCE) Working Group of the European Chamber met with Mr Ruben Schellingerhout, Counsellor of the Trade Section of the Delegation of the European Union, on market access of medical devices.
Read moreMeeting with Counsellor of Swedish Embassy
Lotta Liljelund, the Counsellor of Economic Section and Head of CSR Centre and Madelene Trang, the Porgramme Officer, CSR Centre of Embassy of Sweden met with Ink Zheng, the business manager of CSR forum to discuss the sustainable trade development in China.
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