Advocacy Actions
European Chamber President meets with Joanna Szychowska, Director at DG TRADE
On 15th April, a delegation of European Chamber representatives led by President Jens Eskelund met with Joanna Szychowska, Director at DG TRADE, and other visiting officials.
Read moreMeeting with State Administration for Market Regulation
On 19th January 2024, the European Union Chamber of Commerce in China participated a roundtable discussion on continuously optimizing business environment and facilitating high quality development at the State Administration of Market Regulation (SAMR).
Read moreHigh-End Medical Equipment Recycling and Remanufacturing Private Seminar
Discuss the model of recycling and remanufacturing of high-end medical equipment, and the decarbonization targets and related policies in China and EU.
Read moreCOCIR Environment & Remanufacturing Focus Group Annual Meeting
High-end medical equipment recycling and remanufacturing model discussion.
NMPA Mandatory Standard & RA Policy Meeting with Industrial Organizations
To discuss issues related to the implementation of mandatory standards for medical devices.
Read moreMeeting with CMDE on Mandatory Standard Implementation Issue
CMDE met with representatives of relevant industry associations on evaluation policy after the implementation of mandatory standards.
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Read moreSubmit Comments/Recommendations to CFDA on the Draft Guidance for Medical Software Evaluation
Submit Comments/Recommendations to CFDA on the Draft Guidance for Medical Software Evaluation
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