Advocacy Actions
Online Meeting with SAMR and CNIPA on Intellectual Property Issues
On Monday, 21st December, European Chamber IPR working group chairs Mr Filippo Sticconi, Mr Reinout van Malenstein, and Mr Yajun Bai met with the delegation of officials from the State Administration for Market Regulation (SAMR) and the China National Intellectual Property Administration (CNIPA) to discuss IP concerns share by member companies. Together online are representatives from the EU Delegation Trade Office Ms Helene Juramy and Ms Liu Qi.
Read moreMeeting with Ministry of Industry and Information Technology
Introduction of EUCCC and members of Aviation & Aerospace WG to MIIT , division II, and both sides expressed willing to strengthen the cooperation.
Read moreRecommendation on Shandong Government Procurement Centre's Draft Document "Volume-based Centralised Procurement of High Value Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments to the Shandong Government Procurement Centre's draft document "Volume-based Centralised Procurement of High Value Medical Devices".
Read moreMeeting with the Centre of Medical Device Evaluation on Innovative Medical Device Registration
On 16 December, the Chamber attended the Innovative Medical Device Registration Meeting held by the Centre for Medical Device Evaluation.
Read moreMeeting with Environment center of Ministry of Ecology and Environment
Vice DG of the Center, MEE and EUCCC representatives did the introductions receptively and discussed about potential exchanges and cooperation.
Read moreWorkshop on Green and Circular Economy in China
The workshop provides an overview of the green and circular economy sector in China, its priorities for the 14th Five-year Plan period and the main challenges that European companies face in the industrial sectors.
Read moreSAMR Seminar on the Revision of Secondary Documents of Administrative Measures for Infant Formula Registration
On December 15th, representatives of Paediatric Nutrition Desk participant the meeting organized by the Special Food Administration and Supervision Department, State Administration for Market Regulation, on the revision of secondary documents of Administrative Measures for Infant Formula Registration.
Read moreComments on CMDE’s Public Consultation on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents (Draft for Comments)
On 15 December, the medical device sector submitted the comments on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents (Draft for Comments) published by the Centre for Medical Device Evaluation.
Read moreComments on the NMPA’s Public Consultation on the Dynamical Adjustment Working Procedure of Medical Device Classification Catalog (Draft for Comments)
On 15 December, the medical device sector sent comments on the Dynamical Adjustment Working Procedure of Medical Device Classification Catalog (Draft for Comments) released by the National Medical Products Administrtaion for public consultation.
Read moreMeeting with National Healthcare Security Administration on Cooperation in 2021
Meeting with National Healthcare Security Administration on Cooperation in 2021
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