Advocacy Actions
European Chamber Comments on The Verification Guide for Medical Device Registration Quality Management System (Revised Draft for Comments)
The European Chamber submitted the members’ Comments on The Verification Guide for Medical Device Registration Quality Management System (Revised Draft for Comments) on 24th June.
Read moreComments to the NMPA: Publicly solicit opinions on the "Opinions on Strengthening the Grading Supervision of the Production and Operation of Medical Devices (Draft for Solicitation of Comment)
The European Chamber submitted comments to the NMPA on Publicly solicit opinions on the "Opinions on Strengthening the Grading Supervision of the Production and Operation of Medical Devices (Draft for Solicitation of Comment)".
Read moreEU-China Seminar on Green and Low-carbon Transition and Technology Exchange
On 10th June, the Environment working group of the European Chamber and the Foreign Environmental Cooperation Center (FECO) of the Ministry of Ecology and Environment (MEE) co-organised an online seminar on green and low-carbon transition and technology exchange. The seminar was focused on the China-EU Green and Low-Carbon Transformation Technology Exchange and Sharing and the Urban Low-carbon Transformation Path.
Read moreMeeting the National Centre for Adverse Drug Reaction (ADR) Monitoring
Meeting the National Centre for Adverse Drug Reaction (ADR) Monitoring
Read moreComments to MOST on the Implementing Rules of the Regulations for the Administration of Human Genetic Resources
On 21 April, the European Chamber submitted comments to the Ministry of Science and Technology on the Implementing Rules of the Regulations for the Administration of Human Genetic Resources.
Read moreReport submitted to the National Medical Products Administration (NMPA) on medical device classification
The European Chamber is invited by NMPA to study the difference on classification of medical device between the Europe and China.
Read moreMeeting with Centre for Medical Device Evaluation on Compliance during Registration Application
Meeting with Centre for Medical Device Evaluation on Compliance during Registration Application
Read moreEuropean Chamber Third Medical Device Forum
On 24 March 2022, the medical device sector of the European Chamber in cooperation with the European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry (COCIR) hosted the annual medical device forum.
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.