Advocacy Actions
Report 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.
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 the Chinese Academy of Sciences on Medical Technology Innovation and International Cooperation
On 18 February, the medical device sector met with the Chinese Academy of Sciences on medical technology and its innovation cooperation.
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 moreMeeting with CACE for Further Cooperation on Circular Economy
On 11th Jan, 2022, Jessica Yuan, Deputy Head of the government affairs department and June Yu, Business Manager of the government affairs visited Mr Zhao Kai, Vice President of China Association of Circular Economy.
Read moreComments submitted to National Medical Products Administration on Rules for the Implementation of the GB 9706.1-2020
Comments submitted to National Medical Products Administration on Rules for the Implementation of the GB 9706.1-2020
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