Advocacy Actions
Comments to the MIIT and NHC’s Joint Public Consultation on the Provisions on High-end Medical Equipment Demonstration Zones Management (Trial) (Draft for Comments)
On 10 August, the Chamber sent comments to the Ministry of Industry and Information Technology and and National Health Commission’s Joint Public Consultation on the Provisions on High-end Medical Equipment Demonstration Zones Management (Trial) (Draft for Comments).
Read moreNMPA Seminar on Implementation of GB9706 series standards
Xu Jinghe, Deputy Commissioner of the National Medical Product Administration (NMPA) , organized a seminar on issues related to the implementation of the GB9706 series of standards, European Chamber was invited to attend and speak.
Read moreNMPA Seminar on Implementation of the Provision on Medical Device Registration
The National Medical Products Administration (NMPA) organised a seminar on the implementation of the Provision on Medical Device Registration, European Chamber was invited to attend and speak.
Read moreLetter to NMPA Giving Suggestions on Implementation of the Provision on Medical Device Registration
Letter to National Medical Products Administration Giving suggestions on Implementation of the Provision on Medical Devices Registration
Read moreMeeting with the Ministry of Finance on Government Procurement Issues
On 11 July, the delegation of the European Chamber met with the Ministry of Finance re government procurement issues.
Read moreEuropean 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.
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