Advocacy Actions
Plenary Meeting with CMDSA on the Standard of Energy Consumption of Medical Equipment
Plenary Meeting on the Standard of Energy Consumption of Medical Equipment
Read moreAttended the Artificial Intelligence Medical Device Innovation and Cooperation Platform
On 27 December, COCIR Representative and several member companies attended the Artificial Intelligence Medical Device Innovation and Cooperation Platform.
Read moreComments to the CMDE's Public Consultation on the Guideline on Supplementary Materials for Medical Equipment Registration and Assessment (Draft for Comments)
On 26th November, the medical device submitted comments to the Center for Medical Device Evaluation on it s public consultation on the Guideline on Supplementary Materials for Medical Equipment Registration and Assessment (Draft for Comments).
Read moreMeeting with DG Trade on "Buy China" Issue
Using the opportunity of a face to face meeting with Trade Officer in Brussels, highlighted the "Buy China" policy issue in Guangxi
Read moreEU Member States Health Counselors Meeting on Pharmaceuticals
EU Member States Health Counselors Meeting on Pharmaceuticals
Read moreDeliver industry voice during COCIR 60 Years Anniversary event to the European Commission
During COCIR 60 Years Anniversary event, industry voices were raised to the European Commission and other stakeholders.
Read moreSpeech at National Experience Exchange Meeting on Quality Management System of Medical Devices Organized by NMPA
On 8th November, the Chamber was invited to attend the National Experience Exchange Meeting on Quality Management System of Medical Devices organized by the National Medical Products Administration.
Read moreSeminar on Commodity Inspection of Medical Device with Shanghai Customs
On 1st November, the medical device organized a seminar on the commodity inspection of medical device and invited one official from the Shanghai Customs as speaker.
Read moreComments to the State Administration of Market Regulation on Administrative Measures for the Examination of Advertisements for Medicine, Medical Device, Health Food and FSMPs(Draft for Comments)
Following the State Administration for Market Regulation initiated the third round public consultation on Administrative Measures for the Examination of Advertisements for Medicine, Medical Device, Health Food and FSMPs(Draft for Comments), the European Chamber has collated all member inputs and submitted them to the SAMR upon circulation of the draft within relevant working groups.
Read moreComments to the CMDE's Draft Clinical Evidence Section of eRPS
On 31st October, the medical device sector submitted comments on the draft Clinical Evidence Section of eRPS.
Read more