Advocacy Actions
Comments to the CMDE to the draft Technical Review Guidelines for Human Factors in Design of Medical Devices
On 28 June, the medical device sector sent comments to Centre for Medical Device Evaluation on the draft Technical Review Guidelines for Human Factors in Design of Medical Devices.
Read moreAdvocacy Letter to the NMPA and the CMDE on Consequences of the Pending Medical Device Regulation (MDR) and In-vitro Diagnostic Medical Device Regulation (IVDR) in Europe for registrations in China
On 22 June, the medical device sector sent an advocacy letter to the National Medical Products Administration and the Centre for Medical Device Evaluation on consequences of the pending Medical Device Regulation (MDR) and In-vitro Diagnostic Medical Device Regulation (IVDR) in Europe for registrations in China.
Read moreCMDE published a Notice on filing acceptation（立卷审查) accepting comments we submitted
Center for Medical Device Evaluation of NMPA published a Notice on filing acceptation（立卷审查) accepting comments that we submitted
Read morePolicy Briefing on Yangshan Special Comprehensive Bonded Zone
Policy Briefing on Yangshan Special Comprehensive Bonded Zone
Read moreOfficial Interview: for 20th Anniversary
Official Iterview: for 20th Anniversary
Read moreMeeting with healthcare counsellors of Member States and the EU Delegation on market access affairs
Meeting with healthcare counsellors of Member States and the EU Delegation on market access affairs
Read moreComments to the Centre for Medical Device Evaluation on the Filing Review
On 25 May, the medical device sector submitted comments to the Centre for Medical Device Evaluation on the filing review as a fllow-up action of the meeting on 21 May.
Read moreMeeting with the Centre for Medical Device Evaluation on Filing Review
On 21 May, the medical device sector had a meeting with the Centre for Medical Device Evaluation had a meeting on the filing review.
Read moreContribute overview articles on Post-Market Surveillance in EU and UK to the Centre for Drug Re-evaluation
Contribute overview articles on Post-Market Surveillance in EU and UK to the Centre for Drug Re-evaluation
Read moreBriefing to COCIR Headquarter preparing for the Market Access Meeting organized by EC
Briefing to COCIR Headquarter preparing for the Market Access Meeting organized by EC
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