Advocacy Actions
Comments on NIFDC’s Public Consultation on the Health Software Part1 General Requirements for Product Safety
The medical device sector submitted comments on the Centre for Medical Device Standardization Administration’s Public Consultation on the Health Software Part1 General Requirements for Product Safety.
Read moreMeeting with Experts and Officials from the Beijing Pilot Program on Cross-border Data Flow working group
The European Chamber company representatives met with experts and officials from the Beijing Pilot Program on Cross-border Data Flow Working Group for a seminar on the development of the pilot program and the application channels.
Read moreCOCIR Refurbishment Group Annual Meeting, Inviting CACE and WEF Give Presentations
COCIR Refurbishment Group Annual Meeting, Inviting CACE and WEF Give Presentations
Read moreBriefing to COCIR Headquarter preparing for the meeting of Market Access WG for Medical Devices organized by DG Trade in Brussels
Briefing to COCIR Headquarter preparing for the meeting of Market Access WG for Medical Devices organized by DG Trade in Brussels
Read moreComments to CCCMHPIE on Issues Faced by Enterprises During Port Customs Clearance
On 03 February, the medical device sector sents comments to the China Chamber of Commerce for Import and Export of Medicines and Health Products (CCCMHPIE) on issue faced by enterprises during port Customs clearance.
Read moreFollow-up Advocacy Letter to the CMDE on the Guidelines for Registration and Declaration of the Shelf Life Time of Passive Implantable Medical Device
On 29 January, the medical device sent a follow-up advocacy letter to the Centre for Medical Device Evaluation on the Guidelines for Registration and Declaration of the Shelf Life Time of Passive Implantable Medical Device.
Read moreFacilitate the Consultation from the CMDE to the EC regarding Guidelines of the EC for Medical Devices
Facilitate the Consultation from the Center for Medical Device Evaluation to the European Commission with regards to Information about Guidelines of the EC for Medical Devices
Read moreComments on NMPA’s Public Consultation on the Opinions on Further Strengthen Medical Device Standardization (Draft for Comments)
On 15 January, the medical device sector sent comments on the Opinions on Further Strengthen Medical Device Standardization (Draft for Comments) published by the National Medical Products Administration for public consultation.
Read moreAdvocacy Letter to CMDE on Registration Issues Encountered by Enterprises
On 15 January, the medical device sector sent an advocacy letter to the Centre for Medical Device Evaluation on recent registration issues encountered by enterprises.
Read moreMeeting with NMPA and Hainan MPA on Regulatory Science Research
Meeting with the NMPA and Hainan local MPA on the work of the Regulatory Science Research Institute in Hainan
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