Advocacy Actions
Comments to NMPA's Public Consultation on the Technical Guideline for Medical Devices Clinical Evaluation
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Technical Guideline for Medical Devices Clinical Evaluation.
Read moreComments to NMPA's Public Consultation on the Technical Guidelines for In Vitro Diagnostic Clinical Trials
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Technical Guidelines for In Vitro Diagnostic Clinical Trials.
Read moreMeeting with the CCFDIE to Support 12th CIMDR
On 10 May, the medical device sector met with the China Centre for Food and Drug Internation Exchange to discuss the preparation for the China Internation Medical Device Regulatory Forum (CIMDR) this year.
Read moreComments to NMPA on the Administration Measures for Supervision of Medical Device Manufacturing (Revised Draft for Comments)
On 25 April, the medical device sector sent comments to the National Medical Products Administrtaion on the Administration Measures for Supervision of Medical Device Manufacturing (Revised Draft for Comments).
Read moreMeeting with European Counsellors on Medical Devices
Meeting with European Counsellors on Medical Devices
Read moreUpdate Key Barriers List for medical device sector
Update Key Barriers List for medical device sector
Read moreComments on NHC’s Public Consultation on the Measures for the Ethical Review of Life Science and Medical Research Involving Humans (Draft for Comments)
On 14 April, the medical device sector sent comments to the National Health Commission’s (NHC) Public Consultation on the Measures for the Ethical Review of Life Science and Medical Research Involving Humans (Draft for Comments).
Read moreComments on the NMPA’s Public Consultation on the Emergency Approval Procedures for Medical Devices (Revised Draft for Comments)
On 14 April, the medical medvice sector sent comments to the National Medical Products Administration’s (NMPA) Public Consultation on the Emergency Approval Procedures for Medical Devices (Revised Draft for Comments).
Read moreMeeting with the Embassy of the Netherlands on Cooperation in the Field of Healthcare
The Healthcare Equipment (HCE) Working Group and COCIR China met with the newly appointed counselor for health, welfare and sport on cooperation in the field of healthcare.
Read moreComments on the MIIT’s Public Consultation on the Medical Equipment Industry Development Plan (2021-2025) (Draft for Comments)
On 11 March, the medical device sector submitted comments on the Ministry of Industry and Information Technology’s public consultation on the Medical Equipment Industry Development Plan (2021-2025) (Draft for Comments).
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