Advocacy Actions
Comments to NMPA's Public Consultation on the Techinal Guidelines for Clinical Evaluation Report for Medical Device Registration
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Techinal Guidelines for Clinical Evaluation Report for Medical Device Registration.
Read moreComments to NMPA's Public Consultation on the Technical Guidelines for Deciding Whether to Conduct Medical Devices Clinical Trails
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) on the Technical Guidelines for Deciding Whether to Conduct Medical Devices Clinical Trails.
Read moreComments to NMPA's Public Consultation on the Technical Guidelines for Medical Devices Equivalence Demonstration
The medical devices sector sent comments to the National Medical Producst Administration's (NMPA) public consultation on the Technical Guidelines for Medical Devices Equivalence Demonstration.
Read moreComments 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 moreEuropean Chamber staff meet with German Embassy Economic & Industry Counsellor
The counsellor of the German Embassy would like to know about the working groups' operation , lobby actions and plans. She is seeking for some common points and mutual support for the advocacy to protect the interest of German business
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 on Shenzhen HSA's Measures to Improve the Centralised Procurement of Medical Consumables
The Healthcare Equipment (HCE) Working Group submitted comments to Shenzhen Municipal Healthcare Security Administration's (Shenzhen HSA's) draft "Measures to Improve the Classified Centralised Procurement of Medical Consumables to Support Shenzhen’s Transparent Procurement Platform in Price Negotiations."
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 moreComments to the NHSA's National Volume Based Procurement of Joint Prostheses
The Healthcare Equipment (HCE) Working Group submitted comments to the National Healthcare Security's (NHSA's) "Concept for the National Volume Based Procurement of Joint Prostheses".
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