Advocacy Actions
Comments to the CMDE's draft "Technical Review Guideline for Modification of Registrations of IVD"
The Healthcare Equipment (HCE) Working Group submitted comments to the Centre of Medical Device Evaluation's (CMDE's) draft "Technical Review Guideline for Modification of Registrations of in-vitro diagnostics (IVD)".
Read moreRecommendations to Guangdong HSA's draft "Guideline on Promoting Group Procurement of Drug and Consumable Medical Devices"
The Healthcare Equipment Working Group submitted recommendations to the Guangdong Healthcare Security Administration's (HSA's) draft "Guideline on Promoting Group Procurement of Drug and Consumable Medical Devices".
Meeting with the Center for Medical Device Evaluation on the Technical Guideline on Examining the Function of Qualitative Testing Reagents (Draft for Public Consultation).
On 6th December, the Center for Medical Device Evaluation organized a meeting on the Technical Guideline on Examining the Function of Qualitative Testing Reagents (Draft for Public Consultation).
Read moreMeeting with the Center for Medical Device Evaluation on the Technical Review Guideline for Quantitative Testing Reagent Performance Assessment Registration (Draft for Public Consultation)
On 6th December, the Center for Medical Device organized a meeting on the Technical Review Guideline for Quantitative Testing Reagent Performance Assessment Registration (Draft for Public Consultation).
Read moreMeeting wiith DG Grow on Public Procurement in the Medical Device Industry
The Healthcare Equipment (HCE) Working Group and the Public Procurement Taskforce met with the Access to Procurement Markets Unit of DG GROW on challenges of European Companies in China's public market with a focus on the medical device market.
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 moreSeminar with the Health Security Administration of Jiangsu Province on Value-based Healthcare
A member company of the Consumable and Disposable Medical Device (CDMD) Advisory Committee of the Chamber organised a seminar with the Health Security Administration (HSA) of Jiangsu Province, municipial HSAs and provincial think tanks on value-based healthcare.
Read moreTraining for the Centre of Medical Device Evaluation (CMDE) on the EU Medical Device Regulation (MDR)
The Healthcare Equipment (HCE) Working Group gave a training for the Centre of Medical Device Evaluation (CMDE) on the EU Medical Device Regulation (MDR) and In-vitro Diagnostics Device Regulation (IVDR)
Read moreEU Member States Health Counselors Meeting on Pharmaceuticals
EU Member States Health Counselors Meeting on Pharmaceuticals
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.
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