Advocacy Actions
Attended the Artificial Intelligence Medical Device Innovation and Cooperation Platform
On 27 December, COCIR Representative and several member companies attended the Artificial Intelligence Medical Device Innovation and Cooperation Platform.
Read moreFollow-up Advocacy Letter to the National Medical Products Administration on the Registration and Administration of Blood Screening IVD Products
On 23rd December, the medical devices sector submitted an advocacy letter to the National Medical Products Administration on the registration and administration of blood screening In Vitro Diagnosis products as the follow-up action of the advocacy letter sent on 19th September.
Read moreComments to the NDRC's Draft 'Ammendment of the Tender Law'
The Public Procurement Taskforce submitted comments to the National Development and Reform Commission's (NDRC's) draft 'Amendment to Tender Law of the PR China'.
Read moreSurvey on access to standardisation activities
From 2nd to 12th December, the Standards and Conformity Assessment Working Group, along with other relevant Working Groups, launched a survey to better understand the issues with access to standardisation activities of European businesses.
Read moreComments 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).
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