Advocacy Actions
Comments to Sichuan HSA's draft 'Reforming the Administration of High-value Consumables'
The Healthcare Equipment (HCE) Working Group submitted comments to the Sichuan Healthcare Security Administration's (Sichuan HSA's) draft document 'Reforming the Administration of High-value Consumable Medical Devices in Sichuan Province'.
Read more2020 Foreign Experts Symposium Organised by MOST
A delegate of the European Chamber was invited to participate in the annual Foreign Experts Symposium. The symposium, organised by the Ministry of Science and Technology (MOST) serves as a forum for international experts to bring forward recommendations how to further boost science and technology in China.
Read moreComments to the CMDE’s Public Consultation: Technical Guidelines on Medical Device Clinical Evaluation
On 16th January, the medical device sector submitted comments to the Center for Medical Device Evaluation on its public consultation on the Technical Guidelines on Medical Device Clinical Evaluation.
Read moreFeedback to the EUD Survey on Opening up of China's Healthcare Market
The Healthcare Equipment (HCE) Working Group provided feedback on the European Union Delegation's (EUD's) survey on the effect of China's continuing opening up of the healthcare market.
Read moreupdate the key market access barrier list for China, for medical device sector
key barriers list China for medical device sector is updated for Y2020
Read moreComments to the MIIT's Application for the Preparation of the National Technical Committee for the Standardization of Medical Equipment
On 3rd January, the medical device sector submitted comments to the Ministry of Industry and Information Technology 's Application for the Preparation of the National Technical Committee for the Standardization of Medical Equipment.
Read moreAttended 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.
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