Advocacy Actions
Comments to the Development and Reform Commission (DRC) of Guangdong Province on the draft "Examination and Approval of New and Revised Medical Service Prices"
The Healthcare Equipment Working Group submitted comments to the Development and Reform Commission (DRC) of Guangdong Province on the draft Examination and Approval of New and Revised Medical Service Prices
Read moreMeeting with the German Embassy on Waiving of Type Test Fees for Medical Devices
The Healthcare Equipment Working Group and COCIR met the Financial Counsellor of the German Embassy in Beijing to discuss options how to engage the Chinese Ministry of Finance regarding the question of Waiving of Type Test Fees for Medical Devices
Read moreMeeting with the European Delegation on Waiving of Type Test Fees and Regulatory Developments
The Healthcare Equipment Working Group and COCIR met officers of the European Delegation in Beijing to discuss options how to engage the Chinese Ministry of Finance regarding the question of waiving type test fees for medical devices and briefed the Delegation on latest developments in the regulatory environment for medical devices in China.
Read moreComments to CAC on Critical Information Infrastructure Protection Regulations
The European Chamber submitted collated comments on the Critical Information Infrastructure (CII) Protection Regulations to the Cyberspace Administration of China (CAC).
Read moreComments to the CMDE on "Guideline on Technical Evaluation of Registrations of Hepatitis C Virus Nucleic Acid Genotyping Reagents"
The Healthcare Equipment Working Group submitted comments to the CMDE's draft "Guideline on Technical Evaluation of Registrations of Hepatitis C Virus Nucleic Acid Genotyping Reagents"
Read moreMeeting with CFDA on reprocessing of single-use devices
Meeting with the Department of Medical Device Registration of the CFDA on reprocessing of single-use devices
Read moreComments to MIIT on <Compliance Management Catalogue of the Restriction of the Use of Hazardous Substances in Electrical and Electronic Products (First Batch)>
On 30th June, the Ministry of Industry and Information Technology (MIIT) issued a call-for-comments on the Compliance Management Catalogue of the Restriction of the Use of Hazardous Substances in Electrical and Electronic Products (First Batch) and Exempted list of the use of restricted substances of Compliance Management Catalogue. The European Chamber submitted the consolidated comments to the MIIT.
Read moreComments on CFDA's Draft "Administration of Developing Standards for Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments on the CFDA's Draft "Administration of Developing Standards for Medical Devices"
Read moreMeeting with New Director General of Center for Medical Device Evaluation, CFDA
HCE WG leadership met with New Director General of Center for Medical Device Evaluation, CFDA
Read moreComments to CFDA Draft Regulation on "Supervision of Online-sales of Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments to the CFDA's draft regulation on "supervision of online-sales of medical devices"
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