Advocacy Actions
COCIR Co-Organiser of the 8th China International Medical Device Regulatory Forum in Hangzhou
COCIR Co-Organiser of the 8th China International Medical Device Regulatory Forum in Hangzhou
Read moreComments 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 moreMeeting with AQSIQ on Combat Against Counterfeits and IPR Protection for Imports and Exports
On 14 August, 2017, the Chamber's representatives paid the visit to and had a dialogue with AQSIQ on anti-counterfeits and IPR protection for imports and exports.
Read moreLobby Action on Car Repair Certification Study requested by MOT
Ministry inquiry regarding Car Repair and Maintainance system in Germany and U.S. as well as U.K.
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 moreMeeting with Department of Economic Law of the NPCLAC
The Chamber had a meeting with Mr Yang Heqing, Deputy Director General of Department of Economic Law of the Legislative Affairs Commission of the National People’s Congress, NPCLAC.
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