Advocacy Actions
Comments on “Guiding Principles for Registration and Technical Evaluation of Central Venous Catheters“
The Healthcare Equipment Working Group submitted Comments on the draft “Guiding Principles for Registration and Technical Evaluation of Central Venous Catheters“ to the Centre of Medical Device Evaluation (CMDE) of the CFDA.
Seminar: Theory and Practice of Punitive Compensation under Consumer Rights Protection Law
The Seminar was co-organised by CASS on Theory and Practice of Punitive Compensation under Consumer Rights Protection Law
Read moreInternational Labor Organization Officer Talks about Policy Implications on Employment Security Fund for Disabled People
On Nov 11, Mr. Haibin Zhou, the National Programme Officer for International Labor Office in China and Mongolia, presented policy implications on Employment Security Fund for Disabled People at European Chamber Beijing Office.
Read moreMeeting with Vice Mayor of Guiyang and President of Bank of China
On 10th October, European Chamber SME Advocacy Coordinator and Deputy Head of Government Affairs were invited by Bank of China, MIIT, NDRC and People's Government of Guizhou Province to participate in Cross-border Investment and Trade Fair, Guizhou Inland Opening-up Pilot Economic Zone Summit.
Read moreG20 Technology Innovation Forum
3rd of November, 2016, G20 Technology Innovation Minister Meeting was held in Beijing, the G20 Entrepreneur and Innovation Forum was organised by Ministry of Science and Technology, CCPIT, CCOIC at the same time.
Read moreMeeting with Pudong Market Supervision Bureau
Pudong is going to pilot the non-special imported cosmetics notification, which would be a milestone to realize the equal treatment of non-special imported cosmetic and non-special domestic cosmetics.
Read moreSeminar: Implementation Regulations of the law on the protection of consumer rights and Interests
The seminar was co-organized by Renmin University on Implementation Regulations of the law on the protection of consumer rights and Interests
Read moreMeeting with the Director of the Dept. for Innovation and Technology Policy, Ministry of Economic Affairs, Germany
The European Chamber briefed Dr Ole Janssen, Director of the Department for Innovation and Technology Policy, German Federal Ministry for Economic Affairs and Energy, on the opportunities and challenges of the Medical Device and Pharmaceutical Industry in China.
Read moreAAT Meeting with Department of Drug and Cosmetics Registration Management, CFDA
Chinese regulator, UK government representatives, experts of EU and China and EUCCC representative discussed the animal testing alternative methods verification and validation in China, the current progress and next step plan in the meeting.
Read moreComments on CFDA's "Adjustment of Risk Classification of IVD Reagents for Allergens"
The Healthcare Equipment Working Group submitted comments to the CFDA's draft "Adjustment of Risk Classification of IVD Reagents for Allergens".
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