Advocacy Actions
Meeting with Center for Drug Reevaluation CFDA
Round-table with CFDA Drug Re-evaluation Center on the development of the regulation - the Provision on Medical Device Adverse Events Monitoring and Re-evaluation
Read moreComments on Relevant Documents on Production Licence Reform
The Standards and Conformity Assessment (SCA) Working Group submitted comments on relevant documents on Production Licence Reform to the General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ).
Read moreComments to Draft "Purchasing Regulations on Purchasing of Disposable Medical Devices for General Surgery" in Zhejiang Province
The Health and Family Planning Commission (HFPC) of Zhejiang Province has formulated draft purchasing regulations specially for disposables used in general surgery.
The European Chamber's Consumable and Disposable Medical Devices (CDMD) Advisory Committee has formulated comments to the draft, focusing on several technical details of the regulations.
European Chamber Comments on CFDA Implementation Provision of Food Safety Law
European Chamber Comments on CFDA Implementation Provision of Food Safety Law
Read moreMeeting with Health and Family Planning Commission of Guangdong Province
A delegation of the CDMD Advisory Committee of the European Chamber met Mr. Wu Jingzheng, Director of the Department for Drug Policies of the Guangdong Provincial Health and Family Planning Committee, to discuss the recommendations of the European Chamber to the 2nd draft of the "Purchasing Regulations for Disposable Medical Devices"
Read moreMeeting with the CFDA
The representatives of the PN Desk met with the CFDA to discuss the registration of the infant and young children milk powder formula recipes and the registration of the FSMP.
Read moreLobby Letter to State Council Development and Reform Centre on Chinese Quality and Safety Conditions
A lobby letter on improving the poor quality and safety conditions in China by means of structural reforms was sent to Mr. Li Wei, President of the State Council Development and Research Centre, by the Quality and Safety Services Working Group.
Read moreComments to CFDA on the Provision on Medical Device Adverse Events Monitoring and Re-evaluation
European Chamber submitted comments to CFDA on the Provision on Medical Device Adverse Events Monitoring and Re-evaluation on 18th, Dec.
Read moreJoint Meeting with Beijing Municipal Government
Sara Marchetta, Vice President of the Chamber together with some members attended a joint meeting with the Vice Mayor of Beijing Municipal Government on the expansion pilots of opening up service sectors in Beijing.
Read moreMedia roundtable on Paris climate summit
In the meeting, Joerg Wuttke briefed the journalists on the European Chamber’s view on the Paris climate talks (COP21).
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