Advocacy Actions
Meeting with CFDA Medical Device Supervision Department and Privincial FDA on Administration Rules for the Issue of Export Certificates for Medical Devices
As the only foreign Chamber of Commerce, EUCCC was invited by CFDA Medical Device Supervision Dept. (MDSD) for a seminar with CFDA MDSD, provincial FDA, China Association for Medical Device Industry (CAMDI), some domestic companies and 2 foreign companies, discussing about the draft Administration Rules for the Issue of Export Certificates for Medical Devices.
Read moreMeeting with EC DG Trade preparing for the ETWG meeting
Meeting with EC DG Trade head and officers from Brussels and Delegation in China to prepare their meeting with Chinese authorities, the EU-China Economic & Trade Working Group (ETWG) Meeting 6-7th May, 2015 in Beijing
Read moreMeeting with NDRC and CFDA on Regulations for Registration Fee of Pharmaceuticals and Medical Devices that is in drafting
Roundtable with NDRC and CFDA on Medical Device Registration Fee to be charged
Read moreMeeting with the CFDA on Registration Fees for Medical Devices
A delegation of the HCE Working Group of the EUCCC visited the CFDA and exchanged opinions about the planned registration fees for medical devices.
Read moreComments on "Requirements to Registration Dossier for Medical Software" submitted to CMDE
The Center of Medical Device Evaluation (CMDE) of the CFDA had issued a Call for Comments on the Requirements to the Registration Dossier for Medical Software. Based on the input from member companies the EUCCC had submitted consolidated comments and suggestions to the CMDE
Read moreComments to the "Principles for the Scope of Registration Certificates" Submitted to the CMDE
The Center of Medical Device Evaluation (CMDE) of the CFDA has asked for comments on the "Principles of the Scope of Registration Certificates". Based on the input of member companies, the HCE Working Group of the EUCCC in cooperation with COCIR has submitted their comments and recommendations to the CMDE.
Read moreMeeting with Department of Medical Device Supervision of the CFDA on actual issues on post-market surveillance
A Meeting of delegates of European and American Company Delegates on Actual Issues related to Post-Market Surveillance
Read moreCFDA Call for Comments on Issue of Export Certificates for Medical Devices
Comments on the CFDA's Draft of the < Administration Rules for the Issue of Export Certificates for Medical Devices >
CFDA: Provisions on "Qualification of Medical Institutions to Conduct Clinical Trials"
Draft Regulations by the CFDA which conditions hospitals (or equivalent medical institutions) must fulfill to be qualified to conduct clinical trials for medical devices.
Read moreMeeting with China Association of Medical Equipment (CAME)
COCIR, MITA and CAME exchanged opinions about delelopmtent of the Medical Imaging Industry as well as "Buy China" Initatives of the NHFPC.
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