Advocacy Actions
Meeting 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 moreSpeaking opportunity at NDRC – CCUD China International Urbanisation Forum 2015
A representative from the Chamber was invited as a speaker during the NDRC – CCUD China International Urbanisation Forum 2015
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 moreMeeting with China Association of Development Zones (CADZ)
Representatives from the Chamber met with representatives of the Association of Development Zones regarding potential events
Meeting with think tank Policy Research Center for Environment and Economy under the Ministry of Environmental Protection
Meeting with think tank Policy Research Center for Environment and Economy under the Ministry of Environmental Protection
Read moreMeeting with the China Food and Drug Administration
On 10th April, the representative of the PN Desk met with the CFDA to discuss the Food for Special Medical Purpose(FSMP).
Read moreEuropean Chamber Beijing Local Position Paper Launch Eventand Press Conference
The European Chamber launched its Beijing Local Position Paper on April 9 2015
Read moreMeeting with Chairs and Vice-Chairs of the European Parliament’s Delegation for Relations with the People’s Republic of China
The European Chamber met with the Chairs and Vice-Chairs of the European Parliament’s Delegation for Relations with the People’s Republic of China. This visit from is part of preparations for the upcoming MEP visit to China in July; results from this trip will be carried back to the foreign policy committee at the European Parliament. This meeting was also an opportunity to relay the needs of European businesses in China and reflect on how the CAI might be helpful for further establishing European business across China.
Read moreMeeting with the China Food and Drug Administration
On 3rd April, the representative of the PN Desk met with the CFDA to discuss the registration of formula.
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.
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