Advocacy Actions
Meeting with Import and Export Food Safety Bureau, AQSIQ
On April 30th , European Chamber delegation led by Vice President Juliette Song attended a meeting with Bai Lu, the DDG of Import and Export Food safety Bureau, AQSIQ, discussing the issue of implementation of a track record management system.
Read moreParticipation in panel discussion at the 8th China Urbanisation International Summit
A representative of the Chamber was invited as a panelist at the 8th China Urbanisation International Summit
Read moreProvide a briefing to EUD on "Buy China" Initiatives issue
Provide a briefing to EUD on "Buy China" Initiatives issue
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 CCFDIE on China International Medical Device Regulatory (CIMDR) Forum
COCIR was invited by China Center for Food and Drug International Exchange (CCFDIE) of CFDA for the kick-off meeting for CIMDR VI in Y2015, especially for the Medical Imaging sub-forum.
Read moreRenewable Energy Working Group Meeting to discuss the Position Paper
The Deputy Director of the think tank Policy Research Center for Environment and Economy was invited to analyse and discuss the Renewable Energy Position Paper
Read moreLobby Letter to the Commission of Legislative Affairs Standing Committee of the National People’s Congress (NPC)
On 17th April, the PN Desk submitted a lobby letter to the Commission of Legislative Standing Committee of the NPC regarding the industry concerns on the Advertisement Law.
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 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
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