Advocacy Actions
5th China Medical Device Vigilance Conference
The 5th China Medical Device Vigilance Conference was held on 2 December.
Read moreAdvocacy Letter to the State Administration for Market Regulation on Medical Devices Remote Inspection During COVID-19
On 25 November, the medial device sector submitted an advocacy letter to the State Administration for Market Regulation on medical devices remote inspection during COVID-19.
Read moreEuropean Chamber South China Chapter Meets with the Guangdong Provincial Heatlh Commission to Discuss the "Buy China" Issue
The European Chamber South China Chapter attended a meeting with the Guangdong Provincial Health Commission to discuss the concerns surrounding Guangdong Province's policy encouraging hospitals to buy domestic medical products over foreign medical products.
Read more11th China Medical Device Regulatory Forum (CIMDR)
The China International Medical Device Regulatory Forum (CIMDR), an annual event to bring the China National Medical Product Administration (NMPA), international regulators and Regulatory Affairs (RA) experts of medical device manufacturers together, to discuss and harmonise regulatory developments in China and the world, took place from 18. - 20. November in Fuzhou. About 1600 delegates participated.
Read moreMeeting with Fujian Healthcare Security Administration on Procurement of Disposable Medical Devices
The Healthcare Equipment (HCE) Working Group hold a meeting with the Fujian Healthcare Security Administration (HSA) on procurement of disposable medical devices
Read moreMeeting with the Centre for Medical Device Evaluation on the Technical Review Guideline for Change of Administrative Licensing Items of In Vitro Diagnostic Reagents (Draft)
On 16th November, the Chamber had a meeting with the Centre for Medical Device Evaluation on the Technical Review Guideline for Change of Administrative Licensing Items of In Vitro Diagnostic Reagents (Draft).
Read moreComments on the NMPA's Public Consultation on the National Medical Device Quality Sampling Inspection Work Procedure (Draft for Comments)
On 12th November, the medical device sector submitted comments on the National Medical Device Quality Sampling Inspection Work Procedure (Draft for Comments) to the National Medical Products Administration.
Read moreAdvocacy Letter on Medical Device Registration Confidentiality Issues
On 06 November, the medical device sector sent an advocacy letter to the National Medical Products Administration on the medical device registration confidentiality issues.
Read morePresident Wuttke Presented Position Paper to Development Research Centre of the State Council (DRC)
A delegation led by President Wuttke, including Shipbuilding Working Group (WG), Pharma WG, HCE WG, Energy WG, Environment WG, Automotive WG, ILS sub WG, and PN Desk held a high-level meeting with Development Research Centre of the State Council to present the Chamber's 2020/2021 Position Paper.
Read moreRoundtable with MOFCOM Official on European Business Operations in China
Roundtable with MOFCOM Official on European Business Operations in China
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