Advocacy Actions
Seminar on Commodity Inspection of Medical Device with Shanghai Customs
On 1st November, the medical device organized a seminar on the commodity inspection of medical device and invited one official from the Shanghai Customs as speaker.
Read moreComments to the State Administration of Market Regulation on Administrative Measures for the Examination of Advertisements for Medicine, Medical Device, Health Food and FSMPs(Draft for Comments)
Following the State Administration for Market Regulation initiated the third round public consultation on Administrative Measures for the Examination of Advertisements for Medicine, Medical Device, Health Food and FSMPs(Draft for Comments), the European Chamber has collated all member inputs and submitted them to the SAMR upon circulation of the draft within relevant working groups.
Read moreComments to the CMDE's Draft Clinical Evidence Section of eRPS
On 31st October, the medical device sector submitted comments on the draft Clinical Evidence Section of eRPS.
Read moreReference of Low-hanging Fruit for Medical Device Sector
On 23rd October, the medical device sector provided the low-hanging fruit list to the Delegation of the European Union to China.
Read moreMeeting with the Shaanxi Provincial Health Security Administration on Procurement of Disposable Medical Devices
The Healthcare Equipment (HCE) Working Group hold a meeting with the Shaanxi Provincial Health Security Administration (HSA) on procurement of disposable medical devices.
Read more“Rule of Law is the Best Business Environment”: President Wuttke and Working Group Representatives Meet with NPCLAC Vice Chairman Liu Junchen
On 18th October, European Chamber President Jörg Wuttke and representatives from the Legal and Competition, Information and Communication Technology, Healthcare Equipment, and Automotive working groups, Cybersecurity Sub-working Group, Paediatric Nutrition Advisory Committee and the Fashion and the Leather Advisory Committee met with Liu Junchen, vice chair, Legislative Affairs Commission, Standing Committee of the National People's Congress (NPALAC).
Read moreComments to the CMDE’s 'Technical Guideline on Examining the Function of Qualitative Testing Reagents (Draft for Public Consultation)'
On 25th September, the Center for Medical Device Evaluation initiated the public consultation on the Technical Guideline on Examining the Function of Qualitative Testing Reagents (Draft for Public Consultation).
Read moreMeeting with ETSI representatives
On 16th October, representatives from the Standards and Conformity Assessment, Healthcare Equipment and Information and Communication Technology Working Groups met with a delegation from the European Telecommunications Standards Institute (ETSI).
Read moreAdvocacy Letter to the Ministry of Finance and the Ministry of Commerce on Buy China Issues
On 15th October, the medical device sector sent two advocacy letter to the Ministry of Finance and the Ministry of Commerce on Buy China issue.
Read moreComments to the CMDE's Public Consultation on the Technical Review Guideline for Quantitative Testing Reagent Performance Assessment Registration
On 10th October, the medical devices sector submitted comments to the Centre for Medical Device Evaluation's (CMDE) Public Consultation on the Technical Reneview Guideline for Quantitative Testing Reagent Performance Assessment Registration.
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