Advocacy Actions
Meeting with Deputy Director Yang Ting, Department of Development Research, China Council for the Promotion of International Trade (CCPIT)
On 23rd May, Chamber’s government relations manager Michelle Zhang led the delegation from the European Chamber to meet with Mr. Yang Ting, Deputy Director of the Department of Development Research, China Council for the Promotion of International Trade (CCPIT). Member representatives of the Automotive, Healthcare Equipment (HCE), Aviation & Aerospace (A&A), GA Forum and the Advisory Council attended the meeting. Michelle presented the Chamber’s newly published Business Confidence Survey 2019 to the Deputy Director.
Read moreComments to the European Commission on the Investment Restrictions on the Medical Device Sector in China
On 21st May, the medical sector submitted comments to the European Chamber regarding the investment restrictions on the medical device sector in China.
Read moreEUCCC Innovation Centre–Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-Off
On 17th May 2019, the European Chamber and the Centre for Medical Devices Evaluation (CMDE) of the National Medical Products Administration (NMPA), co-organized the Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-off.
Read moreComments to State Administration of Market Regulation (SAMR) on Administrative Provisions on Product Quality Supervision and Spot Inspections (Draft for Comments)
The European Chamber's Automotive, HCE, SCA, Fashion and Leather, Cheese and other working groups jointly submitted comments to the SAMR on the Administrative Provisions on Product Quality Supervision and Spot Inspections (Draft for Comments).
Read moreMeeting with the NIFDC on Cooperation in the field of Blood Screening
The Healthcare Equipment (HCE) Working Group met with representatives of the National Institutes for Food and Drug Control (NIFDC), the National Medical Products Administration (NMPA), the National Health Commission (NHC) and the World Health Organisation (WHO) on cooperation in the field of blood screening.
Read moreContribute to the "Green Book" of Medical Devices in China
Contribute to the "Green Book" of Medical Devices in China
Read morefeedback to the EU Delegation for questions regarding biotechnology
Feedback to the EU Delegation for questions regarding biotechnology
Read morea Report on Medical Device Standards was Submitted to NMPA
HCE-COCIR was approached by NMPA for a report on medical device standards. Upon industry experts' advice, a report was submitted to Center for Medical Device Evaluation of NMPA.
Read moreSubmitted Comments to the Centre for Medical Device Evaluation on the draft Criteria for Establishing a Registration Project.
On 12th April 2019, the Centre for Medical Device Evaluation (CMDE) has initiated public consultations on the draft Criteria for Establishing a Registration Project.
Read morePreparatory Meeting for the 10th China International Medical Device Regulatory Forum
On the 24th April, the China Center for Food and Drug International Exchange and the Center for Medical Device Evaluation of the National Medical Products Administration held a preparatory meeting for the 10th China International Medical Device Regulatory Forum.
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