Advocacy Actions
a 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.
Read moreLobby Letter to NMPA Commissioner on the Concerns and Suggestions from the Industry on Serious Delay of Registration of Special Cosmetics
Submitted lobby letter to NMPA Commissioner on the Concerns and Suggestions from the Industry on Serious Delay of Registration of Special Cosmetics.
Read moreSubmitted comments to MEE on 3 National Environmental Protection Standards for Technical Specifications for Application and Issuance of Pollution Discharge Permits
On 24 April, the European Chamber submitted comments to the Ministry of Ecology and Environment's 3 National Environmental Protection Standards for Technical Specifications for Application and Issuance of Pollution Discharge Permits.
Read moreMeeting with DDG Wei Li, Online Transaction Regulation Department, State Administration for Market Regulation (SAMR)
On 22nd April, European Chamber led a delegation to meet with Wei Li, Deputy Director-general of Department of Online Transaction Regulation, State Administration for Market Regulation (SAMR) and talked about the implement of E-commerce Law, supervision of online transaction and protection of consumer rights.
Read moreImplement smoothly the 1st review meeting with NMPA for a product, which secure the consequence that the European Chamber platform for reviewing innovative medical devices
Implement smoothly the 1st review meeting with NMPA for a product, which secure the consequence that the European Chamber platform for reviewing innovative medical devices.
Read moreComments to the MOT’s Mandatory National Standard for < Safety Requirements for Tanker Single Point Mooring Operation (Draft for Comments) >
The International Liner Shipping and Petrochemicals, Chemicals and Refining Working Groups submitted comments to the MOT's Mandatory National Standard for < Safety Requirements for Tanker Single Point Mooring Operation (Draft for Comments) >.
Meeting with National Medical Products Administration on the Administration of Medical Device Adverse Event Monitoring
On 18th April, the National Medical Products Administration (NMPA), along with National and Provincial Centers for Adverse Drug Reaction (ADR) Monitoring, held a meeting regarding the administration of Measures on Medical Device Adverse Event Monitoring, and the Guideline for Monitoring Adverse Events in particular.
Read moreJoint EUCCC and USITO WG meeting on Enterprise Standards
On 18th April, the European Chamber held a joint meeting with United States Information Technology Office (USITO) members on the topic of Enterprise Standards in Beijing.
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