Advocacy Actions
Comments to the National Healthcare Security Administration on the Draft "Nomenclature for Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments to the National Healthcare Security Administration's (NHSA's) draft "Medical Insurance ‘Nomenclature’ of Medical Consumable Devices".
Read more6th Technology Diplomats Innovation Resources Matchmaking Action
The Healtchare Equipment (HCE) Working Group participated in the 'Technology Diplomats Innovation Resources Matchmaking Action', organised by the Beijing Municipal Science & Technology Commission and the Beijing Technology Exchange & Promotion
Centre.
Comments to draft "Shandong, Shanxi, Hebei and Henan Volume-based Procurement Plan" for High-Value Consumable Medical Devices
The Healthcare Equipment (HCE) Working Group submitted comments to the Shandong Public Resources Trading Centre on the draft "Shandong, Shanxi, Hebei and Henan Volume-based Procurement Plan" for High-Value Consumable Medical Devices.
Read moreComments to Draft "Volume-based Procurement Plan for Intraocular Lenses in Beijing, Tianjin and Hebei"
The Healthcare Equipment (HCE) Working Group submitted comments to the Tianjin Healthcare Security Administration on the draft "Volume-based Procurement Plan for Intraocular Lenses in Beijing, Tianjin and Hebei".
Read moreGerman-Chinese Medical Industry Forum
Within the framework of the Medica Medical Technology Trade Fair, the China International Investment Promotion Agency (CIIPA) and the German Trade and Investment (GTAI) co-organised the German-Chinese Medical Industry Forum to promote bilateral promotion in healthcare.
Read moreAnnual Meeting of AI Medical Devices Standardization Technical Committee
Annual Meeting of AI Medical Devices Standardization Technical Committee
Read moreChamber Submitted Comments on the Draft Import and Export Inspection Credit-acceptance System
Chamber submitted comments on the draft Import and Export Inspection Credit-acceptance system
Read morelobby letter to National Medical Products Administration on Mandatory Standards Implementation
Lobby Letter to National Medical Products Administration on Mandatory Standards Implementation
Read moreMeeting the National Centre for Adverse Drug Reaction Monitoring
On 4 November, the medical sector had the meeting with the National Centre for Adverse Drug Reaction Monitoring re the medical device vigilance program.
Read moreComments to the "Technical Specification for National Procedures and Services in Medicine" of the Health Development Reseach Institute
The Healthcare Equipment and the Pharmaceuticals Working Group submitted comments to the draft "Technical Specification for National Procedures and Services in Medicine", prepared by the Health Development Reseach Institute under the National Health Commission (NHC).
Read more