Advocacy Actions
Comments to NMPA’s Public Consultation: Catalogue of Medical Device Prohibited to Entrusted Manufacturing (Draft for Comments)
On 15 December, the medical device sector sent comments to the National Medical Products Admisnitration’s Public Consultation: Catalogue of Medical Device Prohibited to Entrusted Manufacturing (Draft for Comments).
Read moreComments to NIFDC's Public Consultation on the Medical Device Classification Catalogue (Call for Comments)
On 9 December, the medical devices sector sent comments to the Centre for Medical Device Standardisation Administration (NIFDC) on the Medical Device Classification Catalogue (Call for Comments).
Read moreMeeting with Mr. Ramunas Freigofas, First Counsellor for Health and Food Safety of EU Delegation to China
European Chamber representatives from agriculture, EU affairs, food and beverage, cosmetics, healthcare equipment, pharmaceutical sectors, met with Mr. Ramunas Freigofas, First Counsellor for Health and Food Safety of EU Delegation to China to exchange work priorities of both sides and plan for further cooperation.
Read moreAnnual Meeting of AI Medical Devices Standardization Technical Committee
Annual Meeting of AI Medical Devices Standardization Technical Committee
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 moreWorkshop with the Centre for Medical Device Evaluation on Guideline for Clinical Data Submission
The Healthcare Equipment (HCE) Working Group and COCIR participated in workshop organised by the Centre of Medical Device Evaluation (CMDE) on the draft Guideline for Clinical Data Submission.
Read moreComments to CMDE’s Public Consultation: Guidelines on the Medical Device Product Technical Requirements Compilation Registration Review (2021 Revision) (Draft for Comments)
On 8 October, the medical device sector sent comments to the Centre for Medical Device Evaluation’s public consultation on the Guidelines on the Medical Device Product Technical Requirements Compilation Registration Review (2021 Revision) (Draft for Comments).
Read moreChina International Medical Device Regulatory Forum (CIMDR)
The Healthcare Equipment (HCE) Working Group and the Chamber's Cooperation Partner COCIR participated in the largest medical device regulatory event in the world, the 12th China International Medical Device Regulatory Forum (CIMDR).
Meeting on AI Medical Devices Development with National Medical Products Administration (NMPA)
Meeting on AI Medical Devices Development with National Medical Products Administration (NMPA)
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