Advocacy Actions
Workshop with the Centre for Medical Device Evaluation on Guideline for Clinical Data Submission for Invitro-Diagnostic Products
Workshop with the Centre for Medical Device Evaluation on Guideline for Clinical Data Submission for Invitro-Diagnostic Products
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 moreMeeting on Development of Medical Device Industry with Peking University
Meeting on Development of Medical Device Industry with Peking University
Read moreMeeting with the Health Commission and the Healthcare Security Administration of Shandong Province on the Implementation of the Healthcare Reform
The Healthcare Equipment (HCE) Working Group hold a meeting with the Health Commission (HC) and the Healthcare Security Administration (HSA) of Shandong Province on the implementation of the Chinese healthcare reform in the province.
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 moreVideo Conference with the German Ministry of Economy and Energy (BMWi) and the Gesellschaft für Internationale Zusammenarbeit (GIZ) on Sino-German Quality Infrastructure Dialogue
Business Managers of the Healthcare Equipment (HCE) Working Group participated in a Video Conference with the German Ministry of Economy and Energy (BMWi) and the Gesellschaft für Internationale Zusammenarbeit (GIZ) on progress of the Sino-German Quality Infrastructure Dialogue.
Read moreLobby letter on the Administrative Measures on Mandatory National Standards
On 24th September various Working Groups sent a lobby letter on the implementation of the Administrative Measures for Mandatory National Standards.
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).
Pharmaceutical Working Group and Healthcare Equipment Working Group Meeting with EU Delegation and EU Member States Trade Consuls
On 17th September, European Chamber Pharmaceutical Working Group and Healthcare Equipment Working Group representatives met with EU Delegation and trade consuls from the General Consulates of Luxemberg, Austria, Belgium, Greece, Poland, Portugal, Sweden, Finland, Italy, the Netherlands, and Germany, and presented the work and key issues of the two working groups (WGs).
Read moreOnline Workshop with the Centre of Medical Device Evaluation (CMDE) on the Guideline for Evaluation of Medical Device Software
The Healthcare Equipment (HCE) Working Group and COCIR participated in full-day online workshop organised by the Centre of Medical Device Evaluation (CMDE) on the draft Guideline for Evaluation of Medical Device Software.
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