Advocacy Actions
Workshop with the German Ministry of Health and Shenzhen Customs on EU Medical Device and In Vitro Diagnostic Regulations
The Deutsche Gesellschaft für Internationale Zusammenarbeit (GIZ) and Shenzhen Customs Authorities jointly hold a workshop together with the German Ministry of Health (BMG) on EU Medical Device (MDR) and In Vitro Diagnostic Regulations (IVDR).
Read moreChina International Medical Device Regulatory Forum (CIMDR)
The Healthcare Equipment (HCE) Working Group and the Chamber's Cooperation Partner COCIR participated in one of the largest medical device regulatory event in the world, the 13th China International Medical Device Regulatory Forum (CIMDR).
Read moreRecommendations to NMPA’s draft Regulations on Administration of Medical Devices for Emergency Use
Recommendations to NMPA’s draft Regulations on Administration of Medical Devices for Emergency Use
Read moreMeeting with Hainan Free Trade Port Working Group
On 14th February, European Chamber had a meeting with Hainan Free Trade Port Working Group. During the meeting, European Chamber and Hainan Free Trade Port Working Group discussed the latest policy updates and potential cooperation areas.
Read moreMeeting with NMPA on Draft Implementation Document of GB9706 Series Standards
Meeting with NMPA on Draft Implementation Document of GB9706 Series Standards
Read moreRecommendations to the Southern Medicine Economic Research Institute on "2022 China Medical Device Industry Development Report"
Recommendations to the Southern Medicine Economic Research Institute on "2022 China Medical Device Industry Development Report"
Read moreComments to NMPA re. the Enterprise implementation of the main responsibility for quality and safety of medical devices supervision and management regulations
Healthcare Equipment Working Group collected comments to the National Medical Products Administration on the Enterprise implementation of the main responsibility for quality and safety of medical devices supervision and management regulations (Draft for Comments).
Read moreOnline Preparatory Meeting with the German Federal Ministry for Economic Affairs and Climate Action (BMWK) for Sino – German dialogues on accreditation, conformity assessment, product safety and market surveillance
The Healthcare Equipment (HCE) Working Group particapated in an online preparatory meeting with the German Federal Ministry for Economic Affairs and Climate Action (BMWK) for Sino – German dialogues on accreditation, conformity assessment, product safety and market surveillance, organised by the German Association for International Cooperation (GIZ).
Read moreRecommendations to NMPA re. Implementation of Mandatory Standards-GB9706 Series Standards
Recommendations to NMPA regarding Implementation of Mandatory Standards-GB9706 Series Standards
Read moreMeeting with CAICT Discussing on Domestically Manufactured Medical Equipment Supply Chain Issue
Meeting with the China Academy of Information and Communications Technology (CAICT) Discussing on Domestically Manufactured Medical Equipment Supply Chain Issue
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