Advocacy Actions
Meeting of the EU-China Medical Device Expert Roundtable (MDER) IV
The six working groups reported interim findings and recommendations to EU and China Authorities, at this the 4th phase of EU-China Medical Device Expert Roundtable (MDER IV)
Read moreDG GROW - AQSIQ Working Group Meeting on Medical Devices
DG GROW and AQSIQ had their working group meeting on medical devices. COCIR SG and COCIR China representative were invited to joined the meeting.
Read moreComments on RoHS II Compliance Management Catalogue was debriefed to EUD
Comments on RoHS II Compliance Management Catalogue was debriefed to EUD
Read moreSeminar on Remanufacturing of Medical Imaging Equipment
Successful Seminar on Remanufacturing of Medical Imaging Equipment
Read moreComments on RoHS II Compliance Management Catalogue
Comments on RoHS II Compliance Management Catalogue was submitted to MIIT
Read moreMeeting with CFDA on Spare Parts Issue
Meeting with CFDA Department of Medical Device Registration on spare parts of medical equipment, and their registration.
Read moreLobby Letter submitted to BJ Gov. on the challenge of oversea type testing
A lobby letter was submitted to BJ Gov. on the challenge of oversea type testing
Read moreFollow-up proposal submitted to CFDA on regulation of spare parts for medical equipment
A follow-up proposal was submitted to CFDA on regulation of spare parts for medical equipment
Read moreBrain storming with China Society for Drug Regulation on EU-China Medical Device Expert Roundtable
Brain storming with China Society for Drug Regulation (CSDR) on the cooperation concerning EU-China Cooperation Project - Medical Device Expert Roundtable (MDER)
Read moreOverview on EU Medical Device Regulation / IVD Regulation - COCIR-EUCCC contribution to CFDA
Overview on EU Medical Device Regulation / IVD Regulation - COCIR-EUCCC contribution to CFDA
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