Advocacy Actions
Submit COCIR contribution to CFDA on DRAFT Provisions on Medical Device After-sales Services
Submit industry comments to CFDA on DRAFT Provisions on Medical Device After-sales Services
Read moreSubmit a lobby letter to Jiangxi HFPC on a notice regarding reporting the information of medical equipment procurement
Submit a lobby letter to Jiangxi HFPC on a notice regarding reporting the information of medical equipment procurement.
Read moreMIIT seminar on RoHS, COCIR is one of the supporting organizations and gave presentation
RoHS seminar organized by MIIT, COCIR is one of the supporting organizations and presented on exemption procedure.
Read moreMeet with the Basel Convention Coordinating Centre for Asia and the Pacific
COCIR China Environmental Focus Group experts visit Basel Convention Coordinating Centre, explaining DITTA position on technical guidance of the Basel Convention
Read moreMeeting with CFDA on EU-China cooperation project - Medical Device Expert Roundtable (MDER)
Meeting with CFDA Medical Device Registration Department for MDER
Read moreSeminar with China Electronics Standardization Institute on China RoHS II
China's new regulations on Reduction of Harmful Substances (China RoHS II) will come into force on 01.Juli 2016. COCIR hold a seminar with the China Electronics Standardization Institute (CESI) to discuss details of the new regulations.
Read moreMeeting with European Commission DG GROW Deputy Director General Antti Peltomaki on EU-China Regulatory Dialogue
Representatives of the European Chamber met with a DG GROW delegation led by Deputy Director General Antti Peltomaki during this year's EU-China Regulatory Dialogue.
Read moreEuropean Chamber Comments on Administrative Measures on Energy Efficiency Labelling
中国欧盟商会关于《能源效率标识管理办法（修订征求意见稿）》的意见
Read moreJoint Working Group Meeting with Deputy Director General of Industrial Standards Department I of SAC
On 24 July 2015, members from the Standards and Conformity Assessment, Quality and Safety Services Working Groups as well as the COCIR Desk attended a joint meeting on social group standards.
Read moreMeeting with CFDA Medical Device Supervision Department and Privincial FDA on Administration Rules for the Issue of Export Certificates for Medical Devices
As the only foreign Chamber of Commerce, EUCCC was invited by CFDA Medical Device Supervision Dept. (MDSD) for a seminar with CFDA MDSD, provincial FDA, China Association for Medical Device Industry (CAMDI), some domestic companies and 2 foreign companies, discussing about the draft Administration Rules for the Issue of Export Certificates for Medical Devices.
Read more