Advocacy Actions
Comments to the CDR’s “Guideline for the Risk Assessment by the Medical Device Market Authorisation Holder (MAH)”
On 27 November 2018, the Centre for Drug Re-evaluation has initiated a public consultation on “Guideline for the Risk Assessment by the Medical Device Market Authorisation Holder (MAH)”.
Read morePresent Remanufacturing of Medical Equipment at China Remanufacturing Annual Conference 2018
COCIR presented at the China Remanufacturing Annual Conference 2018 on Circular Economy / Material Efficiency in EU
Read morea Briefing to COCIR Office in Brussels for their meeting with DG Trade
A briefing document on medical device industry procurement issues in China was developed for the meeting(s) in Brussels between DG Trade and COCIR Headquarter.
Read moreLobby Letter to Health Commision in Guangdong Province and Shenzhen City
HCE Working Group and COCIR submitted a lobby letter to Health Commission in Guangdong Province and Shenzhen city, regarding type B large medical equipment procurement.
Read moreInternational Medical Device Regulatory Forum (IMDRF) Stakeholder Forum
The 14. International Medical Device Regulatory Forum (IMDRF) stakeholder forum was organised by the Chinese National Medical Products Administration (NMPA). Representatives of the regulatory bodies of the world main economies, working groups of the IMDRF, the World Health Organization (WHO) and industry associations (including the Chamber's partner organisation Global Diagnostic Imaging, Healthcare ICT, and Radiation Therapy Trade Association (DITTA) presented their work.
Read moreCOCIR and HCE Members Contribute the 9th China International Medical Device Regulatory(CIMDR) Forum in Fuzhou
As the co-supporter of the 9th China International Medical Device Regulatory (CIMDR) Forum in Fuzhou, COCIR and several members of the Healthcare Equipment Working Groups attended the conference as the moderator and speaker for plenary and sub-forums.
Read moreSeminar on Environment Issues in Medical Equipment Sector
Seminar on Environment Issues in Medical Equipment Sector
Read moreComments to the CFDI's draft 'Inspection Points and Determination Principles for Medical Device Clinical Trials'
The Healthcare Equipment (HCE) Working Group submitted comments to the Center for Food and Drug Inspection of CFDA’s (CFDI) draft ‘Inspection Points and Determination Principles for Medical Device Clinical Trials’.
Read moreComments to the CNDA’s draft ‘Amendment for Reviewing Requirements of Renewal Registration and other Application Materials of Medical Devices’
The Healthcare Equipment (HCE) Working Group submitted comments to the China National Drug Administration’s (CNDA) draft ‘Amendment for Reviewing Requirements of Renewal Registration and other Application Materials of Medical Devices’.
Read moreMeeting with the Center for Medical Device Standardization Administration on Seminar with regards to environment issues in medical equipment sector
Meeting with the Center for Medical Device Standardization Administration on Seminar with regards to environment issues in medical equipment sector
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