Advocacy Actions
contribute industry good practices and documents to CMDSA on measurement of energy consumption
Contribute industry good practices and documents to the Center for Medical Device Standardization Administration (CMDSA) on measurement of energy consumption
Read morerecommendations after IMDRF 13th Meeting to CNDA
Recommendations of DITTA were submitted to the Chair after IMDRF 13th Meeting in Shanghai
Read moreIMDRF Management Committee meeting-open session, DITTA gave report
The 13th Management Committee meeting of International Medical Device Regulators Forum took place 20-22 March in Shanghai, COCIR at international level - DITTA (Global Diagnostic Imaging, Healthcare IT & Radiation Therapy Trade Association), was invited to attend, and gave report.
Read moreDITTA workshop on Cybersecurity
DITTA workshop on Cybersecurity, in the framework of the International Medical Device Regulators Forum’s (IMDRF) 13th Management Committee (MC) meeting
Read moreParticipate and Present at CMDSA Seminar on energy efficiency evaluation
Present at the Center for Medical Device Standardization Administration (CMDSA) seminar on energy efficiency evaluation
Read moreFinish submission of FNGO Representative Office application dossier to the professional supervisory unit (PSU)
Finish submission of COCIR China Representative Office application dossier to the professional supervisory unit (PSU)
Read moreMeeting with CFDA on DITTA proposal for workshop during the 13th Meetings of IMDRF
Meeting with CFDA on DITTA proposal for workshop during the 13th Meetings of IMDRF
Read moreSubmit a letter to CFDA on Standardization Law article 27 and its application to medical devices
A joint letter by EUCCC and COCIR was submitted to CFDA requesting their advice with industry's recommendation on China Standardization Law article #27.
Read moreseminar on “EU Medical Device Regulation Changes and its Impact to Regulatory Environment in China” - Plenary
Plenary meeting - raise industry recommendations to CFDA with regards to Regulatory Environment in China for medical devices
Read moreSeminar on Medical Device Unique Device Identification (UDI) practice
COCIR and CDMD Desk members introduced UDI practice in Europe
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