Advocacy Actions
Meeting with China Association of Medical Equipment
EUCCC HCE WG and COCIR will contribute to the Development Status and Trend of Medical Equipment in China, the "Green Book" for medical equipment in China.
Read moreShare industry comments with EUD for WTO Notification G/TBT/N/CHN/1313
Share industry comments with EUD for WTO Notification G/TBT/N/CHN/1313, Amendments to Regulations for the Supervision and Administration of Medical Devices (Draft)
Read moreSeminar of Center for Medical Devices Evaluation on Electronic Regulated Product Submission
On 18th March, the Center for Medical Devices Evaluation of National Medical Products Administration invited the Chamber for a seminar regarding the "Technical Guideline for "eRPS, Electronic Regulated Product Submissions".
Read moreLobby Letter on the Implementation of the Measures for the Administration of Medical Device Adverse Event Monitoring and Re-evaluation
COCIR, Consumable and Disposable Medical Devices Advisory Committee and Healthcare Equipment Working Group submitted a lobby letter to China Center for Food and Drug International Exchange and Center for Drug Re-evaluation of National Medical Products Administration, regarding the implementation of the Measures for the Administration of Medical Device Adverse Event Monitoring and Re-evaluation.
Read moreSeminar with Center for Drug(Device) Re-evaluation on Adverse Events Reporting
The Chamber Healthcare Equipment Working Group was invited to attend the Seminar organized by NMPA to discuss three key Guidelines developed by Center for Drug(Device) Re-evaluation. Members' concerns and recommendations were raised by EUCCC HCE representatives, during the meeting.
Read moreAttend CMDE Seminar on ICH Efficacy Guidelines
Attend Seminar of Center for Medical Device Evaluation on ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use) Efficacy Guidelines
Read moreGenerate a report to CMDSA on Ecodesign of Medical Equipment in EU from energy consumption perspective
Generate a report to Center for Medical Device Standardization Administration on Ecodesign of Medical Equipment in EU from energy consumption perspective.
Read moreComments to the SAMR's "Supervision of Agents for Imported Medical Devices" Public Consultation
On 24th December 2018, State Administration of Market Regulation (SAMR) published the second draft of Supervision of Agents for Imported Medical Devices.
Read moreupdate the Key Market Access Barrier List for China, for medical device sector
Feedback to Delegation of the European Union to China (EUD) regarding the European Commission on Key Market Access Barrier List for China, for medical device sector
Read moreEvent on "The Development of Medical Imaging Technology in the Past 40 years"
A seminar at the Belgium Embassy on the Development of Medical Imaging Technology in the Past 40 years: How Foreign Investment in Healthcare can Support Healthy China 2030
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