Advocacy Actions
Comments to the European Commission on the Investment Restrictions on the Medical Device Sector in China
On 21st May, the medical sector submitted comments to the European Chamber regarding the investment restrictions on the medical device sector in China.
Read moreEUCCC Innovation Centre–Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-Off
On 17th May 2019, the European Chamber and the Centre for Medical Devices Evaluation (CMDE) of the National Medical Products Administration (NMPA), co-organized the Dialogue on the Evaluation for Innovative Medical Devices and eRPS Kick-off.
Read moreContribute to the "Green Book" of Medical Devices in China
Contribute to the "Green Book" of Medical Devices in China
Read moreSubmitted Comments to the Centre for Medical Device Evaluation on the draft Criteria for Establishing a Registration Project.
On 12th April 2019, the Centre for Medical Device Evaluation (CMDE) has initiated public consultations on the draft Criteria for Establishing a Registration Project.
Read morePreparatory Meeting for the 10th China International Medical Device Regulatory Forum
On the 24th April, the China Center for Food and Drug International Exchange and the Center for Medical Device Evaluation of the National Medical Products Administration held a preparatory meeting for the 10th China International Medical Device Regulatory Forum.
Read moreImplement smoothly the 1st review meeting with NMPA for a product, which secure the consequence that the European Chamber platform for reviewing innovative medical devices
Implement smoothly the 1st review meeting with NMPA for a product, which secure the consequence that the European Chamber platform for reviewing innovative medical devices.
Read moreMeeting with National Medical Products Administration on the Administration of Medical Device Adverse Event Monitoring
On 18th April, the National Medical Products Administration (NMPA), along with National and Provincial Centers for Adverse Drug Reaction (ADR) Monitoring, held a meeting regarding the administration of Measures on Medical Device Adverse Event Monitoring, and the Guideline for Monitoring Adverse Events in particular.
Read moreRoundtable Discussion with Sichuan Government on Business Environment in Sichuan
On 16th April, European Chamber delegates met with officials of Sichuan provincial government to discuss the business environment in Sichuan.
Read moreMeeting 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)
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