Advocacy Actions
Meeting 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 moreMeeting with Vice Governor of Sichuan
On 17th April, the vice governor of Sichuan Provincial Government, Mr Wang Yihong, received a delegation from the European Chamber led by Vice President (VP) Massimo Bagnasco. Local Chair Paul Sives also joined the meeting.
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 moreComments to the National Health Commission on on the draft Measures for Clinical Use of Medical Devices
On 15th March 2019, National Health Commission (NHC) has initiated public consultations on the draft Measures for Clinical Use of Medical Devices.
Read moreInterviewed by China Pharmaceutical News on China led IMDRF WG's achievement
Interviewed by China Pharmaceutical News on China led IMDRF WG's achievement
Read moreSubmitted Comments to the Centre for Medical Device Evaluation on on the draft Evaluation of Deep Learning Assisted Decision-Making Medical Device Software.
On 1st February 2019, the Centre of Medical Device Evaluation (CMDE) has initiated public consultations on the draft Evaluation of Deep Learning Assisted Decision-Making Medical Device Software.
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)
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 more