Advocacy Actions
Training on the Direct on-line Reporting System for Voluntary Recalls of Medical Devices
Organized by the Healthcare Equipment Working Group of the European Chamber, and supported by the SHFDA, the launching training on the direct on-line reporting system for voluntary recalls of medical devices was successfully held in Shanghai.
Read moreComments on the NMPA's draft "Regulation for Supervision of Customised Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments on the National Medical Product Administration's (NMPA, the former CFDA) draft "Regulation for Supervision of Customised Medical Devices".
Read moreMeeting with Shanghai Municipal Government Development and Research Center on 2018 Shanghai International Think Tank Summit
Chamber representative met with the Shanghai Municipal Government Development and Research Center on the 2018 Shanghai International Think Tank Summit.
Comments to the CMDE's Draft "Guideline for the Evaluation of Spinal Implants Clinical Study Results"
The Healthcare Equipment (HCE) Working Group submitted comments to the Centre of Medical Devices' (CMDE) draft "Guideline for the Evaluation of Spinal Implants Clinical Study Results".
Read moreMeeting with State Council Research Office
On 23rd October, State Council Research Office hosted a meeting. European Chamber of Commerce in China and representatives of certain companies attended the meeting. State Council Research Office welcomed attendees and expected honest and open suggestions on how to improve FIE’s (foreign-invested enterprise) business environment in China.
Read moreChamber Representatives Speak at Seminar on Local Business Environment and Social Security Policy Changes
Chamber Representatives Speak at Seminar on Local Business Environment and Social Security Policy Changes
Read moreComments on the CMDE's draft "Guideline for Evaluation of Respiratory Virus Detection Reagents based on Multiplex Nucleic Acids"
The Healthcare Equipment (HCE) Working Group submitted comments to the Centre of Medical Device Evaluation's (CMDE) draft "Guideline for Evaluation of Respiratory Virus Detection Reagents based on Multiplex Nucleic Acids".
Read moreComments to the National Centre for Adverse Drug Reaction Monitoring on Draft Guidelines on Medical Device Adverse Events Reporting
The Healthcare Equipment (HCE) Working Group submitted comments to the Centre for Adverse Drug Reaction (ADR) Monitoring on five different Draft Guidelines on Medical Device Adverse Events.
Read moreMeeting with Ministry of Finance and China Council of the Promotion of International Trade
On October 19th, a delegation from the Chamber attended the meeting, which was co-hosted by MOF and CCPIT. A few representatives from USCBC, AmChem and American companies attended as well and made inputs accordingly. The general discussion was on how to improve the business environment in China.
Read moreMeeting with China Centre for Promotion of SME Development
On Friday, 19th October, Advocacy and Working Group Coordinator Ester Cañada Amela meet Mr. Miao Changxing, Director General of the China Centre for Promotion of SME Development and China International Cooperation Association of Small and Medium Enterprises.