Advocacy Actions
European Chamber Representatives Made Presentations during the Nickel Institute China Chemical Regulatory Workshop 2019
On 17th Sept., European Chamber representatives Michelle ZHANG, Government Relations Manager, and Rachel RAPAPORT, Working Group Coordinator, made presentations in the China Chemical Regulatory Workshop 2019, organized by the Nickel Institute. The theme of the workshop was Chemical Risk Assessment and Management.
Read moreComments to the SAMR's Interim Measures for Handling Complaints and Reporting in Market Supervision and Administration (Draft for Comments)
On 17th September, the Chamber submitted comments to the State Administration for Market Regulation on the Interim Measures for Handling Complaints and Reporting in Market Supervision and Administration (Draft for Comments).
Read moreComments to the Ministry of Industry and Information Technology (MIIT) on the Guiding Opinions on Industrial Big Data Development (Draft for Comments)
The European Chamber's ICT and Cybersecurity working groups submitted collated comments to the MIIT on the Guiding Opinions on Industrial Big Data Development (Draft for Comments). The comments mainly called for the clarification of certain concepts such as some platforms including the resource platforms for national basic industrial data, and some subjects including the big data solution provider, the technology provider for industrial internet platform and the integration solution provider for intelligent manufacturing system.
Read moreComments to the National Medical Products Administration on the Regulations on Random Inspection of Medical Devices Quality
On 27 August 2019, the Department of Comprehensive Affairs from National Medical Products Administration (NMPA) has initiated public consultations on Regulations on Random Inspection of Medical Devices Quality.
Read moreComments to the NMPA's Public Consultation on the Regulations on Random Inspection of Medical Devices Quality (Draft for Comments)
On 12th September, the medical device sector submitted comments to the National Medical Products Administration on the Regulations on Random Inspection of Medical Devices Quality (Draft for Comments).
Read moreGovernment Affairs Forum Event - Expert Insight Sharing - Status of the US-Chian relations and Trade Conflict
On 12th Sept., John Holden, senior director and head of China Practice at McLarty Associates, shared his insights on U.S-China relations to members of the European Chamber Government Affairs Forum.
Read moreMeeting with Tianjin Industry and Information Technology Bureau on Intelligent Manufacturing
On 11 September 2019, an European Chamber Tianjin Chapter delegation led by Dr. Juergen Hasenpusch, board member of Tianjin local board met with Mr. Zhao Peng, Department of Equipment Industry, Tianjin Municipal Industry and Information Technology Bureau (TJMIIT) on the theme of Tianjin intelligent manufacturing support policies.
Read moreEuropean Chamber meets DG GROW Representative
On Wednesday, 11th September, European Chamber Business Managers and Coordinators representing the Automotive, Shipbuilding, Inter-Chamber SME and Standards and Conformity Assessment Working Groups, met the newly appointed DG GROW representative in China, Mr. Frank Schmiedel.
Read moreComments to the CMDE's draft 'Guidelines for Clinical Trials of Hernia Patches'
The Healthcare Equipment (HCE) Working Group submitted comments to Centre of Medical Device Evaluation's (CMDE's) draft 'Guidelines for Clinical Trials of Hernia Patches'.
Meeting with Chongqing Economy and Informatization Commission
On 10th September, European Chamber Southwest Chapter General Manager Sally Huang, and Chongqing Office Manager Camellia Song met with Chongqing Economy and Informatization Commission led by Chi Fu, Director of Foreign Economy and Foreign Affairs Office.
Read more