Advocacy Actions
Comments to the State Administrative of Market Regulation (SAMR) on the Regulations on Proper Exercise of Discretion in the Imposition of Administrative Penalties
The European Chamber's Legal & Competition, and Fashion & Leather working group submitted collated comments to the SAMR on the Regulations on Proper Exercise of Discretion in the Imposition of Administrative Penalties by Administrative Departments for Market Regulation.
Read moreAdvocacy Letter to the National Medical Products Administration on the Registration and Administration of Blood Screening IVD Products
On 18th September, the medical devices sector submitted an advocacy letter to the National Medical Products Administration on the registration and administration of blood screening In Vitro Diagnosis products.
Read moreDITTA Chair Met with the Deputy Commissioner of NMPA
On 18th September, DITTA Chair met with the Deputy Commissioner of National Medical Products Administration.
Read morePlenary Session of the French Healthcare Alliance
On the annual plenary session of the French Healthcare Alliance the European Chamber presented on the latest developments in the Chinese healthcare reform and the opportunities and challenges for the French medical device industry.
Read moreEuropean 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.
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