Advocacy Actions
Attend CMDE Seminar on ICH Efficacy Guidelines
Attend Seminar of Center for Medical Device Evaluation on ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use) Efficacy Guidelines
Read moreComments to the WTO TBT on “Cosmetics Supervision and Administration Regulations”
WTO TBT called for public comments on “Cosmetics Supervision and Administration Regulations”. It was a good opportunity for the industry to raise our concerns again after the call for comments on this regulation by Ministry of Justice in last August. The WG also shared our comments to the EU delegation, Cosmetics Europe and PCPC.
Read morePresident Mats Harborn Visited Various European Officials in Brussels
President Mats Harborn Visited Brussels and Met with Cecilia Malmström, European Union Trade Commissioner, Michael Clauss, former German Ambassador to China, Zhang Ming, Chinese Ambassador to the EU, as well as Ann Mettler and Sylvia Hartleif of the European Political Strategy Centre.
Read moreComments to the CMDE's draft 'Master Document for Medical Device Registration'
The Healthcare Equipment (HCE) Working Group submitted comments to the Centre of Medical Device Evaluation's (CMDE) draft 'Master Document for Medical Device Registration'.
Read moreComments to the MoF's draft "Government Procurement Announcements and Information Release"
The Public Procurement Taskforce submitted comments to the Ministry of Finance's (MoF) draft "Government Procurement Announcements and Information Release".
Read moreComments to NPC on the Patent Law (Draft Amendment)
The European Chamber submitted collated comments on the draft amendment of the Patent Law to the Standing Committee of the National People's Congress.
Read moreComments to SAMR on the Provisions of Prohibiting Monopolistic Agreements (Draft for Comment)
The European Chamber submitted collated comments on the draft Provisions of Prohibiting Monopolistic Agreements to the State Administration for Market Regulation.
Generate a report to CMDSA on Ecodesign of Medical Equipment in EU from energy consumption perspective
Generate a report to Center for Medical Device Standardization Administration on Ecodesign of Medical Equipment in EU from energy consumption perspective.
Read moreComments to China National Institute of Standardization (CNIS) on the National Standard for Consumer Product Recall Electronics and Electrical Appliances Risk Assessment
Following the China National Institute of Standardization(CNIS)’s call for comments on the National Standard for Consumer Product Recall Electronics and Electrical Appliances Risk Assessment, and upon circulation of the draft within relevant working groups, the European Chamber has collated all member inputs and submitted to CNIS.
Read moreEuropean Chamber Meets with Executive Director of EASA
On 25th January, representatives of the European Chamber's Aviation & Aerospace Working Group met with the Executive Director of the European Union Aviation Safety Agency (EASA) to present the European Business in China — Position Paper 2018/2019 and discuss recent regulatory updates.
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