Advocacy Actions
Conference with the Centre for International Economic and Technology Cooperation (CIETC) on Carbon Neutrality Policy and Path in China and Europe
The European Chamber co-organised the event “Carbon Neutrality Policy and Path in China and Europe” along with the Centre for International Economic and Technology Cooperation (CIETC) of the Ministry of Industry and Information Technology (MIIT) on Monday 26th April at 14:00-17:00 at European Chamber Beijing Office.
Read moreMeeting with the Centre for Medical Device Evaluation on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents
On 26 April, the medical device sector had a meeting with the Centre for Medical Device Evaluation on the Technical Guidance on the Usage of Overseas Clinical Trial Data of In Vitro Diagnostic Reagents.
Read moreLobby letter to NMPA about transition period in Administration of Cosmetics Labelling
The Cosmetics Desk submitted a lobby letter to NMPA about the transition period in Administration of Cosmetics Labelling.
Read moreVisit to Tianjin Development and Reform Commission
On 25 April, The Chamber Tianjin Chapter, Catherine Guo, General Manager of Tianjin Chapter paid a visit to Foreign Capital and Overseas Investment Department of Tianjin Development and Reform Commission and met with Director Ma Te. Each side introduced the responsibilities and services to foreign investment. Director Ma expressed strong willingness of further cooperation with the European Chamber Tianjin Chapter.
Read moreComments to NMPA on the Administrative Measures for Medical Device Registration (Revised Draft for Comments)
On 25 April, the medical device sector sent omments to the National Medical Products Administration on the Administrative Measures for Medical Device Registration (Revised Draft for Comments).
Read moreComments to NMPA on the Administrative Measures for In Vitro Diagnostic Reagents Registration (Revised Draft for Comments;)
On 25 April, the medical device sector sent comments to the National Medical Products Adminstration on the Administrative Measures for In Vitro Diagnostic Reagents Registration (Revised Draft for Comments).
Read moreComments to NMPA on the Administration Measures for Supervision of Medical Device Manufacturing (Revised Draft for Comments)
On 25 April, the medical device sector sent comments to the National Medical Products Administrtaion on the Administration Measures for Supervision of Medical Device Manufacturing (Revised Draft for Comments).
Read moreComments to NMPA on the Administrative Measures for Medical Device Trading Operations (Revised Draft for Comments)
On 25 April, the medical device sector sent comments to the National Medical Products Administration on the Administrative Measures for Medical Device Trading Operations (Revised Draft for Comments).
Read morePhonecall with SAMR on Local Gas Adaptability Test
The local gas adaptability test is a long last issue which raise ECHI member concerns. and that is also the KR 2.1.2 content for 2021 ECHI Paper.
Read moreComments to the Ministry Public Security on the Road Traffic Safety Law (2021 Revised Draft for Comments)
The European Chamber submitted collated comments to the MPS on the Road Traffic Safety Law (2021 Revised Draft for Comments).
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