Advocacy Actions
Closed-door online briefing session on the European Commission’s initiative on an anti-coercion mechanism
On 3rd June the European Chamber invited Mr Colin Brown, Head of Unit, Legal Affairs/Dispute settlement at the European Commission, to brief key members on the Commission's initiative on an instrument to deter and prevent coercive actions by non-EU countries.
Read moreSubmitted comments on PBOC's Uniform Registration Measures for Moving Property and Rights Guarantees (Revised Draft for Comments)
The draft Measures are implementation measures of the People's Republic of China's Civil Code. Among other things, the NBFI WG suggested that registration of vehicles should be included in these Measures.
Read moreMeeting with Radio Regulation Bureau under the Ministry of Industry and Information Technology (MIIT) on the Radio Regulation of Automotive Radar
Meeting with Radio Regulation Bureau under the Ministry of Industry and Information Technology (MIIT) on the released draft for public consultation on Interim Provisions on Radio Regulation of Automotive Radar.
Read moreEU-China Intellectual Property Working Group Industry Session Meeting
The EU-China Intellectual Property Working Group Industry Session meeting was held on 2 June.
Read moreConclusion Meeting on the Recycling and Remanufacturing of High-end Medical Imaging Equipment
Conclusion Meeting on the Recycling and Remanufacturing of High-end Medical Imaging Equipment
Read moreComments to NMPA's Public Consultation on the Classification Rules for In Vitro Diagnostics
The medical devices sector sent comments to the National Medical Products Administration's public consultation on the Classification Rules for In Vitro Diagnostics.
Read moreComments to NMPA's Public Consultation on the In-Vitro Diagnostic Reagent Registration Application Data Requirements and Approval Document Format
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the In-Vitro Diagnostic Reagent Registration Application Data Requirements and Approval Document Format.
Read moreComments to NMPA's Pulic Consultation on the Medical Device Registration Application Data Requirements and Approval Document Format
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Medical Device Registration Application Data Requirements and Approval Document Format.
Read moreComments to NMPA's Public Consultation on the Category of Medical Devices Exempeted from Clinical Evalutaion
The medical devices sector sent comments to the National Medical Products Administration's (NMPA) public consultation on the Category of Medical Devices Exempeted from Clinical Evalutaion.
Read moreComments to NMPA's Public Consultation on the Technical Guideline for Methodological Comparison Of In Vitro Diagnostic Reagents Free of Clinical Trials
The medical devices sent comments to the National Medical Products Administration's (NMPA) public consultation Technical Guideline for Methodological Comparison Of In Vitro Diagnostic Reagents Free of Clinical Trials.
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