Advocacy Actions
Lobby Action on Car Repair Certification Study requested by MOT
Ministry inquiry regarding Car Repair and Maintainance system in Germany and U.S. as well as U.K.
Read moreComments to CAC on Critical Information Infrastructure Protection Regulations
The European Chamber submitted collated comments on the Critical Information Infrastructure (CII) Protection Regulations to the Cyberspace Administration of China (CAC).
Read moreComments to the CMDE on "Guideline on Technical Evaluation of Registrations of Hepatitis C Virus Nucleic Acid Genotyping Reagents"
The Healthcare Equipment Working Group submitted comments to the CMDE's draft "Guideline on Technical Evaluation of Registrations of Hepatitis C Virus Nucleic Acid Genotyping Reagents"
Read moreMeeting with CFDA on reprocessing of single-use devices
Meeting with the Department of Medical Device Registration of the CFDA on reprocessing of single-use devices
Read moreMeeting with CCPIT Nanjing
Mr. Bernhard Weber, Chair of European Chamber Nanjing Board met with Ms. Liang Jie, President of China Council for the Promotion of International Trade (CCPIT) Nanjing Sub-Council on 3 August 2017.
Read moreMeeting with Department of Economic Law of the NPCLAC
The Chamber had a meeting with Mr Yang Heqing, Deputy Director General of Department of Economic Law of the Legislative Affairs Commission of the National People’s Congress, NPCLAC.
Read moreComments to AQSIQ's Administrative Measures on General Certification of Imported Food (Draft for Comments)
Comments to AQSIQ on Administrative Measures on General Certification of Imported Food (Draft for Commnets)
Read moreComments to MIIT on <Compliance Management Catalogue of the Restriction of the Use of Hazardous Substances in Electrical and Electronic Products (First Batch)>
On 30th June, the Ministry of Industry and Information Technology (MIIT) issued a call-for-comments on the Compliance Management Catalogue of the Restriction of the Use of Hazardous Substances in Electrical and Electronic Products (First Batch) and Exempted list of the use of restricted substances of Compliance Management Catalogue. The European Chamber submitted the consolidated comments to the MIIT.
Read moreMeeting with Vice Administrator of SAC
The Chamber sent a delegation of seven members to attend a meeting with Vice Administrator Yu Xinli of the Standardization Administration of China.
Read moreComments on CFDA's Draft "Administration of Developing Standards for Medical Devices"
The Healthcare Equipment (HCE) Working Group submitted comments on the CFDA's Draft "Administration of Developing Standards for Medical Devices"
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