Advocacy Actions
EU-China Cosmetics Regulation Seminar
EUCCC Cosmetics Working Group organized a seminar on EU-China Cosmetics Regulation, focusing on EU Responsible Person System and post market surveillance system. Both side also discussed the Pudong pilot on imported non special notification, the plan of the government, and the concerns from the industry in the process of pilot implementation.
Meeting with Shanghai Pudong Market Supervision Bureau
CE and EUCCC are going to help to arrange the official visit of Pudong Market Supervision Bureau to France and Belgium in Oct. this year. We discussed the purpose of their visit and learned that with regard to the overall programme, they hoped to see a comprehensive programme, covering more aspects, including cosmetics regulation, R&D, innovation, further development trends, manufacturing/GMP, Distribution management, border line products classification and management, “special cosmetics” management (baby products, products for pregnant women), cooperation between member states of EU and the EU commission, etc. After the visit, Pudong market supervision bureau is going to submit a study report with regard to overall cosmetics regulation reform to Shanghai FDA and CFDA.
Read moreLetter to Medical Insurance Department of MOHRSS on Drug Renaming in NRDL
Letter to Medical Insurance Department of MOHRSS on Drug Renaming in NRDL
Read moreMeeting with China Food and Drug Administration
Cosmetics Europe and EUCCC Cosmetics Working Group visited Cosmetics Division, CFDA to discuss cosmetics products management, ingredients management, Pudong pilot on non-special cosmetics notification, and possible cooperation between China and EU on cosmetics regulation.
Read moreLobby Letter to CFDA on Implementing Date of Registration Requirements for Exported Infant Formula and Food for Special Medical Purpose
The Paediatric Nutrition Desk submitted a lobby letter to the CFDA on the implementing date of the grace period for the exported infant formula and food for special medical purpose to get registered.
Read moreThe 10th Year China Anti-monopoly Legislation Review & Anticipation Conference
The 10th Year China Anti-monopoly Legislation Review & Anticipation Conference was Held in Beijing
Read moreMeeting with CFDA Center for Medical Device Evaluation
Meeting with new head of CMDE and raised key concerns of the industry
Read moreComments on CFDA's Draft "Catalogue of IVD Products Exempt from Clinical Trials"
The Healthcare Equipment (HCE) Working Group submitted Comments on the CFDA's Draft "Catalogue of IVD Products Exempt from Clinical Trials"
Read moreDialogue with European Chemicals Agency (ECHA) on EU-China Chemical Cooperation
During this meeting, the Petrochemicals, Chemicals and Refining WG has had a dialogue with Mr Geert Dancet, Executive Director of the European Chemicals Agency (ECHA). Likewise, the working group will introduce its activities and publications, including the Position Paper 2017/2018 currently under preparation to Mr Dancet.
The working group has held a discussion on ECHA and EU’s chemicals legislations and ECHA’s enhanced dissemination of information on chemicals. Additionally, Mr Dancet has debriefed our members on ECHA visit to China.
Meeting with European Commission’s Joint Research Committee
The European Chamber met with a delegation of the European Commission’s Joint Research Centre in order to present the European Chamber’s Research and Development (R&D) Working Group and China’s R&D policies. The European Chamber also presented the key finding of the Business Confidence Survey 2017 related to innovation.
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