Advocacy Actions

2020-03-12 > All chapters

Comments to the Chinese Mission to the EU on Wildlife Protection Law revision

Comments to the Chinese Mission to the EU on Wildlife Protection Law revision

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2020-03-06 > Beijing

Letter to the Department of Resource Conservation and Environment Protection, National Development and Research Commission (RCEP NDRC) on Cosmetics Contain Plastic Microbeads

The Cosmetics Working Group in the European Chamber submitted a letter to the Department of Resource Conservation and Environment Protection, National Development and Research Commission (RCEP NDRC), responding questions in terms of plastic microbeads that RCEP raised on the previous face-to-face communication on 16 January 2020.

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2020-02-20 > Beijing

Letter to Integrative Supervision Bureau of National Health Commission (NHC) on Urgent Import of Antibacterial Products and Simplified the Notification Process during the Epidemic of COVID-19

The European Union Chamber of Commerce in China submitted a letter to Integrative Supervision Bureau of National Health Commission (NHC), collating information in terms of urgent import of antibacterial products and simplified the notification process during the epidemic of COVID-19 following the practice of urgent import of medical devices.

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2014-12-05 > Beijing

Meeting with Bureau of Import and Export Food Safety, General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ)

On 5th December, EUCCC Cosmetic Working Group and AFB Working Group paid a visit to Bureau of Import and Export Food Safety, General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ).

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2014-12-01 > Beijing

Meeting with CAFFCI

On 1 December, CAFFCI organized a meeting for the industry representatives with Qi Liubin, Director of Cosmetic Division, Department of Drug and Cosmetic Registration.

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2014-11-24 > Beijing

Department of Legal Affairs Call for Comments on Draft of Cosmetic Supervision and Administration Regulation (CSAR)

EUCCC Cosmetic Working Group met the deadline set by Department of Legal Affairs on call for comments on draft of Cosmetic Supervision and Administration Regulation (CSAR) on 24 November.

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2014-11-21 > Beijing

Meeting with Department of Legal Affairs, CFDA on CSAR draft for comments

On 21 November, Department of Legal Affairs of CFDA called for a consultation meeting with participation of associations, chambers and representatives from leading domestic and foreign cosmetic companies, on the draft of Cosmetic Supervision and Administration Regulation (CSAR).

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2014-10-14 > Beijing

Presentation on CHMR by CAG professor at Cosmetics WG Meeting

Prof. Yang is one of the key consultants invited by CFDA Department of Legal Affairs on CHRM revision draft.

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2014-09-02 > Beijing

DG SANCO Meeting with China Food and Drug Administration

DG SANCO, CFDA, Chinese experts and EU experts in the cosmetics industry had a whole day communication and exchange on the regulatory and technical issues on 2 September. It was a very open discussion, and very well participated. All parties welcomed such a good communication opportunity, and agreed that it was a very healthy way to cooperate for both regulators and experts in China and EU side. In the morning session, EU experts introduced Animal Testing Bans in the EU and Status of Alternative methods, detailed introduction of the Safety Assessment Procedure of Finished Products and Efficacy Assessment Guideline on Cosmetics. In the afternoon session, CAFCCI expert and Shi Yue from IMPLAD introduced the 8783 version used ingredients list and responded to our reported suspicious missing ingredients by EUCCC Cosmetics Working Group. EU experts introduced the principles and Practical Aspects of Labelling of Cosmetics in the EU. Director Qi Liubin introduced the process of new ingredients registration, domestic non functional on line notification and imported non functional decentralization.

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2014-08-13 > Beijing

Lobby Letter to China CFDA – Missing Ingredients

On 13rd August 2014, the Cosmetic Working Group submitted a report to the China Food and Drug Administration regarding the suspicious missing ingredients based on the published 8783 version used ingredients list.

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