Lobby Actions

2014-09-05 > Shanghai

Meeting with Shanghai Customs

Shanghai Customs Updates on China (Shanghai) Pilot Free Trade Zone

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2014-09-05 > Nanjing

Dinner with the Vice Mayor of Nanjing

On 4th September, the Mayor of Nanjing Mr Miao Ruilin invited the European Chamber Nanjing Chapter to celebrate the Mid-Autumn Festival at Nanjing Zijin (Jiangning) Technology Incubation U-Lake Centre.

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2014-09-03 > Beijing

Meeting with DG WTO Affairs, MOFCOM

On September 3rd, European Chamber representatives led by Vice President Sara Marchetta met with Madame Zhao Hong, Director General and Chief WTO Negotiator of MOFCOM’s WTO Affairs Department.

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2014-09-02 > All chapters

Working Group Meeting on the Revised Consumer Protection Law

The Agriculture, Food and Beverage Working Group invited Ms. Jiaoli Zhao, Deputy Director, Shanghai Consumer Council to give a talk on the Revised Consumer Protection Law.

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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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2014-09-02 > Beijing

Submit Comments to CFDA on Guidance for Clinical Evaluation

Submit Comments to CFDA on Guidance for Clinical Evaluation

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2014-09-01 > Beijing

EU-China Medical Device Expert Roundtable (MDER) III Plenary Meeting

MDER is with the purpose to study and compare the EU and China Medical Device regulatory requirements, and then give recommendations to both EU and China authorities, for a harmonized regulatory system. MDER III focus on below topics -
• WG 1 : Medical Device Registration submission requirements, and product changes’ registration
• WG 2 : Clinical evaluation
• WG 3 : In-Vitro Diagnostic (IVD)

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2014-08-31 > Beijing

Submit Comments to CFDA on Guidance for Clinical Trials of IVD Reagents> and <Guidance for Compiling Instructions for IVD Reagents

Submit Comments to CFDA on Guidance for Clinical Trials of IVD Reagents> and <Guidance for Compiling Instructions for IVD Reagents

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2014-08-30 > Beijing

Seminar on China's New Regulations of Medical Device

To prepare for this seminar, EUCCC, jointly with Amcham, as well as China Association for Medical Device Industry (CAMDI), had meetings with members and consolidated comments / suggestions, and submitted to CFDA, requesting for clarification/advice from CFDA during the seminar.

Mr. Zhang introduced overall revisions of medical device regulations from Legal perspective. SUN briefed about ideas for post-market surveillance supervision, manufacturing, distributing. DENG presented mainly for medical device registration regulations’ revision.

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2014-08-30 > Beijing

Submit Comments to CFDA on Naming Rules for Medical Equipment (Draft for Comment)

Submit Comments to CFDA on Naming Rules for Medical Equipment (Draft for Comment)

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