Advocacy Actions
Meeting with DG Advertising Regulation, SAIC
On August 26th, European Chamber representatives met with Director General Zhang Guohua of SAIC’s Department of Advertising Supervision, to understand the status of the Advertising Law revision and discuss compliance issues faced by business in the Cosmetics and Paediatric Nutrition industry.
Read moreSubmit a Paper to CFDA on Questions and Suggestions in terms of the Implementation of Provisions on Medical Devices
Submit a Paper to CFDA on Questions and Suggestions in terms of the Implementation of Provisions on Medical Devices
Read moreSubmit Appreciation Letter to CFDA after the Key Provisions on Medical Devices were published
Submit Appreciation Letter to CFDA after the Key Provisions on Medical Devices were published
Read moreMeeting with DE CONNECT
On 18th August, the ICT Chairs briefed DG Kostas GLINOS for R&D, EU Commission on ICT indsutry's concerns and market access barriers to the China market. The conversation covers main obstacles such as access to China R&D Fund, Standard issues, information security, IPR and limited ICT market opening for foreign businesses. DG Kostas expressed the willingness of continue support for ICT WG and also proposed to create pilot EU-CN ICT projects for market entry, which is not limited to the Horizon 2020 but also other fund resources from EU Commission. In addition, DG Kostas confirmed that ICT WG members will be invited to join the next EU-CN IT Dialogues with MIIT in the future.
Read moreChina International Medical Equipment Exhibition & Scientific Conference CHINA-HOSPEQ 2014 Seminar on Medical Devices Registration Review
Supported by National Health and Family Planning Commission (NHFPC) and co-sponsored by IHECC of NHFPC, Chinese Hospital Association (CHA) and China Association of Medical Equipment (CAME), CHINA-HOSPEQ 2014 was held from August 15th to 17th, 2014. IHECC organized a close-door seminar on Medical Device Registration Review during the conference.
Read moreCCFDIE Task Force on Foreign Medical Device Regulatory System EUCCC-COCIR was invited to join the group
CFDA authorized the China Center for Food and Drug International Exchange (CCFDIE) to carry out a research on foreign medical device regulatory system comparison. The focus would be on supervision to medical device manufacturers and distributors, as well as post-market surveillance.
EUCCC-COCIR was invited to join the Task Force. And we are going to contribute from the aspects of post-market surveillance and manufacturing supervision.
Meeting with the National Health and Family Planning Commission
Representatives from the PN Desk discussed with the Director of the Division of Child Health Department to follow up with theircomments on the industry Code of Conduct.
Read moreSubmission of Comments to the China Food and Drug Administration
The Division Director of the Department of Law of the CFDA invited the PN Desk to submit comments on the draft Management Measures on Food Inspection and Sampling. The PN Desk submitted comments to the CFDA and will follow up with the CFDA for further actions.
Read moreLobby 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.
Read moreSubmission of A Lobby Letter to the China Food and Drug Administration
The PN Desk submitted a lobby letter on labelling requirement to the CFDA.
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