Advocacy Actions
Meeting with HFPC of Jiangxi Province on Procurement of Medical Devices
On 12. May 2016 the Health and Family Planning Commission of Jiangxi Province hat promulgated an "Implementation Plan for Sourcing of High-Value Disposable Medical Devices". A delegation of the CDMD Advisory Committee of the European Chamber met Mr. Tan Youwen, director of the Department of Financial Administration to discuss details of the Implementation Plan.
Meeting with the Procurement Centre for Medical Devices of Jiangxi Province on the Implementation of Purchasing Rules
In May 2016 the Health and Family Planning Commission of Jiangxi Province hat promulgated an "Implementation Plan for Sourcing of High-Value Disposable Medical Devices".
A delegation of the CDMD Advisory Committee of the European Chamber met Mr. Xi Zhong, director of the Procurement Centre of Medical Devices, to discuss question on the practical implementation of the .
Submit Comments to CFDA on On-Site Inspections of Clinical Trials for Medical Devices
The CFDA has published three regulations regarding On-Site Inspections of Clinical Trials for Medical Devices for public consultation, thereof two for the second round of consultation.
The European Chamber submitted consolidated comments on behalf of their members.
Comments on CFDA's Draft “Regulatory Guideline on Cold Chain (Transport, Storage) of Medical Devices”
On 06 May, the CFDA has initiated a Public Consultation on the Draft “Regulatory Guideline on Cold Chain (Transport, Storage) of Medical Devices”. In reply, the European Chamber has submitted consolidated comments on this draft regulation.
Read moreDiscussing with the EU Delegation for the outcomes of the ETWG meeting
A telephone with the EU Delegation for the outcomes of the ETWG meeting
Read moreLobby Letter to Drug Registration Department of the CFDA on Registration of Chemoluminescent Blood Screening Products
The Healthcare Equipment Working Group of the European Chamber Sent a Lobby Letter to the Department of Drug Registration of the CFDA to ask for acceptance of submissions for registration of chemoluminescent blood screening product.
Read moreMeeting with Drug Re-evaluation Center of CFDA
Met with Drug Re-evaluation Center of CFDA following up the status of the draft regulation on Medical Device Adverse Events Reporting
Read moreChina International Medical Device Regulatory (CIMDR) Forum 2016 – Preparation Meeting
JY as well as a few members were invited by CCFDIE for the preparation meeting of CIMDR 2016 on 13 April 2016.
Read moreMeet with CMDE Proposing Seminar with the Reviewers
JY as well as an expert from CDMD Advisory Committee met with Ms. An proposing and exploring possibility to have seminar(s) with Division III (for IVD products) of CMDE.
Read moreMeeting with Director of Dept. of Drug Policy of the Health and Family Planning Commission of Zhejiang Province
A delegation of the Healthcare Equipment Working Group of the European Chamber met with Mr. Wang Zhen, Director of the Department of Drug Policy and other officers of to discuss the purchasing regulations for consumable medical devices in Zhejiang Province.
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