Advocacy Actions
meeting with China Society for Drug Regulation (CSDR)
Meeting with China Society for Drug Regulation - Jessica Yuan will join the Legislative Research Group on future Law of P.R.China on the Administration of Medical Devices
Read moreMeeting with the International Cooperation Department on Proposals for NMPA's Visit to Russia
Meeting with the International Cooperation Department on Proposals for NMPA's Visit to Russia, like to meet with the Association for Medical Devices
Read moreProvide a presentation on "Buy China" Issue in medical device sector to be discussed with DG TRADE
Public Procurement in China: preference to domestic brands! COCIR Office in Europe will communicate and ask for support from DG GROW and DG TRADE
Read moreAdvocacy Letter to the Enforcement and Anti-Monopoly Division of the Guangxi Administration for Market Regulation
On 20th August, the medical devices sector submitted an advocacy letter to the Enforcement and Anti-Monopoly Division of the Guangxi Administration for Market Regulation.
Read moreLobby Letter to Supervisory Office, General Office of State Council on "Domestic Brand" Procurement Issue
Public Procurement in China: Preference to Domestic Brands! Actions being taken by COCIR/HCE WG
Read moreAdvocacy Letter to the National Medical Products Administration on Government Information Disclosure
On 14th August, the Medical Device Sector submitted an advocacy letter to the National Medical Products Administration on government information disclosure.
Read moreSubmitted Comments to the National Medical Device Administratio and the Centre for Drugs (Medical Devices) Re-evaluation on the Periodic Risk Evaluation Report
On 31st July, the medical device sector submitted comments to the National Medical Device Administration and the Centre for Drugs (Medical Devices) Re-evaluation on the Periodic Risk Evaluation Report.
Read moreElectronic Regulated Product Submission Workshop
on 26th July, medical device sector organized a workshop on the recently launched electronic Regulated Product Submission.
Read moreSubmitted Recommendations on Medical Device Customs Clearance Inspection to Shanghai Customs
Following the visit to Shanghai Customs on 17th July, the medical device sector submitted recommendations on medical device customs clearance inspection to Shanghai Customs.
Read moreSubmitted DITTA's New Work Item Proposal on Post-Market Clinical Follow-Up Studies to the National Medical Products Administration
On 24th July, DITTA submitted Post-Market Clinical Follow-Up Studies as the new work item extension for Management Committee Consideration.
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