Advocacy Actions
Meeting with the Centre for Medical Device Evaluation of the National Medical Product Administration on Guideline for the Evaluation of Clinical Studies for IVD Reagents
Following the public consultation in last December, the Centre for Medical Device Evaluation of the National Medical Product Administration held a meeting on Guideline for the Evaluation of Clinical Studies for IVD Reagents.
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.
Read moreEuropean Chamber Members Participate Medical Device Evaluation Reform Roundtable with NMPA
On 24th July, the Chinese Centre for Medical Device Evaluation of the National Medical Products Administration (the Centre) held a roundtable meeting as part of the ‘Remaining True to Original Aspiration and Keeping Mission Firmly in Mind’ initiative.
Read moreSupplementary Report on Medical Device Standards to the Centre for Medical Device Evaluation
On 23rd July, the medical device sector submitted the supplementary material on standards to the Centre for Medical Device Evaluation.
Read moreCAME: Seminar Medical Device Sourcing
In the framework of its Annual Conference, the China Association of Medical Equipment (CAME) hold a seminar on procurement of medical devices
Read moreComments to Guangdong HSA on "Administration of Prices for New Medical Services"
The Healthcare Equipment (HCE) Working Group submitted comments on "Administration of Prices for New Medical Services" to the public consultation by the Healthcare Security Administration (HSA) of Guangdong Province.
Read moreMeeting with the Shanghai Customs on Medical Device Customs Clearance Inspections Issues
On 17th July, the medical device sector visited the Shanghai Customs for medical device customs clearance inspections issues.
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