Medical Device
Why is Medical Technology Getting Shrouded by the Fear of Cybersecurity Issues?
Labeling Requirements for Medical Devices
USA: FDA Modifies List of Standards for Premarket Device Reviews
USA: FDA Drafts Guidance on Patient Engagement in Device Trials
China: NMPA Joins IMDRF’s Post-Market Device Safety Data Exchange Scheme
Uncertainty as a Factor in Determining Benefit-Risk for Pre-market Approval of Medical Devices
The First Step
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