Introduction to the regulatory requirements for clinical investigation
With InnoScot Health’s Head of Regulatory Affairs, Elaine Gemmell
22/10/2025
2:00 pm
1hr
All medical devices to be used on humans must be UKCA/CE marked for the purpose they are being used, unless they are being used as part of a clinical investigation designed to investigate the performance and safety of the medical device or accessory.
In order to use a medical device in a clinical trial to produce clinical evidence for regulatory purposes, certain conditions need to be met.
This webinar will provide an introduction to conditions that need to be met to conduct these trials.
If you are interested in attending, please email TayHealthTech@hw.ac.uk for the link.
