Preparing for Regulatory and Technological Change across the Medical Device Landscape with InnoScot Health
Join us for the next in our series of informative webinars – Preparing for Regulatory and Technological Change across the Medical Device Landscape with InnoScot Health
InnoScot Health, which has a strong record of protecting the interests of NHS Scotland, believes it is crucial for innovators to get the right regulatory advice, support, and signposting, and that understanding the implementation and transition plan for new medical device legislation is a key asset.
The session, taking place Wednesday 24 May, 12pm - 12.45pm will be introduced and led by Head of Regulatory Affairs, Elaine Gemmell and Project Manager Paula Sweeten, who will be joined by Senior Clinical Advisor, Software and AI, of the Innovative Devices Division at the Medicines and Healthcare products Regulatory Agency (MHRA), Dr Paul Campbell.
Pre submit your questions for our panel discussion to [email protected].
Register to attend
The session will be a great opportunity to learn about the importance of ensuring the supply of safe, effective, and innovative medical products against a backdrop of substantial reform to the current regulatory framework, as well as to learn about what can be expected in medical device innovation in the near future, particularly the application of artificial intelligence (AI) in healthcare.
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