Innovation & Regulation: A medical device dialogue
Join the Centre of Excellence for Trials Collaboration for a full-day exploration of the medical device regulatory landscape, bringing together independent regulatory consultants and innovators from the University of Glasgow and the NHS
Through unique consultant-innovator paired presentations, this event offers real-world insights into navigating MedTech regulation. Sessions feature a regulatory expert discussing critical compliance aspects using University of Glasgow projects as case studies, followed by the innovator's firsthand perspective on their regulatory journey.
Lauren Brophy, Quality Manager at InnoScot Health, will present an ‘Overview of the Quality Management System’ from 3.15pm, with Russell Overend, Chief Operating Officer of MR CoilTech, presenting an ‘MR Coiltech case study' (Maintaining the QMS certification) as part of the same 30 min slot.
Register to attend
This is an invaluable networking opportunity for regulatory consultants, University of Glasgow and NHS healthcare innovators, research sponsors representatives, innovation support staff, and anyone working at the intersection of clinical practice, academic research, and MedTech development.
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