Explore the potential offered to MedTech sector businesses in different regulatory markets. Attend this session to discover current opportunities within the UK market and how to identify other world markets offering opportunities for your medical, digital and In Vitro diagnostic devices. As the EU continues to work through the EU MDR transition extension and the UK develops a new regulatory framework, it is critical to ensure that you keep up with changes and leverage the full potential of your devices to stay ahead of the competition.

Speaker: Matt Burton, Strategic Development Director, IMed Consultancy

Matt has over 12 years’ experience in QA/RA specialising in MDD/ UKCA and EU MDR. Representing many clients as UKRP, PRRC and with Global registrations, he’s worked with many devices over his Regulatory career from class I to class III and maintains many lasting client relationships. When he’s not at work, he’s usually surfing on the Devon coastline!

Location: UK Presentation Theatre: Hall 16, J48