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Matt Royle, PhD

Principal Regulatory Consultant
NAMSA

Matt supports medical device manufacturers worldwide to understand and meeting regulatory requirements in the EU. He has 20 years' experience in medical device research, product development and regulatory affairs. He has experience with start-ups, medium-sized, and multi-nationals, bringing new products to market and supporting existing portfolios, by providing leading roles in implementation of EU regulatory requirements. He has worked as a Notified Body Product Specialist for a number of years, specialising in conformity assessment of implantable class III and IIb orthopaedic joint replacement and sports medicine, spinal and bone grafting devices, as well as surgical instruments. Matt has a Master's degree in Mechanical with Medical Engineering from University of Leeds, a PhD in Medical Engineering from Queen Mary, University of London, and is a Chartered Engineering with the Institution of Mechanical Engineers.

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