Dan Clarke

Dan Clarke is a regulatory affairs professional with over 19 years of experience in the medical devices industry. They have held positions such as Senior Manager RA and QA at SFL Regulatory Affairs & Scientific Communication GmbH, focusing on consultancy for medical devices and in-vitro diagnostics. Previously, Dan worked at Baxter Healthcare Limited as a Research Scientist and Quality Engineer, gaining expertise in regulatory submissions and quality assurance processes. They completed a BSc in Chemistry from Loughborough University and hold a Regulatory Affairs Certificate in Medical Devices from RAPS. Currently, Dan serves as a Regulatory Partner at Roche.