Seán is a graduate of University College Dublin where he completed his B.Sc. and M.Sc. studies, he also completed the M.Sc. in Medical Technology Regulatory Affairs at Cranfield University, UK. He has worked for over 15 years in the regulated medical device diagnostics industry in quality and regulatory affairs with extensive experience in CE marking and FDA submissions. He has senior management experience with SMEs and multinationals including due diligence and acquisitions activities, with in depth knowledge of design and development processes from concept to market authorizations for global regions.