Marie Gallagher, Regulatory Affairs/Quality Consultant, Med-Di-Dia
Regulatory/Quality Consultant at Med-Di-Dia Limited - a consultancy firm based in Galway supporting Medical Device, In-Vitro Diagnostics and Digital Health companies offering a range of services. An experienced quality engineer with a proven track record of being a successful team leader and member, leading projects, and individual tasks to meet customer and business requirements while ensuring patient safety. She has worked closely with a number of regulatory agencies and notified bodies communicating effectively on behalf of Medical Device Companies. Her expertise includes Medical Device Regulation (MDR) remediation activities ensuring compliance with the applicable regulatory requirements.