Michael Dunning

Michael Dunning is a seasoned professional in regulatory affairs and quality management, currently serving as a Senior Regulatory Affairs Consultant at Merit Medical Systems, Inc. since September 2021. In this role, Michael is a key member of the regulatory core team focusing on EU MDR Class III implantable device remediation and technical file preparation for submissions. Prior experience includes positions such as Senior Regulatory Affairs Specialist and Interim QA/RA Director at Surmodics, EMEA North Quality & Regulatory Compliance Manager at Zimmer Biomet, and Head of Quality Management at B. Braun Group. Michael's extensive background also encompasses roles at Zimmer Biomet, Integer Holding Corporation, Integra LifeSciences, and Boston Scientific, where responsibilities have ranged from quality assurance to regulatory submissions across multiple regions including the US, EU, and Canada.