Brian Cleary, MS
Mr. Cleary works with CardioMed Device Consultants as an affiliate consultant. Brian possesses 20 years of clinical, quality and regulatory experience within the medical device industry, spanning a broad range of orthopedic, cardiovascular, peripheral vascular, neurovascular, and neurostimulation product technologies. He has extensive success in regulatory strategy development and execution, including multiple US FDA 510(k) clearances and IDE and PMA approvals, as well as, CE Mark Technical File and Design Dossier approvals.
Prior to embarking on a successful consulting career, Brian held management positions within multiple medical device companies, including Medtronic Vascular (AVE), Ekos Corporation, Northstar Neuroscience and, most recently, Pathway Medical.
Mr. Cleary is a member of the Regulatory Affairs Professional Society (RAPS).