Dr. Roberto Liddi
Chief Regulatory, Quality & Information Governance Officer (CRQO)
Dr. Roberto Liddi is an experienced commercial leader with over 20 years' experience in medical device manufacturing. He is skilled in U.S. Food and Drug Administration (FDA) regulations, Regulatory Strategy, Corrective and Preventive Action (CAPA), Quality Auditing, and CE marking.
Roberto is a Doctor of Biological Sciences focused in Human Biology, and studied at Università degli Studi di Bari. He held director level positions with Cozart (now Abbott Diagnostics), Zimmer Biomet, KCI (now Acelity) and Renishaw, before being appointed VP Quality and Regulatory with Sensyne Health in June 2018.
He has been an active member of several European Commission working groups, advising on Medical Device Regulations, 3D printing for custom made devices, human tissue regulations and risk analysis. He is a member of TOPRA and a lecturer in Regulatory Affairs at School of Life & Medical Sciences, University of Hertfordshire (TOPRA).