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Dr Roberto Liddi
VP Regulatory & Compliance @ NuraLogix
Dr. Roberto Liddi is an experienced regulatory professional currently serving as the Vice President of Regulatory & Compliance at NuraLogix Corporation.12 He brings a wealth of expertise to this role, having worked extensively in the medical device manufacturing industry.
Professional Background
Dr. Liddi's skill set encompasses various aspects of regulatory affairs and compliance, including:
- U.S. Food and Drug Administration (FDA) Regulations
- Regulatory Strategy
- Corrective and Preventive Action (CAPA)
- Quality Auditing
- Risk Management
- CE marking
His experience spans multiple medical device sectors, including orthopedic devices, neurosurgical devices, 3D printed implantable devices, in vitro diagnostics (IVD), and Software as Medical Device (SaMD).1
Education and Expertise
Dr. Liddi holds a Doctorate in Biological Sciences, with a focus on Human Biology and Immunology from the Università degli Studi di Bari.12 This strong academic background complements his practical experience in the healthcare industry.
Career Highlights
Before joining NuraLogix, Dr. Liddi served as a member of the Advisory Group to the European Commission, demonstrating his influence in shaping regulatory policies at a high level.1 He joined NuraLogix Corporation in 2023 as the Vice President of Regulatory Affairs and Compliance, marking an exciting new stage for the company in the digital health sector.3
Dr. Roberto Liddi's extensive experience and expertise in regulatory affairs and compliance, combined with his strong academic background, make him a valuable asset in navigating the complex regulatory landscape of the medical device and digital health industries.
