Patrizio Capasso, BSc, MD, DSc.

Regulatory, Quality & Compliance Areas of Expertise 

◎ Clinical Trial Testing Strategy
◎ Risk Assessment and Management
◎ Clinical Trial Expert
◎ Clinical Protocol Design & Development
◎ Principal Investigator
◎ Ethics Committee
◎ Expert Opinion Reports & Testimony
◎ Translational Science
◎ Market Analysis & Forecasts

With approximately 30 years experience in research and clinical practice, Patrizio is a Principal and founding partner of Caduceus Medical Development, Ltd. with its corporate offices located in New Zealand and the United States.

Having trained in the United States, Switzerland and Belgium and obtaining MD degrees in both the US and Switzerland with a Doctorate of Sciences degree from Switzerland, Patrizio has been involved in research and clinical practice since the early 90s. With his training in Medical Oncology, Interventional Oncology, Interventional Radiology and Interventional Neuroradiology, he has been directly involved in preclinical, animal and clinical research projects as a primary investigator and since that time.

Patrizio has held numerous roles with increasing responsibility, in academic medicine in Switzerland, Belgium and most recently the United States where he held the title of Vice Chair and Professor of Radiology and Surgery at the University of Kentucky. Additionally at the University of Kentucky, he held the Chair position of the Institutional Review Board (IRB), overseeing over 7200 clinical and preclinical trials in their initial evaluations, reviews and modifications on an annual basis.

He is a member of numerous national and international clinical, quality and ethical societies, has authored over 65 articles, chapters and books, and is an elected Seldinger Fellow and a Fellow of the Cardiovascular and Interventional Society of Europe.

Patrizio serves as CMDs lead clinical research and medical expert, advising clients on a wide variety of governance, ethical and scientific issues and applictions as well as provides guidance on strategic scientific and research initiatives.

Additionally, from an operational perspective, Patrizio provides a hands-on practical approach to clinical trial protocol design and evaluation, including statistical and ethical parameters; clinical trial data analysis; market review, analysis and strategy development, product design and development, clinical applications and operations as well as GCP compliance.

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