Bruno Strappa

Project Associate

Bruno holds a M. Sc. in Bioengineering. He manages a portfolio of regulatory compliance projects with both large bio-pharmaceutical firms and medical devices / IVD startups. He has previously worked at a medical device start-up managing an interdisciplinary team, developing the regulatory approach and related Technical Documentation. Bruno has extensive experience in the setup of regulatory strategies and related technical / QMS documentation for EU and US approval, especially for drug device combination and for IVD products where the concepts of scientific validity and analytical performance are central. Bruno is fluent in English and Spanish.