David Tome
David is a recognized expert in clinical research and medical device regulation (MDR/IVDR). He is currently President and former Head of Clinical Operations at MDx CRO, a strategic consulting firm that helps MedTech and IVD companies bring their technologies from patent to market in the EU and the U.S. With over 15 years of experience leading clinical operations at industry giants such as Philips and Olympus, he combines his executive role with teaching as a visiting professor at business schools and universities (ESAME, CEU). He specializes in clinical project management, obtaining CE Marking, and developing clinical evaluation reports (CER/PER).
Latest Articles
Blog & Insights
Blog & Insights
Blog & Insights
Blog & Insights
Blog & Insights
Blog & Insights
Importing Investigational Medical Devices into the EU Under the MDR
Last Updated: 2026-07-29
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Blog & Insights
EU Legal Representative for Clinical Investigations Under MDR Article 62(2)
Last Updated: 2026-07-29
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Regulatory Updates
MDCG 2023-4: Medical Device Software (MDSW) – Hardware Combinations
Last Updated: 2026-07-29
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