Paolo Croce is an Associate Director in Regulatory Affairs with over 18 years of experience in the CRO industry, specializing in Clinical, Start-up, and Regulatory environments. Previously, Paolo managed a team of 15 at Chiltern, overseeing study deliverables and resource allocation, and directed various studies at PPD and INC Research. Paolo holds a Ph.D. in Biotechnology from Università degli Studi di Milano and an MSc in Biology from Università degli Studi dell'Insubria. Currently, Paolo leads the Regulatory Liaison team, focusing on activities within the Clinical Trials Information System (CTIS) in compliance with Regulation EU No 536/2014.
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