Davide Carluccio

Clinical Research professional with over 15 years of experience in global clinical development, spanning Phase I–IV trials, NIS/PASS, and medical device studies. Certified Clinical Project Manager with extensive international monitoring experience (400+ visits) and strong expertise in global Regulatory Affairs (FDA & EMA). Recognized for leading cross-functional teams and mentoring clinical research professionals, he frequently contributes to international congresses as a speaker on clinical operations, regulatory strategy, and trial execution.

Agenda sessions