Francesco Quattrin

Francesco Quattrin is an experienced Regulatory Affairs Specialist currently employed at LEO Pharma since July 2022, where responsibilities include managing local regulatory activities related to clinical trials and marketing authorization applications, as well as providing strategic regulatory insights and fostering relationships with health authorities. Prior to this, Francesco served as a Regulatory Affairs Associate at Bruno Farmaceutici S.p.A. from March 2020 to July 2022, focusing on regulatory documentation submission per EU regulations and handling promotional material submissions. Francesco's career also includes significant roles at AIFA Agenzia Italiana del farmaco, contributing to regulatory assessments and clinical trial management, alongside earlier experience as a pharmacist at Farmacia Bartalotta. Educational background includes Master's degrees in Quality Systems GXP and ISO, and in Clinical and Preclinical Drug Development from Università Cattolica del Sacro Cuore.