Antonio G.

Antonio G. is an experienced professional in regulatory affairs and quality assurance, currently serving as the Associate Director Regulatory Affairs CMC Lead at CEPI since January 2022. Previous roles include Senior Manager and Manager of Regulatory Affairs CMC Development at GSK, where responsibilities encompassed handling change requests, preparing variation submissions across multiple regions, and managing new registrations. Antonio also gained valuable expertise as an International Regulatory Affairs Specialist at Fidia Farmaceutici SPA, focusing on medical device certification and regulatory submissions. Earlier in the career, roles included QP Assistant at Bouty SpA and Quality Assurance Officer at DOC GENERICI SRL, emphasizing quality agreements, SOPs, and regulatory compliance. Antonio holds a Master's degree in Pharmaceutical Technologies and Regulatory Activities from Università degli Studi di Parma and a degree in Pharmacy from the University Magna Graecia of Catanzaro.