Ilaria Zaminga

Ilaria Zaminga is a seasoned professional in pharmacovigilance and regulatory affairs, currently serving as a Pharmacovigilance Manager at Cencora PharmaLex since November 2022. Previous experience includes roles as EU QPPV and Drug Safety Specialist at NTC Pharma from March 2019 to November 2022, and as a Regulatory Affairs Specialist and QPPV Deputy at FederFARMACO from January 2018 to February 2019. Ilaria has also worked as a Pharmacovigilance Consultant at PhAST Consulting S.r.l. and has experience at Alcon, a Novartis company, as a Regulatory Affairs and Safety Officer. Ilaria holds a Second Level Master in Pharmaceutical Technologies and Regulatory Affairs from Università di Pavia, and a Master's Degree in Chemical and Pharmaceutical Technologies from Università degli Studi di Cagliari. Additionally, Ilaria has expertise in adverse event reporting, ICSR management, and compliance with international guidelines.