AZZEDINE SAICHE

Azzedine Saiche has extensive experience in regulatory affairs within the pharmaceutical industry. From January 2015 to April 2020, Azzedine served as Regulatory Affairs Manager at both ProductLife Group and Lundbeck, focusing on international submissions for drug registrations, variations, and renewals across diverse regions including Asia, Latin America, Africa, and the Middle East. Azzedine transitioned to Servier in April 2020 as a Regulatory Affairs Expert - Projects Coordinator, managing worldwide regulatory processes for renewals and safety variations. Additional experience includes a role at GSK as Regulatory Affairs Manager, where Azzedine handled submission dossier preparation and compliance, and a position at BIOGARAN as a CMC Consultant for generics. Azzedine began regulatory work at QUIMDIS S.A.S as a Regulatory Affairs Officer, developing strategies for raw materials and ensuring compliance with European regulations. Azzedine holds an education background from Université de Rennes 1-Faculté de Pharmacie.