Lamya SAOUSSEN

Lamya holds a Master 2 in European and International Regulatory Affairs and a Master 1 in Pharmaceutical Sciences, both from the University of Lille. She began her career at Baxter International as a Regulatory Affairs Intern, where she managed MA variations, packaging updates, and the review of promotional and non-promotional materials for drugs and medical devices. She was also responsible for updating shortage management plans, drafting internal procedures, and preparing audits. She then joined AstraZeneca as a Regulatory Affairs Apprentice, focusing on national and European registration procedures (national, DCP, MRP, centralized). In this role, she tracked pharmaceutical and clinical variations, validated packaging components, managed early access programs, updated regulatory databases, and carried out regulatory monitoring activities. At Atessia, Lamya contributes to the validation of promotional and non-promotional materials for medicines and medical devices. She also supports registration activities, regulatory monitoring, and ensures compliance with promotional practices and relationships with healthcare professionals in line with applicable regulations (Charters, Anti-Gift Law, Transparency of Links)