Ms. Zibian has a 5-year experience in pharmacovigilance activities; signal detection activities in different data settings, safety signals validation and assessment, benefit-risk evaluation, periodic safety update reports writing, responses to health authorities, case processing in safety databases, individual case medical assessment and review and literature review. Prior to her experience as a senior safety scientist, Ms. Zibian worked in clinical trials management and monitoring and in a Regional Center of Pharmacovigilance in France; mainly in cases medical assessment and risk management activities. Ms. Zibian holds a PharmD from the University of Montpellier and a Master’s degree in clinical research from the University of Lyon.