More than 14 years in pharmaceutical industry including 10 in pharmacovigilance. Responsable for global pharmacovigilance for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical trials, the identification and investigation of safety signals, management of benefit-risk profile for assigned products. Reviews and preparation of safety section for aggregate reports (PADERs, PSURs, PBRERs, DSURs).