/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: TatjanaAjhlerDuretek https://cdn.slidesharecdn.com/profile-photo-TatjanaAjhlerDuretek-48x48.jpg?cb=1618171481 I have been working in pharmaceutical industry since 1994. mostly in Regulatory Affairs department and have broad experience in drug regulatory issues in EU and USA. I joined Belupo team in 2005 and became the qualified person for pharmacovigilance in 2006. I manage the team responsible for preparing clinical documentation for national and European procedures and coordinating clinical studies for the generic development projects. As QPPV I am involved in the development of Pharmacovigilance department and setting up of compliant Belupo’s pharmacovigilance system..