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Croatia Croatia

Head of Medical Affairs and Pharmacovigilance with role of EU QPPV

Medical / Health Care / Pharmaceuticals

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..