Lidija is Associate Manager of Regulatory Affairs at IFPMA. She works on regulatory reliance, as well as matters related to the International Council for Harmonisation (ICH) of Technical Requirements for Pharmaceuticals for Human Use.

Prior to joining IFPMA, Lidija worked in the pharmaceutical company Krka in the marketing department. Having worked as Medical Representative to the Head of Field Force and Training for Southeast Europe, she brings with her experience on how to successfully manage all post-launch activities in the product lifecycle. She holds a Masters in Pharmaceutical Science from the University of Belgrade, Serbia. During her studies, she was involved in scientific work at the Department of Pharmacology.