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Martina Kaic has over 12 years of experience in regulatory affairs and pharmacovigilance. Martina has worked at Medis since 2016, initially as the Regulatory and Pharmacovigilance Manager and later as the Head of Regulatory Affairs for EU Countries. Martina also served as the Deputy EEA QPPV and the local QPPV in Croatia. Prior to that, they worked at Novo Nordisk as a Regulatory Affairs professional from 2014 to 2016. Before joining Novo Nordisk, they were a Regulatory & Pharmacovigilance Expert at Medis Adria d.o.o. from 2009 to 2014.

Martina Kaic commenced their education at V Gymnasium in 1990, where they studied until 1994. Martina then pursued their academic career at the Faculty of Pharmacy and Biochemistry from 1994 to 1999, focusing on the field of Pharmacy. No degree name was provided for their time at the Faculty of Pharmacy and Biochemistry.