Alenka Dražumerič

Master's in Regulatory Affairs
Director of Regulatory Affairs

illev Pharma East has a highly educated and dedicated team of international experts with many years of experience in Pharmaceutical industry.

Alenka has more than 20 years of experience working in the pharmaceutical industry on various regulatory affairs positions. She has a Bachelor’s in Chemical Process Technology and holdsa a Master’s Degree in Regulatory Affairs by TOPRA (The Organisation for Professionals in Regulatory Affairs). 

For 15 years, she has worked as Regulatory Affairs Manager for generic company Lek Pharmaceuticals, a part of Sandoz, Novartis group on various global projects. She was responsible for all regulatory matters relating to the dossiers’ Modules 2 to 5 of the company’s various human generic products in Europe, Canada, USA (United States of America), LATAM (Latin America), and ROW (Rest-of-the World) countries. She mostly worked on development projects on the CMC drug product part of the dossier. 

In 2015, Alenka joined Medis pharmaceuticals company, and  worked in various regulatory affairs positions taking care of European regulatory issues in the development of herbal products, generics, and medical devices. 


Since 2021, Alenka has worked in Billev Pharma East as the Director of Regulatory Affairs.


Alenka likes spending her free time with family and friends in nature.