Agnieszka Sieja

Agnieszka has graduated as MSc. of Biology and Industrial Pharmacy (post-graduated study) at the Jagiellonian University in Krakow. She has almost 15 years of experience in regulatory affairs and CMC, as she used to work at the Institute of Pharmacology at the Polish Academy of Science and at several pharmaceutical companies. Agnieszka joined DADA in 2020, and supports the Regulatory Affairs department. She is a Senior Expert RA/CMC who is responsible for the preparation of quality parts of pharmaceutical dossiers, preparation/evaluation of Active Substance Master Files, and who provides advice on trouble-shooting in relation to development, production and quality issues and due-diligence of Module 3.