After obtaining Ph.D. in biochemistry in 2013 I began my career in the pharmaceutical industry. Having a strong scientific background, I started working in preclinical drug development. Over several years I expanded my expertise to biocompatibility testing, clinical evaluations and post-market surveillance activities. I gained a broad experience in data retrieval, research methodology, developing research strategies, reviewing of medicinal products dossier and medical devices technical documentation.
For a variety of projects, I was responsible for interactions with regulatory authorities (EU and CIS national competent authorities, notified bodies, FDA) with respect to the scientific and clinical questions, including obtaining scientific advice.