is a pharmacist by education, with a Diploma from the National Pharmaceutical University, a postgraduate certificate in Economics and Management in Pharmacy, and a postgraduate certificate in Regulatory Affairs from the University of Hertfordshire.
She has over 15 years of experience in the pharmaceutical industry, working in quality assurance, as an expert for a national state authority, and in regulatory affairs roles within various brand and generic international companies, and consultancy firms.
Her expertise spans dossier preparation and assessment, coordination of regulatory submissions, development and global customisation of regulatory governance documents, managing communication with national competent authorities, regulatory information systems (RIM) onboarding, and compliance audits. In addition, she provides specialised services in regulatory intelligence, due diligence, risk assessment, and regulatory strategies for emerging markets, including new submissions, life-cycle management, site and marketing authorization transfers, localisation projects.