Maria Filancia is a Scientific Administrator at the European Medicines Agency since 2015 working in market surveillance work stream of the service Manufacturing Quality and Supply Chain Integrity. She coordinates the assessment notifications related to quality defects, rapid alerts, statement of non-compliance with GMP and falsified medicines.
Ms Filancia has completed Master's in Biotechnologies for Human Health and Bachelor's degree in Sanitary Biotechnology from University of Siena, Italy.
Previously, she has worked with Health Products Regulatory Authority (HPRA, Ireland) as a Scientific Officer in the Sampling and Analysis work stream of Market Compliance department. She has also worked as a quality control analyst for industry (MSD, Ireland) and third party laboratory (CTP Chem, Italy).