Dr. Anna Dabizha

• compiled documentation for a registration of a new dosage form or re-registration in the GFC; • developed new drug analysis’ methods • provided technical expertise in the design and implementation of a quality control program • was responsible for the quality of each product that left the production line • developed of physical and chemical control methods of validation • managed all the processes in production and the labs to make sure Standard Operating Procedures are followed

• worked with variety of analytical tools and techniques, including chromatography and spectroscopy, standard characterization techniques, operated with equipment • interpreted and processed data for reports • organized and performed experiments for the optimization of adsorption processes