Research interests: cellular biotechnologies and drug development (drug design). He has been an expert in the implementation of the international quality standard in the field of good practices GxP (GLP, GMP, GPP, GDP, etc.) and ISO standards for more than 10 years. He is the author of about 70 scientific papers in this field, of which 12 publications are indexed in the Scopus and Web of Science Core Collection - Clarivate databases. She trained at the Veterinary and Pharmaceutical University of Brno (Czech Republic) at the Department of Technology dosage forms and Westminster university in London. Participated in the development of liquid and solid dosage forms based on the original synthetic substance. He is proficient in technologies of extraction processes (supercritical carbon dioxide extraction, extraction with organic solvents), methods of cell breeding, animal reproduction, skills in developing technological documentation and conducting validation/qualification work. Participated in PCF programs for the development of anti-infectious drugs (MIIR RK) and the development of effective technologies, management of the breeding process and conservation of the gene pool in horse breeding (Ministry of Agriculture of the Republic of Kazakhstan). At the moment, she is supervising of master's studies.