• Scientific and pedagogical direction - Doctor of Philosophy (PhD)

1. Possesses knowledge and modern innovative technologies for solving tasks in the field of organization, creation, production, and standardization of original medicines based on natural and synthetic raw materials, taking into account economic and environmental factors, their pharmacokinetics, and bioequivalence.
2. Is capable of directed design of new pharmaceutical drugs based on computer and mathematical modeling, macromolecular polymer design, development of nanopharmaceuticals; comprehensive and complete identification of active pharmaceutical ingredients and drugs based on highly effective physicochemical methods.
3. Demonstrates the ability to organize, plan, and manage the activities of pharmaceutical organizations and enterprises in accordance with the current legislation of the Republic of Kazakhstan in the field of healthcare, Good Pharmaceutical Practices GxP (GMP, GLP, GSP, GDP, GPP), and principles of modern marketing and management.
4. Organizes work to ensure and control the quality, safety, and efficacy of medicines, addressing identified violations of pharmaceutical activities in the production, storage, transportation, acceptance, and sale of medicines and medical devices in accordance with the current legislation of the Republic of Kazakhstan in the field of healthcare and Good Pharmaceutical Practices (GxP).
5. Organizes systems of external and internal audits of entities engaged in pharmaceutical activities, demonstrating knowledge of Good Pharmaceutical Practices (GxP) and the current legislation of the Republic of Kazakhstan.
6. Analyzes and controls documentation related to the handling of medicines at all stages of their lifecycle: standard operating procedures, instructions, contracts, records, reports, test protocols, and other data.
7. Organizes a system for monitoring, analyzing, and evaluating information on the safety of medicines in accordance with the current legislation of the Republic of Kazakhstan in the field of healthcare and Good Pharmacovigilance Practices (GVP), using various methods to assess the efficacy and safety of medicines during monitoring of their adverse effects, organizing the collection and analysis of information on the safety of medicines.
8. Applies modern information and computer technologies in the collection, storage, processing, analysis, and transmission of professional information in the process of scientific and pedagogical activities at the university, as well as in production-technological, design-engineering, scientific-research, and organizational-management activities.