PhD courses
Speciality Code:
8D07201
Speciality Name:
Pharmaceutical Manufacturing Technology
Faculty:
Chemistry and Chemical Technology
Qualification:
- Scientific and pedagogical direction - Doctor of Philosophy (PhD)
- Model of graduating student
- Mandatory disciplines
- Elective disciplines
- Professional
1. Possess knowledge and modern innovative technologies for carrying out effective scientific and pedagogical activities, solving problems in the field of organizing the production of original medicines based on natural and synthetic raw materials, taking into account economic and environmental factors, their pharmacokinetics and bioequivalence.
2. Carry out targeted 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. Demonstrate 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. Organize 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. Organize 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. Analyze and control 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. Organize 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).
8. Apply 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.
9. Carries out academic, research, scientific-methodological and social activities in the Higher Educational Institution.
2. Carry out targeted 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. Demonstrate 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. Organize 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. Organize 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. Analyze and control 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. Organize 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).
8. Apply 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.
9. Carries out academic, research, scientific-methodological and social activities in the Higher Educational Institution.
Data for 2022-2025 years
Data for 2022-2025 years
Data for 2022-2025 years