7M10117 Pharmacy

Цель: Provide training of competitive specialists with advanced knowledge and skills, able to generate new knowledge in order to ensure the quality, safety and efficiency of the development and circulation of drugs, in accordance with the current legislation of the Republic of Kazakhstan and Good Pharmaceutical Practices.

Предметы на ЕНТ: Management and economics of pharmacy and drug technology и Pharmaceutical chemistry and pharmacognosy

Educational program

Provide training of competitive specialists with advanced knowledge and skills, able to generate new knowledge in order to ensure the quality, safety and efficiency of the development and circulation of drugs, in accordance with the current legislation of the Republic of Kazakhstan and Good Pharmaceutical Practices.

Upon completion of this program, students will be able to:
1. Identify, demonstrate developing knowledge and understanding of an interdisciplinary nature, describe and analyze professional information in the field of circulation of medicines and medical devices in organizing the work of various pharmaceutical organizations in the production, control, registration and distribution of goods, and providing pharmaceutical assistance to the population and organizations using information and communication technologies.
2. Analyze and evaluate existing concepts, theories, interpret approaches to the analysis of processes and phenomena; introduce new approaches within the framework of their qualifications when consulting patients and doctors on the provision of pharmaceutical care, the rational use of medicines and medical devices, the conditions for their proper storage, the choice of dosage forms, the cost of therapy; demonstrate the ability to professionally solve the main tasks and systematize information on maintaining clinical and pharmaceutical documentation.
3. Apply knowledge on the organization, planning and control of the functioning of subjects in the health care system and the pharmaceutical industry, taking into account the requirements of regulatory documents and international good practices of GXP in the field of circulation of medicines and medical devices to provide timely and high-quality pharmaceutical care to the population and medical organizations.
4. Analyze and understand the regulation of the organization, management and sale of medicinal products, the formation and rational use of inventory of pharmaceutical organizations for wholesale and retail sales to the population and organizations using innovative communication tools.
5. Generalize, analyze and differentiate General issues of clinical pharmacology and clinical and pharmacological characteristics of individual groups and drugs, clinical aspects of pharmacokinetics and pharmacodynamics; evaluation of drug use, pharmacovigilance issues (GVP), regulation of drug provision in medical institutions in compliance with the principles of rational pharmacotherapy for certain diseases.
6. Analyze and differentiate the regulatory and technical documentation of the process of manufacturing and manufacturing of medicines and medical devices; systematize, summarize research results and select the best methods and technologies for their production in accordance with the requirements of the GMP and GLP good manufacturing practice standard.
7. Identify active and related substances in natural raw materials, quality control of pharmaceutical substances, reference materials, excipients and materials, medicinal plant raw materials, as well as medicines and medical devices at all stages of collection, storage and technological process in accordance with current legislation and good GXP pharmaceutical practices, possession of modern physical, physico-chemical and chemical methods of their analysis.
8. Analyze, systematize and generalize the research goals and the selection of objects of chemical and Toxicological examination in accordance with the current legislation of the Republic of Kazakhstan, form judgments when registering the results of the examination.
9. Demonstrate a commitment to the highest standards of professional responsibility and integrity; and adhere to ethical principles in all professional interactions with patients, families, colleagues, and society at large. Apply knowledge of the principles and methods of forming a healthy lifestyle of a person and family, a set of factors that determine health and disease for the purpose of prevention.
10. Demonstrate communication skills and learning skills, continuously improve professional knowledge and skills, demonstrate the formation of judgments and skills of scientific research, the desire to transfer knowledge to others.

Master's degree educational programs

Persons entering the master’s degree or residency:
when applying to organizations of university and postgraduate education:
1) an application addressed to the head of the organization of higher and postgraduate education in any form;
2) document on higher education (original);
3) certificate of completion of the internship (for admission to residency);
4) identity document (required for personal identification);
5) six photographs 3x4 centimeters in size;
6) a medical certificate in the f

Curriculum

СЕМЕСТР 1

Foreign language (professional)-5 ECTS
Psychology of management-3 ECTS
Organization and Planning of Scientific Research in Pharmacy (in eng)-5 ECTS
Concept, principles and functions of pharmaceutical distribution-5 ECTS
Strategic Management-5 ECTS
Data Analysis Methods: Planning and Preparation-5 ECTS
Quality management of medical care-5 ECTS
Safety of medicines and pharmacovigilance-5 ECTS
Statistical methods of analysis in clinical practice-5 ECTS
Proper control of manufacturing processes and laboratory preparation of drugs-5 ECTS
Chemistry and technology of biologically active substances from plant materials-5 ECTS
Experimental Design in Drug Development-5 ECTS
Fundamentals of Bionanotechnology in Pharmacy-5 ECTS
Nanotechnology and Nanomaterials-5 ECTS
Design of experiments in nanopharmacy-5 ECTS
Research Seminar-1 ECTS
Dissertation Writing-1 ECTS

СЕМЕСТР 2

History and philosophy of science-3 ECTS
Pedagogy of higher education-5 ECTS
Pedagogical-4 ECTS
Drug delivery systems-5 ECTS
Quality management in pharmaceutical organizations-5 ECTS
Epidemiology-5 ECTS
Research Seminar-1 ECTS
Dissertation Writing-2 ECTS

СЕМЕСТР 3

Clinical pharmacology and pharmacotherapy-5 ECTS
Standardization of drugs-5 ECTS
Research-4 ECTS
Counterfeit medicines and their regulation-5 ECTS
Marketing Research in Pharmacy-5 ECTS
Development of a drug registration dossier-5 ECTS
Ensuring rational pharmacotherapy-5 ECTS
Ensuring pharmaceutical care of the population-5 ECTS
Organization of clinical and preclinical trials of medicines GLP, GCP-5 ECTS
The concept of drug quality assurance-5 ECTS
Biopreparation manufacturing technology-5 ECTS
Spectroscopic analysis of the drugs-5 ECTS
Nanotoxicology-5 ECTS
From nanoparticles to biomolecules-5 ECTS
Nanopharmacy-5 ECTS
Dissertation Writing-1 ECTS

СЕМЕСТР 4

Research-4 ECTS
Research Seminar-1 ECTS
Dissertation Writing-10 ECTS
Scientific Internship-3 ECTS
Publication in the Proceedings of International Conferences-4 ECTS
Final Attestation-8 ECTS

Employment

- Medical education institutions (colleges) - Research centers - Production and manufacture of medicines; - Sales manager of medicines; - Provision of conditions for storage and transportation of medicines; - Participation in carrying out procedures related to the circulation of medicines; - Participation in quality control of medicines; - ensuring information about medicinal products within the limits established by the current legislation; - carrying out sanitary and educational work with the population; - Formation of motivation of citizens to maintain health; - Participation in providing assistance to the population in emergency situations at the stages of medical evacuation, including the organization of the supply of medicines and medical devices.

Contacts