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Pharmaceutical Policy and Management

Study Course Description

Course Description Statuss:Approved
Course Description Version:4.00
Study Course Accepted:02.02.2024 12:29:44
Study Course Information
Course Code:VVDG_008LQF level:Level 7
Credit Points:2.00ECTS:3.00
Branch of Science:Basic Sciences of Medicine, including Pharmacy; Social PharmacyTarget Audience:Health Management
Study Course Supervisor
Course Supervisor:Daiga Behmane
Study Course Implementer
Structural Unit:Faculty of Social Sciences
The Head of Structural Unit:
Contacts:Dzirciema street 16, Rīga, szfatrsu[pnkts]lv
Study Course Planning
Full-Time - Semester No.1
Lectures (count)6Lecture Length (academic hours)2Total Contact Hours of Lectures12
Classes (count)6Class Length (academic hours)2Total Contact Hours of Classes12
Total Contact Hours24
Study course description
Preliminary Knowledge:
None required.
Objective:
The student gains knowledge about pharmaceutical policy and regulation of pharmaceutical systems in the European Union, aspects of the pharmaceutical market, its regulation, globalisation trends, the role of the government in the regulation of the pharmaceutical market.
Topic Layout (Full-Time)
No.TopicType of ImplementationNumberVenue
1Pharmaceutical market: characteristics, globalisation trends, market segments, market operatorsLectures1.00auditorium
2Pharmaceutical market analysisClasses1.00auditorium
3Characteristics and regulation of the pharmaceutical industryLectures1.00auditorium
4Analysis of laws and regulations governing pharmacyClasses1.00auditorium
5National medicinal product policy and principles for the development thereofLectures1.00auditorium
6Comparative analysis and evaluation of medicinal product policyClasses1.00auditorium
7Objectives, tasks, structural principles of reimbursement systemsLectures1.00auditorium
8Analysis of reimbursement systemsClasses1.00auditorium
9Medicinal product cost control measures, supply and demand aspects, price formation in the medicinal product marketLectures1.00auditorium
10Comparative analysis of the costs of medicinal productsClasses1.00auditorium
11Principles and application of economic evaluation of medicinal productsLectures1.00auditorium
12Economic evaluation of medicinal productsClasses1.00auditorium
Assessment
Unaided Work:
Analysis of problem situations. Data analysis and evaluation. Analysis of policy documents.
Assessment Criteria:
Activity during the interactive lectures. Solving situational tasks in classes. Presentation of independent work. Correct answers in the written test.
Final Examination (Full-Time):Exam
Final Examination (Part-Time):
Learning Outcomes
Knowledge:To understand the principles of pharmaceutical policy-making and the role of the pharmaceutical system in national social security systems, the content of pharmaceutical policy. To understand the aims and objectives of pharmaceutical policy. To understand the global aspects, development trends and challenges of the pharmaceutical market and the need to balance the goals of the pharmaceutical industry and public health. To understand the regulation of the pharmaceutical industry at the European Union and national level. To understand the regulatory aspects of the pharmaceutical market and the role of the government in regulation. To understand the pricing aspects of medicinal products. To understand the factors affecting the cost of medicinal products.
Skills:To determine the aims and objectives of pharmaceutical systems. To analyse the performance of pharmaceutical systems according to their key performance indicators. To analyse the performance indicators of the pharmaceutical system. To analyse the elements of the pharmaceutical market, development trends. To compare the development of the medicinal product market in different countries. To identify the factors influencing the cost of medicinal products and how they can be limited. To define the roles and design principles of hospital medicinal product procurement systems. To define the roles and design principles of medicinal product reimbursement systems. To identify issues in pharmaceutical systems and justify them for research. To assess the performance of pharmaceutical systems against their target indicators.
Competencies:To develop the aims, objectives of pharmaceutical policy. To determine the tasks of pharmaceutical system development. To contribute to the development of laws and regulations governing the pharmaceutical system. To analyse the medicinal product market. To establish medicinal product procurement systems at the level of a medical treatment institution. To make proposals for regulating the prices of medicinal products. To make proposals for action on the factors affecting the cost of medicinal products. To participate in research projects in the pharmaceutical field.
Bibliography
No.Reference
Required Reading
1E.Mossialos, M.Mrazek, T.Walley „Regulating Pharmaceuticals in Europe: Striving for Efficiency, Equity and Quality, European Observatory on Health Systems and Policies, 2004 (akceptējams izdevums)
2Drugs and money: Prices, affordability and cost containment, 7th edition, 2003, WHO (akceptējams izdevums)
Additional Reading
1Priority Medicines for Europe and the World update Report, 2013
Other Information Sources
1http://ec.europa.eu/enterprise/sectors/pharmaceuticals/
2www.who.int/medicines/
3http://whocc.goeg.at