FaF:FDTBF_FAF Biopharmaceutics Aspects of Dr - Course Information
FDTBF_FAF Biopharmaceutics Aspects of Drug Evaluation
Faculty of PharmacySpring 2025
- Extent and Intensity
- 1/1/0. 25 credit(s). Type of Completion: zk (examination).
- Guaranteed by
- prof. PharmDr. Mgr. David Vetchý, Ph.D.
Faculty of Pharmacy - Prerequisites (in Czech)
- FAKULTA(FaF)
- Course Enrolment Limitations
- The course is only offered to the students of the study fields the course is directly associated with.
- fields of study / plans the course is directly associated with
- Pharmaceutical Technology (programme FaF, D-FT) (2)
- Pharmaceutical Technology (programme FaF, D-FTA)
- Course objectives
- - Expanding the knowledge of the student focusing on the biopharmaceutical aspects of the evaluation of chemical and biological pharmaceuticals, obtained mainly from world databases containing knowledge from scientific publications especially of foreign research experts and institutions and increasing the ability of the student to process this knowledge into research texts focusing on the content of the study program.
- Learning outcomes
- - Identify the original and generic drug and summarize the important stages of their development - Define generic substitution and describe the degree of similarity of generic medicinal products based on bioequivalence studies - Explain the effects of generic substitution - Define original biological drug and biosimilars - Explain the development and production of biological medicines - Describe the principle and effects of interchangeability of biological drugs - Describe the differences in production and evaluation between a chemical and a biological product
- Syllabus
- 1. Original and generic drug - Development, Production and Evaluation
2. Generic substitution - definition, bioequivalence study, degree of similarity of generic products and impact on generic substitution.
3. Original Biological Medicine and Biosimilar - Development, Production and Evaluation
4. Interchangeability of biological products - view of FDA and EMA, extrapolation of indications, divergence of preparations, proof of consistency of the manufacturing process, processes of change in the production process, immunogenicity
5. Differences in production and evaluation between chemical and biological products
- 1. Original and generic drug - Development, Production and Evaluation
- Teaching methods
- consultation with the teacher
- Assessment methods
- Oral examination
- Language of instruction
- Czech
- Further comments (probably available only in Czech)
- The course can also be completed outside the examination period.
The course is taught each semester. - Teacher's information
- Teaching is by way of consultation.
Current literature will be sent to the student by the guarantor upon request.
- Enrolment Statistics (Spring 2025, recent)
- Permalink: https://is.muni.cz/course/pharm/spring2025/FDTBF_FAF