Programplaner og emneplaner - Student
MAFAR4300 Development and Manufacturing of Medicinal Products Course description
- Course name in Norwegian
- Utvikling og produksjon av legemidler
- Study programme
-
Master´s Programme in Pharmacy
- Weight
- 15.0 ECTS
- Year of study
- 2022/2023
- Curriculum
-
SPRING 2023
- Schedule
- Programme description
- Course history
-
Introduction
Gradert skala A-F.
Required preliminary courses
Ekstern sensor vil sammen med intern sensor sensurere besvarelsene.
Learning outcomes
After completing the course, the student should have the following overall learning outcomes defined in terms of knowledge, skills and general competence:
Knowledge
The student
- can discuss which pharmacodynamic and pharmacokinetic properties form the basis for choosing pharmaceutical candidates and how these properties can be changed and adapted during the process of developing the final new medicinal product
- can explain the structural elucidation and structure-activity relationship of various pharmaceutical candidates
- can discuss especially expedient production and formulation strategies for biologics and radiopharmaceuticals compared with chemical pharmaceuticals
- can explain the requirements that apply to documentation (FDA/EMA) in connection with; a marketing authorisation application for a medicinal product
Skills
The student
- can apply relevant legislation on quality assurance of the manufacturing, storage and distribution of medicinal products, with particular emphasis on radiopharmaceuticals
- can identify and elucidate the typical critical stages of the manufacturing and formulation of biologics compared with chemical pharmaceuticals
- can apply methods for analysis and quality control of radiopharmaceutical ingredients and products, and assess how deviations affect the quality of the final products
General competence
The student
- can critically assess and apply new knowledge about the structure-activity relationship of pharmaceuticals to develop new medicinal products
- can contribute to quality development in the manufacturing of medicinal products
- can contribute to the process of developing a medicinal product until the finished product has been marketed and meet the medical needs of society, at the national and international level, in a sustainable manner
Teaching and learning methods
Statistiske metoder.
Course requirements
- Innføring i vitenskapsteori.
- Autokorrelasjon, Stasjonæritet, Kointegrasjon.
- Auto- og vektorregressive modeller (ARMA, VAR).
- Modellering av volatilitet (ARCH, GARCH).
- Paneldatamodeller.
- Estimering med generalisert momentmetode (GMM).
Assessment
Supervised individual written exam, 5 hours.
Permitted exam materials and equipment
None.
Grading scale
Grade scale A-F.
Examiners
All exams are assessed by an internal and an external examiner.
Overlapping courses
None.