Master's project
During the master's project, you will apply knowledge about scientific methods for the solution of a scientific problem within the field of medicines regulatory science.
The master's project in Medicines Regulatory Affairs typically comprises a literature study on a selected topic, selection and description of relevant regulations, guidelines literature and scientifically based documentation, a discussion of the scientific based documentation related to the relevant literature, regulations and guidelines as well as a conclusion on the results of the project.
The project topic can be an investigation of a particular regulatory case, implementation of a regulatory activity in a company, or a study of a particular regulatory problem. In any event, the selected subject should be put into the context of a broad regulatory perspective.
Course details
| Duration: | Individual agreement, approximately 332 hours of work for 12 ECTS |
| Dates: | Dates for start and hand-in must be stated in the agreement |
| Frequency: | Available every year |
| Place: | University of Copenhagen, Copenhagen, Denmark |
| Course fee: | EU/EEA citizens: 15.000 DKK Non-EU/EEA citizens: 21.000 DKK Terms and conditions |
| Level and credit: | Part-time master's level; 12 ECTS |
| Examination date: | Individual agreement |
| Application deadline: | Rolling admission |
| Admission: | Only available for students enrolled on Master of Medicines Regulatory Affairs |
The opening of the application period is announced via the programme newsletter.