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.
|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.