Master's project
This course is a part of
The topic of the master's project topic in Medicines Regulatory Affairs, 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.
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.
Details about Master's Project
Content
Project dates
Dates for start and hand-in must be stated in the agreement.
Duration
Individual agreement, approximately 332 hours of work for 12 ECTS.
Examination date
Individual agreement.
Please find the exam dates in the exam plan.
You can find further information about the course and the exam in the course curriculum.
Tuition Fees
EU/EEA citizens: 15,900 DKK*
Non-EU/EEA citizens: 23,100 DKK
*Citizens of the EU, EEA or Switzerland is entitled to a subsidised tuition fee, due to EU legislation, hence the difference in price.
Admission
The Master's project is not available for single course students.
Read more about the Master of Medicines Regulatory Affairs and apply for the programme here: Master of Medicines Regulatory Affairs.
Place
University of Copenhagen
Department of Pharmacy/
Department of Drug Design and Pharmacology
Universitetsparken 2
2100 Copenhagen
Denmark
Contact
Annette Villumsen
Study Administration Officer
Tel.: +45 35 33 60 66