Master of Medicines Regulatory Affairs (MRA)

SUMMARY

Experts in Regulatory Affairs are essential for companies facing an increasingly complex approval process for bringing new products to market. Master of Medicines Regulatory Affairs educates regulatory experts to help secure their organisation a safe, coherent, and successful regulatory process.

Master of Medicines Regulatory Affairs is offered by the University of Copenhagen in collaboration with Atrium, and brings together the best from both academia, industry, and authorities which support the Master’s ability to attract international experts and scientists in medicines regulatory affairs and regulatory science.

Atrium is part of the Master of Medicines Regulatory Affairs because we want to help ensure ongoing learning and development for Regulatory Affairs professionals. Our collaboration with University of Copenhagen links academia and industry to ensure valuable learning experiences that help you advance professionally.

Courses offered in collaboration between Atrium and University of Copenhagen

5 of the courses at the Master of Medicines Regulatory Affairs are offered by Atrium in collaboration with the University of Copenhagen. These 5 courses are practice-based courses in Regulatory Affairs. The remaining Master courses are offered only by the University of Copenhagen.

The courses offered in collaboration between Atrium and University of Copenhagen can be taken by both Master students, by students taking the Atrium Diploma in Regulatory Affairs, and by single course students.

You apply for enrollment at the Master of Medicines Regulatory Affairs at the University of Copenhagen. Please go to www.mra.ku.dk to learn more about the Master of Medicines Regulatory Affairs and to see admission criteria, application procedure, and tuition fees.