Master of Medicines Regulatory Affairs

Continuing education for professionals from the pharmaceutical industry

The Master of Medicines Regulatory Affairs targets individuals involved in the regulatory and legislative areas of the pharmaceutical industry, as well as employees in healthcare and biotech companies or in regulatory bodies.

Facilitate sound and transparent regulatory decision-making

Companies face a complex approval process when bringing new products to market. This master's programme provides you with a mix of practice-based competencies, in-depth scientific knowledge and effective negotiation skills.

As a Master of Medicines Regulatory Affairs, you will be able to argue for clinical relevance and scientific legitimacy to ensure a strong, reliable and quality-based storyline.

Courses

Sign up for a single course or enrol in the full master's programme

All courses are designed to fit the busy schedule of regulatory affairs specialists. All courses are lectured in Copenhagen, Denmark. 

Some courses are available every year, while others are available only every second year.

Programme duration

Part-time study for full-time employees

The 60 ECTS credits master’s programme (equivalent to 1 year of full-time study) is designed to be completed within 2 to 6 years of part-time study. Full-time study is not an option, as many courses are available only every second year.