Drug Regulatory Affairs

The programme offers an interdisciplinary and international academic education combining the fields of pharmacy, law and medicine in a dynamic and socially relevant area. It is focused on practice-oriented postgraduate training and provides you with up-to-date knowledge in regulatory affairs: medicinal products, medical devices, life cycle, quality-safety-efficacy, document management, market access, decision making, etc. Connect with more than 100 passionate senior experts from health authorities, pharmaceutical companies, industry associations, academia, and expand your professional network Get trained on a comprehensive range of regulatory science and healthcare topics Learn how science and regulatory competence can create additional value for patients, healthcare systems, and society Expand your expertise and accelerate your professional development with excellent teaching from our dedicated team of experts Receive the academic degree Master of Drug Regulatory Affairs (MDRA.) Modules 1 to 12, content Dedicated team of experts/lecturers