Learning outcomes

The programme will provide you with a mix of practice-based competencies, in-depth scientific knowledge and effective negotiation skills.

A comprehensive understanding of the regulatory process enables a more strategic and tactic approach to be taken to ensure innovation progress while maintaining product safety in order to obtain a sound and speedy marketing authorisation.

Enrol in the master’s programme and:

  • Achieve a thorough insight into the regulatory process at all stages during drug development;
  • Become competent in analysing, predicting and advising on drug regulations and directives;
  • Learn to critically examine legislation in regulatory science;
  • Get an overview of the differences in regulatory demands globally;
  • Understand how to organise the regulatory work across the classic safety, clinical and quality disciplines to prevent delays in the innovation process.