Find your way through EMA

We monitor and register applications from pharmaceutical companies to the European Medicines Agency (EMA). Both applications for marketing licences for new pharmaceuticals, as well as applications for major changes to existing marketing authorisations such as extensions of indications and other extensions.

It can be difficult to understand the regulatory procedures in the European Medicines Agency (EMA). Therefore, as a service for our stakeholders we have prepared a guide to the European Medicines Agency (EMA), which we call "Find your way through the European Medicines Agency (EMA)” (only available in Danish). You can read the complete guide or use it for reference.