Registry research consists of epidemiological and observational studies. The anonymised and encrypted unique personal identification number (CPR) is linked to other population-based national registers, thereby making it possible to study data on the entire population and not just in small groups.
The Danish MS Registry also participates in different international research collaborations
All projects must be reviewed and approved by the steering committee of the Danish MS Registry.
Management team and researchers in the Danish Multiple Sclerosis Registry