Denmark provides several national registries and disease / intervention registries. One of the unique benefits that Denmark provides is the speed of access. In best case scenario, data can be provided in 2 months. One of the drawbacks, is that the research must be carried out in Denmark.
Here are similar RWD overviews for:
If you are interest to learn more about the potential utility of registries, don’t miss this upcoming webinar:
- 24th of November: Utilizing Finnish nationwide RWD to create an external control arm to a clinical trial
We recommend this article that provides a good overview of the Danish real-world data:
Schmidt, Morten, Sigrun Alba Johannesdottir Schmidt, Kasper Adelborg, Jens Sundbøll, Kristina Laugesen, Vera Ehrenstein, and Henrik Toft Sørensen. “The Danish Health Care System and Epidemiological Research: From Health Care Contacts to Database Records.” Clinical Epidemiology 11 (July 12, 2019): 563–91. https://doi.org/10.2147/CLEP.S179083.
Selection of national registries in Denmark and associated publications: