MS register

Beskrivning

The research group at CNS, KI will participate in the EU project More EUROPA. One of the objectives is to expand the knowledge of real-world data (RWD) and its contribution to the understanding of drug effects and safety. There are further objectives to develop methodological and ethical frameworks for decision-making by authorities, i.e. medicines agencies and HTAs, based on RWD. The research group at CNS will contribute data from the Swedish MS registry and data analysis. In order to increase the amount of data as well as broaden data heterogeneity, more MS registries need to be included (ref project summary).