Swiss Multiple Sclerosis Registry

The Swiss Multiple Sclerosis Registry (SMSR) research team focuses on the nationwide, patient-centered longitudinal study for adults with MS in Switzerland. 
We employ a citizen science approach, in which researchers and individuals with MS collaboratively define and investigate relevant questions, always striving to improve the quality of life for those with MS. The SMSR supports flexible participation, from one-time surveys to longitudinal data collection, and enables interdisciplinary research by integrating patient-reported outcomes, clinical data, and epidemiological trends. It is pharma- and industry-independent.

Head: V. von Wyl (E-Mail)
Central Services: J. Piket (E-Mail)