The basic documents that define the scope and possibilities of the ReMuS registry are the Informed Consent and the Information on Informed Consent.
The English version is available on the English version of the website.
From the first moments of the ReMuS registry, it was crucial to meet all the necessary ethical parameters of the research. The patient's interests are defended by a specially appointed ethics committee in each of the participating hospitals. The consensus statements of all fifteen committees can be found in the ZIP archive.
Latest data from the registry to 31 December 2023 available in the form of a report here.
The basic data in the register are processed in an anonymised form in a central database based on data as of the last day of June and December. The summary analysis takes the form of a final report as of that date.
We currently publish annual analyses every May on the occasion of World Multiple Sclerosis Day.
