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THE CZECH REMUS REGISTRY – UNIQUE SOURCE OF OBJECTIVE DATA FOR THE REALISATION OF RESEARCH PROJECTS AT A REGIONAL, EUROPEAN AND INTERNATIONAL LEVEL

With regard to the size of the Czech Republic and to the good set-up of the project’s infrastructure as well as networked healthcare, ReMuS is a model example of a functioning national registry providing a representative sample of data about multiple sclerosis in the European Region. 

The data collection itself is based on the Informed Consent of each patient. The basic data is anonymously processed in the central database twice a year. The summary analysis has the form of a final report, which is available for the public HERE.

However, due to its scope, the registry enables much wider use for analysis and studies about the disease, about its development, influence of different environmental factors and effect of the treatment. 

If you are interested in cooperation in research or clinical studies, please contact us: This email address is being protected from spambots. You need JavaScript enabled to view it..