The MSBase Foundation is an independent not-for-profit organisation that owns and operates the MSBase Registry - a unique international collaborative registry designed for clinicians working in the field of multiple sclerosis (MS) and other neuroimmunological diseases (NIDs), to collect, track, share and evaluate patient outcomes data.

The MSBase Foundation supports Registry members by providing freely available data-entry tools and scientific support. 

The Registry commenced in 2004 and has accumulated over 122,000 patient records from 45 countries, and is the largest organised global repository of longitudinal, 'real-world' MS patient data.

The Registry aims to advance collaborative epidemiological and outcomes research to better understand MS and other NIDs, and to improve healthcare for those living with MS or other NIDs.
A global Board of Directors and a Scientific Leadership Group (SLG) govern The  MSBase Foundation and provide strategic direction to the operations and scientific areas of the Foundation respectively. The Operations Team is responsible for the day-to-day maintenance and management of the Registry. 

The MSBase Foundation

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The MSBase Foundation

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