MS Data Alliance

In the face of the COVID-19 pandemic, people with multiple sclerosis (MS) and their healthcare providers urgently needed data on the virus’s impact on MS patients. To address this critical need, the MS Data Alliance and the MS International Federation (MSIF) joined forces to create the Global Data Sharing Initiative (GDSI). This groundbreaking collaboration aimed…

The MS Data Alliance (MSDA) is a global multi-stakeholder non-for-profit collaboration that aims to overcome the sociological and technical challenges that arise when scaling-up real-world MS data. The alliance brings together regulatory decision-makers, people with MS/patient societies, data custodians, industry, clinicians and researchers to collaborate in the trustworthy use of real-world health data to accelerate…

Welcome to the MS Data Alliance blog! We are thrilled to have you join us on this journey to accelerate research insights for innovative care and treatment for people with Multiple Sclerosis. The aim of our blog is to provide a platform for experts in the field to share their knowledge and experiences, and for…