Project Results

The results of the European Register for Multiple Sclerosis (EUReMS) project will be measured against the following set objectives:

• Build on already existing national or regional data collections;
• Involve and combine the expertise of clinicians, researchers and patients organizations;
• Address questions at international level;
• Ultimately contribute to improve access for people with multiple sclerosis (MS) across Europe to evidence-based health care services and offer a cutting-edge research tool to gain further insights into various aspects of MS.