North American Registry for Care and Research in MS - NARCRMS

Brief Description Of Study

NARCRMS is a national database that collects patient and physician-based information on MS and will bring together information and data collected in multiple registries and databases across the U.S. and Canada. We expect that data collected consistently over long periods of time, when carefully studied, will 1) produce new clues to the causes of MS, 2) significantly enhance the ability of physicians, other clinicians, and patients to manage symptoms, and 3) potentially affect the progression of the disorder, and perhaps lead to the eventual eradication of MS.

Clinical Study Identifier: N/A

Contact research investigator to learn more about this study by filling out the form below.


To: Research Study Investigator
Subject: I am interested in participating in your Research Study
Dear Investigator,
I'm interested in learning more about and participating in your research study named: North American Registry for Care and Research in MS - NARCRMS
I am hoping to hear back from you and discuss details of the study

By clicking "Contact Research Team", your contact information will be sent directly to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.