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Established in 2010, the National Registry of Rare Kidney Diseases (RaDaR) is an initiative by the UK Kidney Association. Its purpose is to gather longitudinal data on patients diagnosed with specific rare kidney diseases. With 33,000 patients enrolled from 109 sites throughout the UK, RaDaR stands as the largest rare kidney disease registry globally.

The Danish Multiple Sclerosis Registry is one of the oldest and largest MS registries globally, housing nationwide prospective data on all Danish residents diagnosed with MS from 1948 to the present. The registry undergoes a new build approximately every month, during which data are extracted, checked, and cleaned.

We are excited to announce the recent enhancements and upgrades in our tutorial - How to Create Collections on B.R.I.D.G.E. TO DATA^®. This updated video demonstrates how to narrow down search results, save collections for future use, and leverage new features for even better profile comparisons.