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Working with data to improve patient experiences, outcomes and save lives

As an NHS organisation, the National Disease Registration Service (NDRS) collects patient data on cancer, congenital anomalies and rare diseases, and provides expert, timely analysis to support clinical teams, academics, charities and policy makers to help plan and improve treatments and healthcare in England.

Do I need to register?

Find out if patients need to register their details with the National Disease Registration Service (NDRS). 

Find out more