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Opting out of disease registration
Find out how to request for your data to be removed from the National Disease Registration Service (NDRS) registers.
Congenital anomalies data set
Congenital anomalies data collected by the National Congenital Anomalies and Rare Disease Registration Service (NCARDRS).
Trust Guidance for Raising Awareness
This guidance document explains what trust staff should know about cancer registration and what trusts should be doing to increase awareness of cancer registration to patients and healthcare professionals.