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National Disease Registration Service (NDRS) analysis and publications focused on cancer in children, teenagers and young adults.
An overview of the cancer awareness programme of activity, how they are run and evaluated.
Discover more about requesting access to National Disease Registration Service (NDRS) data.
Congenital anomalies data collected by the National Congenital Anomalies and Rare Disease Registration Service (NCARDRS).
Explore the 30-day mortality post-Systemic Anti-Cancer Therapy (SACT) case-mix adjusted rates (CMAR) reports. This work is produced by the National Disease Registration Service (NDRS) team, as part of the SACT data programme.
Explore the Systemic Anti-Cancer Therapy (SACT) time to first treatment dashboard. This work is produced by the National Disease Registration Service (NDRS) team, as part of the SACT data programme.
The National Disease Registration Service (NDRS) produces population-based statistics on stage at diagnosis of cancer for patients resident in England.
The National Disease Registration Service (NDRS) produces population-based statistics on incidence of cancer and mortality of cancer for patients resident in England.
Requirements Specification for the National Cancer Registration and Analysis Service (NCRAS) and the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS)
Directions given by the Secretary of State for Health and Social Care to support the transfer of responsibility for the operation and maintenance of the National Disease Registration Service (NDRS).
