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Summary of 2019 congenital anomaly statistics report released by National Congenital Anomaly and Rare Disease Registration Service, NCARDRS.
This section describes the standard escalation process that will be adopted for NHS trusts who do not comply with the requirements for SACT data submission.
Explore a series of short video giving an overview of the National Disease Registration Service (NDRS) and our work.
This document provides technical guidance to support providers of cancer services, e-Prescribing Managers and IT software developers in the submission of the Systemic Anti-Cancer Therapy (SACT) data set.
Find out more about the National Cancer Registration and Analysis Service (NCRAS) - one of the 2 disease registration services within the National Disease Registration Service (NDRS)
Read about the work that the National Disease Registration Service (NDRS) is doing to consolidate all legacy websites and platforms into a single point of access website.
Discover the work of the Clinical Practice Research Datalink (CPRD) team and the National Disease Registration Service (NDRS) linking primary care patient data across England.
The Simulacrum is a synthetic cancer data set that contains artificial patient-like cancer data to help researchers gain insights into cancer in England.
The partnership on cancer data is set up between NHS England and the systemic anti-cancer therapy (SACT) team at the National Disease Registration Service (NDRS).
