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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 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).

Find out more about a national survey run by NHS England for people who have had a cancer diagnosis around 18 months after diagnosis.

Orphanet is a unique resource for gathering and improving knowledge on rare diseases.

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

Explore a new dashboard reporting completeness of staging data for cases discussed at multidisciplinary teams (MDTs) submitted by NHS trusts to the National Disease Registration Service (NDRS).

This document provides guidance to clinicians reporting regimen outcomes for non-curative treatments in the systemic anti-cancer therapy (SACT) data set.

Detailed information about how the National Disease Registration Service (NDRS) collects and records data of people with cancer, rare diseases or congenital anomalies.

Find out more about the use of Intensity Modulated Radiotherapy (IMRT) treatment across England.

This tool contains information on whether patients who are eligible for genetic testing after a cancer diagnosis are reported as tested for germline BRCA mutations.