Search results

A user guide for NHS genetic services on the process for requesting genetic data from the National Disease Registration Service (NDRS).

Our strategic plan sets our vision, core business and strategic priorities over the next 12 months. It outlines the strides we are and will continue to make to become a user needs focused service, and to strengthen our stakeholder engagement, including with patients and the public.

The Get Data Out programme uses patient data to improve policy and healthcare in the NHS.

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. 

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).

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

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

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

If we are your sponsoring PSGA member, you must issue Public sector end user licenses to each end user organisation that uses your software.

Sign a contractor licence with a PSGA member.