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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.
The Systemic Anti-Cancer Therapy (SACT) data set collects systemic anti-cancer therapy activity from all NHS England providers.
The Rare Disease Data Set (RDDS) is the national standard for collecting rare disease data in the NHS.
Read about the work that the National Disease Registration Service (NDRS) is doing to improve transparency and engage users in our strategies and work planning through the application of our new User-Centred Design (UCD) principles.
Find out how NDRS data can help geneticists to understand Variants of Uncertain Significance (VUS) in cancer susceptibility genes
Find out more about how the NDRS data can be used to support direct care.
Find information for people concerned about their family history of cancer
This document provides supporting information on the National Inherited Cancer Predisposition Register (NICPR) and referrals into the NHS Very High-Risk Breast Screening (VHRS) Programme for clinical genetic teams.
Patient information leaflets on disease registration are available through the National Disease Registration Service (NDRS).
This page contains downloads for the Systemic Anti-Cancer Therapy (SACT) data set version 3.0
