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National data on the prevalence of spinal muscular atrophy type 1 (SMA1) from the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS)

The latest 2019 congenital anomaly statistics report released by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS)

This user guide provides information about the purpose of the CancerStats2 (CS2) data platform, an overview of what data and interactive reports are available and how the data should be used.

The Final Seniority Figure (FSF) is an earnings benchmark used to determine the level of seniority payment that individual GPs are entitled to each year. The seniority payment that is awarded to an individual GP is dependent on their years of reckonable service in the NHS and their qualifying income...

Guidance on using the Rapid Cancer Registration Data (RCRD) to measure progress against the 75% staging ambition.

Explore all annual reports released by the National Congenital Conditions and Rare Diseases Registration Service (NCARDRS) containing information on congenital conditions detected in babies delivered between 2015 - 2021.

Find out more about the National Congenital Condition and Rare Disease Registration Service (NCARDRS) part of the National Disease Registration Service (NDRS).

Discover how the National Disease Registration Service (NDRS) supports national screening programmes in the NHS.

Find out more about our work with the NHS Fetal Anomaly Screening Programme (FASP)

Find out more about our work to support the NHS Newborn Blood Spot Screening Programme (NHS NBS), including our involvement with newborn screening evaluation.