Guidance: NHS population screening: data requests and research
Role and remit of NHS population screening programmes’ research advisory committees.
Role and remit of NHS population screening programmes’ research advisory committees.
Data by National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) showing estimates of birth prevalence of congenital anomalies in England.
These reports detail high consequence infectious disease (HCID) events that are detected during PHE’s epidemic intelligence activities.
Analysis of radiotherapy errors and near misses reported voluntarily by NHS radiotherapy departments.