National Disease Registration Service Training Events and Refresher Training
Course category National Disease Registration
National Congenital Anomaly and Rare Disease Registration Service (NCARDRS)
This section includes NCARDRS guidance documents and SOPS, including the coding tool. Topics covered include receiving, handling and loading electronic data, the waterfall and assigning batches, as well as processing, registering and cleaning data using CARA. Fetal Anomaly Screening Programme (FASP) guidance is also available. and registered users can access the Genetics forum and Rare Disease forum from here.
