Corporate report

Congenital anomaly and rare disease registration service in England: the vision

Public Health England's vision for a single National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).

Documents

Vision for a congenital anomaly and rare disease registration service in England

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Details

This paper outlines the design of a single National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) that will collect data on all congenital anomalies and rare diseases in England.

Published 30 November 2014