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).

From:
Public Health England
Published
30 November 2014

Documents

Ref: PHE publications gateway number: 2014441

PDF, 836 KB, 18 pages

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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.

Updates to this page

Published 30 November 2014

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