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

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

Ref: PHE publications gateway number: 2014441

PDF, 836 KB, 18 pages

This file may not be suitable for users of assistive technology.

Request an accessible format.

If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email publications@phe.gov.uk. Please tell us what format you need. It will help us if you say what assistive technology you use.

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