NCARDRS: postnatal data collection
Postnatal data collection forms for the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).
Documents
Details
Download and complete the form to notify the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) of new antenatal scan results, and send it to the appropriate regional office.
To receive a PDF version of this guidance please email ncardrs@phe.gov.uk.
Updates to this page
Published 9 February 2016Last updated 5 October 2018 + show all updates
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Removed the Zika data collection form because the special arrangements no longer apply and cases should now be notified using the standard forms.
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Replaced regional data collection forms with generic one, added new Zika form.
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First published.