National Congenital Anomaly Register

Our President, Tim Overton currently chairs  the Expert Clinical and Scientific Advisory Panel  for the National Congenital Anomalies and Rare Disease Registration Service which oversees the activities of the National Congenital Anomaly Register. There are likely to be some changes in the type of data collected by the register and further details will be available soon. Feel free to contact Tim if you wish to raise any concerns.


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News

09/08/2017
CONSULTANT OBSTETRICIANS needed to interview: The Montgomery v Lanarkshire Health ruling
13/06/2017
Committee elections
15/05/2017
Management of prenatally detected third trimester unilateral hydronephrosis
11/05/2017
The Non-Invasive Prenatal Test: Warwick Policy Briefing
11/05/2017
Universal late pregnancy ultrasound screening in nulliparous women
12/04/2017
The NHS Fetal Anomaly Screening Programme (FASP)

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