PARLIAMENTARY WRITTEN QUESTION
Congenital Abnormalities: Databases (18 April 2016)
Question Asked
Asked by:
Anna Turley (Labour)
Answer
The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) is operated by Public Health England. NCARDRS has legal permission to collect patient identifiable data without the need for individual consent. As part of this dataset, patient postcodes for individuals resident in England are recorded on the NCARDRS congenital anomaly database. Protection of individual patient data is paramount and release of this data, including postcode data, is strictly controlled.
Answered by:
George Freeman (Conservative)
21 April 2016
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