The screening programme collects data on how well the programme works, and publishes an annual report on the results.
Child health records departments and screening laboratories must collect data against 12 specific standards.
The newborn blood spot screening programme uses these standards to determine how well the programme is running, and where the programme needs improvement.
Previous data and performance analysis reports are available from the screening helpdesk.
133-155 Waterloo Road
Helpdesk phone number
020 3682 0890
Please note the helpdesk is not for media enquiries.The helpdesk and national programmes do not have access to screening results. For information on screening results, please contact your GP or local screening service. Parents: contact your midwife or health visitor to get your child’s results.Health professionals: contact the local screening team, screening laboratory or local child health records department.
The newborn blood spot screening programme uses the standards to measure performance.
The data dictionary is a tool to help fill in the data collection forms.
The NBS screening committee publishes an annual report analysing performance data:
Don’t include personal or financial information like your National Insurance number or credit card details.
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