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STFYAYB provides information about the screening tests offered during and after pregnancy.
This short animation shows the screening tests offered during pregnancy…
Public Health England (PHE) created this information on behalf of the NHS.…
This information was created on behalf of the NHS. In this information,…
Guidance for local NHS screening services on how to order and access printed and digital population screening leaflets.
These 8 easy read guides explain the screening tests offered during and after pregnancy for people with learning disabilities.
The processes for managing safety incidents in the NHS screening programmes.
Information on the programme, including the screening tests, commissioning, quality assurance, education and training.
Policy and standards for antenatal laboratories working with the NHS sickle cell and thalassaemia (SCT) screening programme.
Resources to support screening professionals in their initial training and continuing professional development (CPD).
Information for pregnant women who are offered a chorionic villus sampling (CVS) or amniocentesis diagnostic test.
Information for pregnant women to understand what it means to be a beta thalassaemia carrier.
Guidance for healthcare professionals covering the pathway for sickle cell and thalassaemia screening.
Screening standards for the sickle cell and thalassaemia (SCT) antenatal and newborn screening programme.
Information for pregnant women to understand what it means to be a sickle cell carrier.
How to support patients in accessing population screening programmes and obtaining screening results.
Leaflet for expectant fathers explaining antenatal screening for sickle cell and thalassaemia.
Information for parents of babies who carry the sickle cell gene.
This document sets out for the programme specific operating model (PSOM) for quality assurance of the NHS antenatal and newborn (ANNB) screening programmes.
Role and remit of NHS population screening programmes’ Research, Innovation and Development Advisory Committee
Information for parents of babies who carry a gene for unusual haemoglobin.
Training and continuing professional development for people working in the sickle cell and thalassaemia screening programme in England.
Guidance to support the health system to reduce inequalities in screening.
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