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Every scan performed personally by Professor Pandya — no sonographers, only direct consultant expertise, at every appointment.
At Professor Pandya's clinic, every ultrasound scan is performed directly by him. This is not standard practice — many private clinics use sonographers for routine scans. We believe that having a consultant with 37 years of specialist expertise review every image in real time provides unmatched accuracy, reassurance and peace of mind.
All scans take place at the Harley Street Centre for Women, a dedicated specialist centre providing the highest standard of women's health care in central London.
From 6 Weeks
An early pregnancy scan provides vital reassurance at a time when many women feel anxious. It confirms the pregnancy is developing in the correct location, checks for a heartbeat and provides an accurate dating of the pregnancy.
This scan is ideal for women who have experienced previous miscarriage, IVF, fertility treatment, or who are experiencing symptoms such as bleeding or pain and require reassurance.
11–14 Weeks
The Nuchal Translucency (NT) scan is one of the most important scans in pregnancy. It measures fluid at the back of the baby's neck — a key marker used to assess the likelihood of Down's syndrome (Trisomy 21), Edwards' syndrome and Patau's syndrome.
Combined with a blood test (the combined first trimester screen), the NT scan provides a highly sensitive assessment of chromosomal conditions, helping you make informed decisions about any further testing.
20–22 Weeks
The Detailed Anatomy Scan, also known as the anomaly scan, is a comprehensive examination of your baby's anatomy at the mid-point of pregnancy. Professor Pandya reviews each organ system in detail — including the brain, spine, heart, kidneys, limbs and face.
This scan goes beyond the NHS routine 20-week scan, with greater time, attention and consultant expertise applied to every structure. Where a potential concern is found, Professor Pandya can provide immediate expert interpretation and guidance.
28 Weeks Onwards
As your pregnancy progresses into the third trimester, a Fetal Wellbeing Scan provides reassurance about your baby's growth, movements, position and placental function. This is particularly important for women with risk factors for fetal growth restriction or placental problems.
The scan includes Doppler blood flow assessment to evaluate the blood supply through the umbilical cord and placenta, providing a complete picture of your baby's health in late pregnancy.
From 10 Weeks
PrenatalSafe® 3 is a non-invasive prenatal screening test (NIPT) that analyses fetal DNA from a simple maternal blood sample. It is designed to assess the risk of common chromosomal conditions including Down’s syndrome (Trisomy 21), Edwards’ syndrome (Trisomy 18) and Patau’s syndrome (Trisomy 13) with a high level of accuracy.
This advanced screening test provides early reassurance during pregnancy and may help reduce the need for invasive diagnostic procedures.
From 10 Weeks
PrenatalSafe® Complete Plus is an advanced non-invasive prenatal screening test (NIPT) that analyses fetal DNA from a simple maternal blood sample. It provides comprehensive screening for common chromosomal conditions, sex chromosome abnormalities and selected microdeletion syndromes with a high degree of accuracy.
This detailed prenatal screening test offers early reassurance during pregnancy and supports informed decision-making without the risks associated with invasive procedures.
From 9 Weeks Onwards
The Panorama Test is an advanced non-invasive prenatal screening test (NIPT) that analyses fetal DNA from a simple maternal blood sample. Using highly accurate SNP-based technology, it assesses the risk of common chromosomal conditions and selected genetic abnormalities during pregnancy.
The test provides early reassurance and personalised insights into your baby’s health while reducing the need for invasive diagnostic procedures.
From 9 Weeks
The KNOVA Test is an advanced non-invasive prenatal screening test (NIPT) that analyses fetal DNA from a simple maternal blood sample. It provides highly accurate screening for common chromosomal conditions and selected genetic abnormalities early in pregnancy.
This safe and reliable screening test offers reassurance and supports informed pregnancy care without the risks associated with invasive testing procedures.
