Non-invasive prenatal testing that detects common chromosomal conditions with 99.9% accuracy
Know Your Baby’s
Genetic Health
With A Simple, Safe Test
Non-invasive prenatal testing that detects common chromosomal conditions with 99.9% accuracy
Think of NIPT as a window into your baby’s health that an ultrasound can’t see. It’s a simple blood test that finds tiny fragments of your baby’s DNA in your own bloodstream. We use it to check for chromosomal conditions like Down syndrome early in your pregnancy-with zero risk to the baby and no invasive needles.
Essential screening for early peace of mind
Best for first-time parents and low-risk pregnancies
Maximum clarity. Maximum confidence.
Most popular choice for complete peace of mind
Transparent pricing with no hidden charges. Competitive all-in pricing for at-home NIPT - contact us for the exact package for your pregnancy.
Yes. NIPT is a routine blood test from the mother’s arm. There is no risk to the pregnancy.
NIPT is typically available from 10 weeks of pregnancy. Book early to receive results when they help planning.
NIPT screens for common chromosomal conditions such as trisomy 21 (Down syndrome), trisomy 18, and trisomy 13, and selected chromosome abnormalities. It does not replace diagnostic tests.
NIPT is a screening test. A positive result should be followed by confirmatory diagnostic testing and genetic counselling.
NIPT offers very high sensitivity and specificity for the conditions it screens. Our clinical lab standards ensure reliable screening and fast reporting.
Results are yours to share with your healthcare provider. If you have questions about coverage, our team will help with documentation.
Men Wellness Full Body
Healthy Kid Package
