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Non-Invasive Prenatal Testing (NIPT)
Safe. Early. Accurate. Peace of Mind for Expecting Parents
What is Non-Invasive Prenatal Testing?
Non-Invasive Prenatal Testing (NIPT) is a simple blood test performed on pregnant women to screen for certain genetic conditions in a developing baby. It is called “non-invasive” because no needles or procedures are done on the baby, making it safe for both mother and child.
NIPT can detect conditions like:
Down syndrome (Trisomy 21)
Trisomy 18 & 13
Sex chromosome abnormalities
Some microdeletions (depending on test type)
Who Should Consider NIPT?
Expecting mothers looking for early reassurance
Families with a history of genetic conditions
Healthcare providers seeking safe, accurate screening options
Anyone wanting peace of mind during pregnancy
Why Choose NIPT?
✔ Safe & Non-Invasive – Only a maternal blood draw is required
✔ Early Detection – Can be performed as early as 9–10 weeks of pregnancy
✔ Accurate Screening – High sensitivity for common chromosomal conditions
✔ Confidential & Private – Results shared securely with parents
✔ Quick & Convenient – Mobile or in-office blood collection
How the Process Works:
Schedule a test – Choose a convenient appointment with our mobile or office collection service
Blood sample collection – Simple blood draw from the mother
Laboratory analysis – Accredited lab tests fetal DNA in maternal blood
Results delivered – Clear, easy-to-read report sent confidentially to parents and/or healthcare provider
Important Note ⚠️
NIPT is a screening test, not a diagnostic test. Positive or high-risk results should be followed by confirmatory diagnostic testing, as recommended by your healthcare provider.