Safe and Accurate Prenatal Genetic Testing With NIPT

Our Non-Invasive Prenatal Genetic Test (NIPT) allows expectant parents to screen for common chromosomal abnormalities, including Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13), without any risk to the baby or mother.

Using a maternal blood sample, fetal DNA is analyzed in a certified laboratory to provide highly accurate early screening results.

How It Works:

1. Sample Collection – A simple maternal blood draw, typically from 10 weeks of pregnancy onward.

2. Laboratory Analysis – Accredited labs isolate and analyze fetal DNA for chromosomal abnormalities.

3. Results Delivery – Receive a detailed, confidential report within the turnaround time provided.

Why Choose Our NIPT:

• Non-Invasive & Safe – No risk to mother or baby

• Early Detection – Can be performed from 10 weeks of gestation

• Clinically Validated – Accredited, internationally recognized laboratories

• Confidential & Secure – Private results delivered directly to you

• Worldwide Availability – Sample collection and shipping options for international clients

Who Should Use This Test:

• Expectant mothers seeking early detection of chromosomal conditions

• Healthcare providers and fertility clinics

• Parents seeking peace of mind with accurate prenatal screening

Shipping / Service Note:

• UK clients: Price as displayed.

• International clients: Contact us via email, WhatsApp, or phone for collection, lab processing, and shipping fees.