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Ninalia NIPT The prenatal trisomy screening test based on maternal blood sample

Detection rate
of Ninalia NIPT test
Single blood sample
Available from week 10
of pregnancy
Results available
within 5 working days
Can minimize unnecessary invasive sampling by 95%


Non-Invasive Prenatal screening Test for trisomies 13, 18 and 21

Non-invasive prenatal screening is an innovative genetic test designed for pregnant women with a risk of foetal trisomies 13, 18 or 21.

The test is based on the presence of foetal DNA in the maternal blood, combined with the development of a technology (Next Generation Sequencing) capable of counting all genetic material sequences in a maternal blood sample, making it possible to determine whether a trisomy is present in the foetus.

Rapid, reliable and safe, NIPT enables detection of trisomies 13, 18 and 21 while limiting reliance on invasive sampling (amniocentesis or puncture of chorionic villi).

Eurofins Biomnis in figures

As a French laboratory and European leader in specialised medical pathology testing, Eurofins Biomnis has been an expert in the new generation of DNA sequencing techniques for many years and has acquired extensive know-how in the areas of prenatal genetics and biology.

Experts in their fields, the qualified prenatal diagnostics biologists responsible for Ninalia NIPT at Eurofins Biomnis support prescribers, Laboratories and their patients in the implementation of this innovative genetic test.

century of expertise in specialised biology
32 000
medical biology tests every day
2 000
Karyotypes performed
in 2016
14 000
Ninalia tests performed
since october 2014
200 000
Maternal serum markers tests performed
in 2016

Find your nearest testing centre As Ninalia NIPT requires a specific sample tube, don’t forget to make an appointment in advance with your local laboratory for specimen collection.

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