Quick,
accurate results

Results returned within an average of
3 business days

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Excellent
detection rate

>99% detection rate for trisomy 21
in published studies

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Low
false-positive rate

Only 0.06% for trisomy 21

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High
success rate

Only 1.4% of samples cannot be analyzed on the first attempt;
only 0.6% after a second attempt.

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Highly qualified medical team
for diagnosis and advice

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The Harmony® Test


The Harmony® Test can reliably detect the risk of the chromosomal disorders trisomy 21, trisomy 18, trisomy 13 as well as X- and Y-chromosomal disorders and DiGeorge syndrome. All aspects of the Harmony® Test are carried out according to european standards of quality and data protection.

Expert opinions on non-invasive prenatal screening test (NIPT)

Performing Harmony® Test

Advantages of the Harmony® Test

  • Excellent detection rate for trisomy 21, 18 and 13


  • Very low false-positive rate


  • Fast turnaround time


  • Excellent clinical validation in studies with more than 148.000 patients


  • Affordable price


  • Feasibility under heparin treatment



Latest News

DAkkS Accreditation DIN EN ISO 15189: 2014

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Our laboratory has been accredited since September 2019 by the DAkkS  according to DIN EN ISO 15189: 2014. The accreditation applies to the scope of accreditation listed in the attachment [D-ML-21205-01-00]. This accreditation certifies medical laboratories a very high standard of quality and competence.

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Harmony Test laboratory analysis requires only 3 working days

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For pregnant women and their families, waiting for the results of a prenatal test is often a huge mental burden. We are pleased to inform you that Cenata has reduced the analysis time for the Harmony® Test by 25% – to just three working days in average. This means that the results of the Harmony® […]

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Procedure of the Harmony® Test


Genetic counseling

Patient requests the Harmony® Test and gets a genetic counseling by obstetrician or human geneticist


Blood sample

Blood sample is taken and the order form is filled out by physician and patient


Shipping

Blood sample and order form are sent


Test performance

Test is carried out, data is analyzed and the findings are compiled


Receipt of report

Physician reports the findings to the patient including genetic counseling