BioneXt Lab is by your side A laboratory that adapts to your needs and lifestyle

The partnerships we have established, particularly with the CHEM and Picken Doheem , allow us to work anywhere in Luxembourg, and to offer you a top local service guaranteeing optimal medical care.

At BioneXt Lab, your health, comfort and quality of life are all equally important to us. In addition to our sampling centres, we offer a home and workplace sample collection service, calling upon a network of nursing and home care specialists.

Download here the list of partner centers

"MyLAB" allows you to access your test results easily and intuitively at any time from your computer, tablet or smartphone. You can also find the nearest sample collection centres and make an appointment for a blood test at a location of your choice with Picken Doheem, find a doctor by speciality or a health centre and make an appointment with Doctena.

Discover all the features of myLAB on www.bionext.lu/santemobile and download the application on

Are you anxious about taking a blood test?

What you may not know is that this anxiety can have a negative impact on your blood workflow.

There is now a simple and effective way to manage your anxiety.

Our medical solution for self-management of anxiety combines validated therapeutic approaches and Virtual Reality. This technique, which is increasingly used in hospitals, reduces the level of anxiety by up to 82%.

Trisomy is a genetic anomaly that is characterized by the presence of an extra chromosome in the cells of a fetus. The trisomy most frequently encountered in humans is trisomy 21, followed by trisomy’s 18 and 13.
The purpose of the NIPT test is to analyze fetal DNA circulating in the maternal blood by means of high throughput sequencing of DNA via NGS (Next Generation Sequencing) technology coupled with a powerful bioinformatics analysis. This method allows a detection rate of trisomy’s higher than 99% without risk for the fetus.

Fast, reliable and safe, the NIPT can detect trisomy’s 13, 18 and 21 with a simple sample of maternal blood and avoids the risk of miscarriage associated with invasive sampling.