Resources

Next generation sequencing indeed created a wide universe of data and opportunities in clinical diagnostics. To help you navigate this universe with confidence, to exploit the full potential of the different applications and to enable a smooth take-off with our varvis^® software, our team summarized some basic knowledge, expert tips and tricks, and latest insights for your convenience. We are here to support your onboarding with all the training you need.

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Watch now our webinar on-demand: "From raw data processing to variant classification: A complete software solution with IVDR certificate"

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The varvis^® Software: The first genomics end-to-end software certified as IVDR Class C device

by Dr. Ben Liesfeld, May 31, 2024

Genetic diagnostic laboratories now have access to the first complete genomics software solution which is certified as a Class C device under IVDR. This will significantly reduce the effort required for legally compliant documentation of in-house tests.

Q&A: The role of the IVDR conformity assessment in genetic diagnostics

by Dr. Ben Liesfeld & Dr. Sonja Strunz,
May 31, 2024

Now that the regulation on in-vitro diagnostic devices (IVDR) explicitly regulates in-house devices, or laboratory-developed tests (LDTs), in the European Union, the selection of properly CE-labeled devices is increasingly important to health institutions like genetic testing laboratories.'

The varvis^® onboarding process

by Dr. Roberta Trunzo, April 16, 2024

Welcome to the varvis^® software! We understand that, as a new customer, navigating through a new software platform can be overwhelming. That’s why we’ve created this comprehensive guide to get an overview of all the steps in the process. Our mission? To facilitate a smooth onboarding to our reliable and high-performance varvis^® software and this step-by-step walk-through will ensure you make the most out of it.

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