CE-IVD Oncology Applications by SOPHiA GENETICS™

Supporting fast and reliable precision diagnostics with CE-IVD applications powered by SOPHiA DDM™

Discover our CE-IVD Oncology Solutions

We are here to simplify your transition to the new regulatory environment. You can leverage our CE-in vitro diagnostic (IVD) labeled platform and CE-IVD Oncology Applications while staying compliant with IVDD during this transition period. See in our Frequently Asked Questions section for more answers.​

Get ready for a streamlined workflow –
From sample to data to insight​

Our CE-IVD Oncology Applications provide you with robust, meaningful clinical results and help you to discover the full power of your data for your patients. Leverage the potential of an end-to-end CE-IVD solution in oncology genetic testing and reporting.​

Accurate and reliable testing

Confident detection of actionable variants

Reduced time to patient benefit

EU IVDD compliant solutions and software

Contact us to know more

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Discover our CE-IVD Oncology Applications

SOPHiA DDM™ Dx Homologous Recombination Deficiency (HRD) Solution​

Support accurate detection of HRD status in ovarian cancer patients by leveraging low-pass WGS to measure genomic scarring.​

SOPHiA DDM™ For Solid Tumors

SOPHiA DDM™ Dx RNAtarget Oncology Solution (ROS)​

Expect more from your RNA analyses with reliable partner-agnostic detection of fusions in small lung cancer biopsy samples.​

SOPHiA DDM™ For Solid Tumors

SOPHiA DDM™ Dx Solid Tumor Solution (STS)​

Benefit from advanced molecular profiling of solid tumors, including lung, colorectal, skin and brain, with confident SNV and Indel detection in relevant genes.​

SOPHiA DDM™ For Solid Tumors

SOPHiA DDM™ Dx Myeloid Solution​ (MYS)

Expand the scope of myeloid neoplasms management with advanced analytical performance for the detection of pertinent SNVs, Indels and FLT3-ITDs.

SOPHiA DDM™ For Solid Tumors

SOPHiA DDM™ Dx Hereditary Cancer Solution (HCS)

Confidently assess crucial variants associated with hereditary cancers with tailored analytics that accurately detect key SNVs and Indels.

SOPHiA DDM™ For Solid Tumors

Indels, insertions/deletions. ITDs, internal tandem duplications; SNVs, single nucleotide variants; WGS, whole genome sequencing