PGDx elio tissue complete enables you to confidently advise your oncologists and gain new research advantages with our sample-to-answer CE-IVD kit that includes fully automated bioinformatics and dedicated customer support.
The CE-IVD marked marked tumor profiling kitted solution
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Benefits of the PGDx pan solid tumor CGP test
PGDx elio tissue complete enables you to confidently advise your oncologists and gain new research advantages with our sample-to-answer CE-IVD kit that includes fully automated bioinformatics and dedicated customer support.
Our test, your lab
Offer rapid comprehensive, scalable genomic testing and report on actionable findings with confidence with 5 day* turnaround from isolated nucleic acid to variant report.
Accelerate your path to test launch and reimbursement
CE-marked and FDA-cleared solution allows for verification, not validation. Professional services available with dedicated implementation project management with custom script development enables seamless integration. Go-live in 6 weeks.
Enable new opportunities
Activate new research opportunities and unlock new potential paths to reimbursement.
Gene panel with TMB and MSI
Solid tumor types
FDA-cleared
Days from isolated nucleic acid to variant report*
Weeks to go live
Clinical success rate
*Kitted workflow plus pipeline output. Not inclusive of DNA extraction and downstream processing
This test identifies somatic mutations with high accuracy and sensitivity, providing information on single nucleotide variants (SNVs), insertions/deletions (indels), amplifications, translocations, microsatellite instability (MSI) status and tumor mutation burden (TMB) for use by qualified professionals to guide treatment decisions.
Patent Disclaimer
For In Vitro Diagnostic Use.
Personal Genome Diagnostics Inc. (PGDx) is a subsidiary of Laboratory Corporation of America Holdings, using the brand Labcorp.
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