Qnomx Report
Patient-specific reports that win more referrals and free your senior team
Qnomx Report drafts the full clinical report from each interpretation, tailored to your lab's requirements and local clinical context and language, so pathologists review and approve rather than write from scratch. Customize outputs effortlessly on the fly with agentic chat, so you get the exact final output you need with no copy-paste or manual reconciliation. Faster turnaround, consistent quality across reports, and outputs that hold up under audit.
See Qnomx Report on a real caseDemo report - inquire about customization options for your lab
End-to-end reporting, not point fixes
Augmenting interpretation results with local context like clinical trials and drug approvals, translation, and formatting to your standards is manual work that blocks your reporting pipeline. Qnomx Report covers that whole stage in one step, turning a reviewed interpretation into a clinician-ready report tailored to each patient.
Qnomx Report works on its own with interpretations from your existing workflow, so you can integrate today without changing providers. Paired with Qnomx Insight, which drafts the variant annotations Qnomx Report builds on, you get the most advanced and efficient tertiary workflow on the market. Each product stands alone, and the efficiency gains are largest when you run both.
What Qnomx Report does
Generates clear case-level clinical narratives
Applies your lab's configurable content standards and layout
Supports multilingual output, clinical trial references, and local conventions
Agentic chat enables you to edit outputs or provide custom instructions live, so you get the exact final output you need with no copy-paste or manual rework
Enables structured review and sign-off workflows
Reports stay fully editable. Qualified experts approve before anything is released.
Why labs choose Qnomx Report
Patient-specific from the first draft
Incumbents return generic information about the variant and analysts must manually fill in gaps and remove irrelevant data. Molecular pathologists waste time deleting pages of pembrolizumab indications to get to the one relevant for your patient.
Qnomx Report integrates that context from the start, so the draft your analyst opens is already about this patient, not a generic tertiary output to rework. Stronger, more clinically-relevant reports that delight customers become something your lab competes on.
One standard across every site
Established tools leave formatting and methodology to each analyst, so output drifts between sites and shifts.
Qnomx Report applies one format and methodology everywhere you operate, so quality does not depend on who is on shift or which site ran the case.
Defensible under audit
Incumbents deliver generic statements, and constructing defensible results is a manual process left to individual scientists.
The cited evidence chain from interpretation carries through into the report, so every statement is traceable. When questions come up in audit, accreditation, or peer review, the trail is already there.
What it means for your lab
Faster turnaround, more referrals. Qnomx Report's automated workflows keep pace with rising volumes and panel sizes.
Senior time goes to difficult, complex cases instead of grunt work.
Defensible reports under audit and accreditation, so sign-off is confident and referring physicians trust what they receive.
Consistent quality across reviewers and sites, with smoother onboarding for new staff.
Inquire today, deploy tomorrow
Qnomx Report drafts from your existing interpretations with no LIMS integration, and deploys in as little as 24 hours. Patient data is processed under strict security and privacy standards, with EU and Swiss data residency. No data goes through Silicon Valley models or servers.
Book a demo