Capabilities
Your existing diagnostics workflow runs the assay. Precision Suite helps bring it to market with ordering, reporting, client services, EHR and billing integrations. All from a system built for clinical compliance.
Platform overview
Your LIMS and existing systems handle the proprietary science. Precision Suite adds the commercial layer that connects your results to your market: providers, clinicians, and patients.
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Precision Suite commercial layer
Full audit trail across all integrations · configurable per channel
Precision Diagnostics assays
The commercial infrastructure — ordering, reporting templates, EHR delivery, billing codes, and analytics — works across all indication types. Precision Suite is built to launch any structured assay output.
Oncology
Solid tumors, liquid biopsy, and hereditary cancer — with variant classification, TMB, MSI, and structured panel reporting.
Cardiovascular
Genetic risk panels, biomarker assays, and inherited cardiomyopathy testing.
Neurodegenerative
Early detection and progression biomarkers for Alzheimer's, Parkinson's, and ALS.
Rare disease
Whole-exome, gene panels, and functional genomic assays for rare and ultra-rare conditions.
Who this is for
Precision Suite is built for labs that develop their own tests and need commercial infrastructure to go to market.
Lab type
Labs spun out of academic medical centers or research programs with validated assays and a pathway to LDT commercialization.
Need to build commercial ops from scratch without disrupting the R&D environment already in place.
Lab type
Biotech companies that have developed a companion diagnostic or standalone molecular assay and need a lab commercialization layer.
Need provider ordering infrastructure and billing-ready reporting without a full LIS rebuild.
Lab type
Reference labs adding novel precision assays alongside their existing menu, managed separately from established testing workflows.
Need to support a new assay's commercial launch without rebuilding their existing production LIS.
Novel diagnostic assays face commercial challenges when ordering, tracking, and result delivery add friction for providers. Precision Suite gives your lab the operational infrastructure to support clinical adoption from day one — without rebuilding your diagnostics workflows.
Precision Suite receives structured result data from your diagnostics software and pipeline, then generates the clinical-grade reports your providers need — formatted for your assay, branded for your lab, and delivered through the channels they actually use.
Variant findings
Interpretation
Variant findings
Interpretation
CSF biomarker results
Interpretation
Precision Suite is designed to receive result data from your existing diagnostics environment — whatever systems and pipelines you already use — and route it to the commercial systems your business depends on. You don't rebuild. You connect.
Your diagnostics environment
Result routing & audit · configurable per channel
Your commercial-facing system carries the same compliance burden as your diagnostics operations. Payer relationships, enterprise procurement, and CAP/CLIA accreditation all require documented evidence of security, quality, and operational controls. Precision Suite is built for that environment.
Pre-configured QC and documentation designed to align with CAP checklist requirements for molecular and oncology labs.
Lot traceability, QC trending, and Levey-Jennings charts built into every assay workflow.
Data practices, access controls, and audit logging aligned with SOC 2 Type II requirements.
Role-based permissions, SSO integration, and per-user audit logs across all system activity.
Commercial teams need to know which providers are ordering, where samples are getting stuck, and what's hurting adoption. Lab directors need TAT and QC data. Finance needs billing status. Precision Suite brings it together in a single operational view.
This month · June 2026
Provider activity — top 5 this month
Time to market New
Precision Suite is designed to go live alongside your diagnostics environment without a rebuild. Labs typically reach live ordering within 3–6 weeks of starting implementation.
Week 1–2
Integration scoping & API connection
Connect Precision Suite to your existing LIMS or diagnostics pipeline via REST API or HL7. Map your result data structure to the reporting schema. No code changes required on your side in most cases.
Week 2–4
Report template build & provider portal setup
Build your custom report template — lab branding, interpretation sections, variant tables, or any structured result output. Configure the provider portal, initiate EHR interfaces, and test the ordering workflow end-to-end.
Week 4–6
QC workflow validation & compliance documentation
Validate QC workflows against your CAP/CLIA checklist. Run test orders through the full cycle. Generate compliance documentation for your internal quality system.
Week 6+
Live — first commercial orders
Go live with your first ordering providers. Your diagnostics environment continues unchanged; Precision Suite handles ordering, result delivery, and billing in parallel.
Timeline varies by integration complexity and whether EHR delivery is required at launch. Complex NGS pipeline integrations or multi-EHR setups typically run 6–10 weeks.
Ready to plan your launch?
We scope every implementation around your existing diagnostics environment. Most labs start with a 30-minute technical review before kickoff.
Technical review — walk us through your current LIMS and pipeline setup.
Integration scoping — we confirm the API connection approach and data mapping requirements.
Timeline estimate — you get a specific go-live date, not a range.
Ready when you are
Talk to the team about your assay and your timeline.
Request a demo