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.
Your LIMS and existing systems handle the proprietary science. Precision Suite adds the commercial layer that connects your results to your market: providers and patients.
Novel diagnotics assays face commercial challenges when ordering, tracking, and result delivery processes add friction for providers. Precision Suite gives your lab the operational infrastructure to support clinical adoption from day one — without rebuilding your diagnostics workflows.
Configure and apply custom tags — issue tags, workflow tags, and more — directly to any order. Filter by tag to maintain a focused working queue for every step you own, so nothing slips through the cracks.
Flag orders for clinical supervisor review, route customer service follow-ups, or mark any action item that needs attention. Resolve tags right inside your work queue — and when you do, add new tags on the fly to hand work off to the right person, sending it straight into their queue.
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.
Two pathogenic variants identified in KRAS and TP53. KRAS G12D is associated with reduced response to anti-EGFR therapy. TMB: 8.4 mut/Mb (intermediate). MSI status: MSS. Clinical correlation recommended.
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 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.
Following the vacating of the FDA LDT rule in 2025, CAP/CLIA accreditation and internal quality systems remain the primary compliance framework for clinical assay labs.
Review security documentationCommercial 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.