Dendi Precision Suite
The precision diagnostics platform that scales with your commercialization strategy.
Your existing workflow runs the assay. Precision Suite is the commercialization platform to bring it to market with ordering, reporting, client services, EHR and billing integrations. All from a system built for clinical compliance.
Platform overview
Integrate existing workflows with clinical tools to deliver results to patients
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.
LAB environment
Precision Suite commercial layer
Keep your diagnostics workflow. Add the commercial layer.
Labs preparing for commercialization often consider two options with major challenges before finding a better path:
Precision Suite connects existing systems in lab diagnostics workflows to make your product accessible to clients by receiving results data from your pipeline, generating custom reports, managing patient data, and integrating with billing and EHR systems to quickly enable commercial operations.
Don't rebuild from scratch. Simply, add the tools that takes your assay to market.
Precision Diagnostics assays
Built to support all clinical disciplines
The commercial infrastructure — ordering, custom reports, EHR delivery, billing management, and data analytics — works for different disease targets. Precision Suite is built to launch precision assays across diagnosis, monitoring, and risk assessment — from single-marker tests to multi-omics panels.
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.
Lab types supported
Built to support labs from startup to go-to-market
Precision Suite is built for labs that haved developed novel assays and are ready for commercial infrastructure to go to market.
Startup Assay Development Labs
Labs with a proprietary assay that need operations solutions prior to commercialization into sustained ordering volume.
Lean infrastructure built for growth, not a stopgap that gets outgrown and requires migration.
Precision medicine spinouts
Labs spun out of academic medical centers or research programs with validated assays and a pathway to LDT commercialization.
Implement commercial ops capabilities without disrupting the R&D environment.
Biotech diagnostic divisions
Biotech companies that have developed a companion diagnostic or standalone molecular assay and need a lab commercialization layer.
Provider ordering infrastructure and billing-ready reporting without a full LIMS rebuild.
Specialty reference labs
Reference labs adding novel precision assays alongside their existing menu, managed separately from established testing workflows.
Support for a new assay's commercial launch without rebuilding their existing production LIS.
Track and manage orders
Commercialization is more than lab results — it runs on communication. Precision Suite lets you tag orders by what's needed next: a clinical review, a customer service follow-up, a QC hold. Add context with comments, route the right issue to the right team, and keep the whole order lifecycle, from science to client services all in one place.
- Contact providers directly from the application.
- Add tags to prompt customer service reviews, QC issues, holds or remediation guidelines.
- Add comments to the tags to communicate and audit your teams to-do list.
- Notification workflows and escalation routing for your ops team.
Turn your assay output into a report providers can act on.
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.
- Multiple custom report templates per assay type
- Variant classification, TMB, MSI, and structured interpretation sections
- Historical results and longitudinal trend data surfaced within the report
- Full lab branding — logo, typography, and layout control
- HL7, FHIR, and custom export for downstream EHR and registry delivery
Connects to your diagnostics software. Routes to your business systems.
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.
- Accepts result input from your existing LIMS and diagnostics pipeline via REST API or HL7
- Bidirectional EHR connectivity via HL7 and FHIR
- Instrument and sequencer connections for direct result ingestion
- Billing system integration with CPT and ICD code mapping
- Reference lab send-out and result routing
- Custom export for CRM, commercial reporting, or any downstream consumer
Your diagnostics environment
Result routing & audit log
A commercial system that meets clinical standards.
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.
- CAP / CLIA-aligned workflow templates and QC documentation
- Per-sample QC with lot traceability and Levey-Jennings charts
- Full audit trail across every order, result, and user action
- SSO integration and role-based permissions across all users
CAP / CLIA workflows
Pre-configured QC and documentation designed to align with CAP checklist requirements for molecular and oncology labs.
QC Traceability
Track your control lots, expiration information, and generate Levey-Jennings charts for full quality control reports.
Enterprise-Grade Security
Data practices, encryption, access controls, and audit logging aligned with SOC 2 Type II requirements.
SSO & access controls
Role-based permissions, SSO integration, and per-user audit logs across all system activity.
One source of truth from order to result.
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.
- Provider and ordering activity dashboards
- TAT analytics with per-assay and per-provider breakdowns
- Historical result trends and QC trending over time
- Issues queue with resolution tracking and escalation history
- Custom export for commercial, ops, and finance reporting
This month · June 2026
Provider activity — top 5 this month
Timeline
From integration to first commercial orders in 6 weeks.
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. Complex integrations or multi-EHR setups typically run 6–10 weeks.
Ready to plan your launch?
Talk to the team about your assay and your timeline.
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
Your assay is ready. Let's commercialize it.
Meet with us to learn about how we can help bring your test to market.
Request a demo