SignalPGx

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SignalPGx

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SignalPGx

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Built For Clinical Labs

White-label pharmacogenomic (PGx) reporting for clinical laboratories —
CPIC-based gene–drug guidance, physician-reviewed reports, clear pricing.

White-label pharmacogenomic (PGx) reporting for
clinical laboratories — CPIC-based gene–drug guidance,
physician-reviewed reports, clear pricing.

SignalPGx platform open on a monitor in a clinical lab, showing PGx report medication guidance and gene–drug findings, with a printed pharmacogenomic report on the desk

VALUES • IDEAS • VIEW •VALUES • IDEAS • VIEW •

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THE PGx REPORT

What
You Deliver

Every report pairs a patient’s genotype with CPIC-based
gene–drug guidance: phenotype calls, actionable flags, and
prescribing notes traced to source — under your lab’s brand.

Every report pairs a patient’s genotype with CPIC-based
gene–drug guidance — under your lab’s brand.

DOWNLOAD PGx REPORT

Anyone can reprint a guideline. We reconcile 20+ evidence sources into one answer your clinicians can actually defend.

Anyone can reprint a guideline. We reconcile 20+ evidence sources into one defensible answer.

Most PGx reports lean on one guideline set. We reconcile 20+ curated sources — CPIC, DPWG, FDA labels, PharmGKB, PharmVar, ClinVar — resolve the conflicts, and trace every recommendation to its source.

Most PGx reports lean on one guideline set. We reconcile 20+ curated sources —

CPIC, DPWG, FDA labels, PharmGKB, PharmVar, ClinVar — resolve the conflicts, and trace every recommendation to its source.

Most PGx reports lean on one guideline set.

We reconcile 20+ curated sources — CPIC, DPWG, FDA labels,

PharmGKB, PharmVar, ClinVar — and trace every recommendation to its source.

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HOW IT WORKS

One pipeline that turns a raw genotype

into a signed report

One pipeline that turns a raw genotype into a signed report

Every report follows the same audited path —
from intake to EHR delivery, under your brand.

INTAKE — MINUTES

Any Format Accepted

VCF, CSV, array or LIS feed — normalized on arrival, with no re-work for your team.

SCORING — SECONDS

Evidence Reconciled

20+ curated sources matched to the patient’s phenotype, with every conflict resolved.

REVIEW — SAME DAY

Physician Sign-Out

Your medical director reviews and releases, with a full audit trail on every change.

DELIVERY — INSTANT

Branded & Delivered

PDF under your lab’s brand, plus FHIR, HL7 and CDS Hooks straight into the chart.

INTAKE — MINUTES

Any Format Accepted

VCF, CSV, array or LIS feed — normalized on arrival, with no re-work for your team.

SCORING — SECONDS

Evidence Reconciled

20+ curated sources matched to the patient’s phenotype, with every conflict resolved.

REVIEW — SAME DAY

Physician Sign-Out

Your medical director reviews and releases, with a full audit trail on every change.

DELIVERY — INSTANT

Branded & Delivered

PDF under your lab’s brand, plus FHIR, HL7 and CDS Hooks straight into the chart.

INTAKE — MINUTES

Any Format Accepted

VCF, CSV, array or LIS feed — normalized on arrival, with no re-work for your team.

SCORING — SECONDS

Evidence Reconciled

20+ curated sources matched to the patient’s phenotype, with every conflict resolved.

REVIEW — SAME DAY

Physician Sign-Out

Your medical director reviews and releases, with a full audit trail on every change.

DELIVERY — INSTANT

Branded & Delivered

PDF under your lab’s brand, plus FHIR, HL7 and CDS Hooks straight into the chart.

INTAKE — MINUTES

Any Format Accepted

VCF, CSV, array or LIS feed — normalized on arrival, with no re-work for your team.

SCORING — SECONDS

Evidence Reconciled

20+ curated sources matched to the patient’s phenotype, with every conflict resolved.

REVIEW — SAME DAY

Physician Sign-Out

Your medical director reviews and releases, with a full audit trail on every change.

DELIVERY — INSTANT

Branded & Delivered

PDF under your lab’s brand, plus FHIR, HL7 and CDS Hooks straight into the chart.

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IN PRACTICE

Pharmacogenomic reporting that’s intelligent, evidence-backed, and built for real clinical impact.
Real problems. Clear execution. You’ll have the space to think — and the freedom to build.

SignalPGx turns complex genetic data into clear, evidence-backed medication guidance. Living reports from 20+ sources — every step, from generation to clinical review to patient delivery, built for accuracy and better outcomes.

Tarek Younis
Founder & CEO

SignalPGx PGx Report Summary open in a molecular lab, showing CYP2D6, CYP2C19 and DPYD gene panels ready for clinical review

IN THE LAB / PGx REPORT SUMMARY

Genotype quality, gene panels and actionable results — checked before release.

IN THE LAB / PGx REPORT SUMMARY

Genotype quality and gene panels — checked before release.

IN THE LAB / PGx REPORT SUMMARY

Genotype quality and gene panels — checked before release.

Printed SignalPGx pharmacogenomics report showing gene summary, phenotype interpretation and actionable risk badges

IN HAND / THE SIGNED REPORT

Physician-reviewed PGx guidance, printed under your lab’s brand.

IN HAND / THE SIGNED REPORT

Physician-reviewed PGx guidance, printed under your lab’s brand.

IN HAND / THE SIGNED REPORT

Physician-reviewed PGx guidance

SignalPGx Clinical Intelligence dashboard showing medication risk for clopidogrel, sertraline and codeine, beside the patient PGx Passport

AT THE DESK / CLINICAL INTELLIGENCE

Medication risk and the patient’s PGx Passport, live in one view.

AT THE DESK / CLINICAL INTELLIGENCE

Medication risk and the patient’s PGx Passport, live in one view.

Play

Inside SignalPGx

1:42 min overview

Play

Inside SignalPGx

1:42 min overview

ACTIVITY

Operational
Decisions

Automated decisions

across deployed AI systems

+15%

jun.

+35%

jul.

+53%

aug.

Predictability
over heroics.

Systems beat intuition — every time.

Medication Intelligence Graph

Living Reanalysis & Alerts

PGx Revenue Defense Engine

HelioDesk

Platforms

HelioDesk

Platforms

HelioDesk

Platforms

40+ teams

Be the next success story

Benchmark

System
Recovery

Faster operational recovery

To launch branded

PGx REPORTING

after AI decision automation

See the report your lab
would put its name on

See the report your lab would put its name on

A full sample report — physician-reviewed, with every recommendation cited.

A full sample report — physician-reviewed,
with every recommendation cited.

DOWNLOAD PGx REPORT

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PRICING

Pricing Plans

Per-report pricing that scales with volume, not headcount —
no build cost, no bioinformatics hire, no guideline maintenance.

Per-report pricing that scales with volume, not headcount — no build cost, no bioinformatics hire, no guideline maintenance.

Every plan includes physician-reviewed reports, 20+ curated evidence sources, and delivery into the EHR.

INCLUDED IN EVERY PLAN

Pilot through Enterprise

TALK TO SALES

Every plan includes physician-reviewed reports, 20+ curated evidence sources, and delivery into the EHR.

INCLUDED IN EVERY PLAN

Pilot through Enterprise

TALK TO SALES

SignalPGx brought structure and clarity to how we approached AI — and helped us ship systems that actually work in production.

INCLUDED IN EVERY PLAN

Pilot through Enterprise

TALK TO SALES

Pilot

Who it’s for:

For labs validating PGx before committing to a full reporting line. Run real cases end to end under your own brand.

Includes

Core pharmacogenomic gene panel

Branded, physician-reviewed PDF reports

VCF, CSV and array intake

Email support

White-label pharmacogenomic (PGx) reporting forclinical laboratories — CPIC-based gene–drug guidance,physician-reviewed reports, clear pricing.

PGx Reporting (Rx)

PGx Reporting (Rx)

What You Deliver

WhatYou Deliver

Every report pairs a patient’s genotype with CPIC-based gene–drug guidance — under your lab’s brand.

One pipeline that turns a raw genotype

into a signed report

One pipeline that turns a raw genotype into a signed report

Genotype quality and gene panels — checked before release.

Genotype quality and gene panels — checked before release.

Physician-reviewed PGx guidance, printed under your lab’s brand.

See the report your labwould put its name on

See the report your lab would put its name on

A full sample report — physician-reviewed, with every recommendation cited.

Pricing Plans

Pricing Plans

Pricing Plans

Per-report pricing that scales with volume, not headcount — no build cost, no bioinformatics hire, no guideline maintenance.

A clear path —from kickoff to first signed report

We keep implementation structured and predictable — scoped around your panel, your brand, and your existing lab systems.

White-label pharmacogenomic (PGx) reporting for
clinical laboratories — CPIC-based gene–drug guidance,
physician-reviewed reports, clear pricing.

PGx
Reporting (Rx)

What
You Deliver

What
You Deliver

Every report pairs a patient’s genotype with CPIC-based
gene–drug guidance — under your lab’s brand.

See the report your lab
would put its name on

A full sample report — physician-reviewed,
with every recommendation cited.

A clear path —
from kickoff to first signed report