Hours of toxicology cross-referencing,
answered in seconds.
ToxIQ gives MROs, clinicians, counselors, and legal professionals instant, evidence-based interpretation of drug test results — detection windows, cutoffs, metabolite ratios, and specimen validity, all grounded in SAMHSA and DOT guidance.
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See it in action
Ask in plain language, get an evidence-based answer
Type a question or upload a lab result. ToxIQ walks through cutoffs, detection windows, metabolite ratios, and next steps — the way an experienced MRO would.
Who it's for
Built for the professionals who need it most
Healthcare Providers
Understand patient results, medication interactions, and detection window nuances for clinical decisions.
Medical Review Officers
Rapid MRO reference for false positives, chiral analysis, SVT criteria, and DOT 49 CFR Part 40 guidance.
Counselors
Interpret results for treatment clients, explain detection windows, and distinguish use from exposure.
Employers
Understand workplace results, dilute specimens, and when to consult an MRO before taking action.
Judges & Drug Court
Clear, evidence-based explanations for informed rulings in drug court and probation matters.
Attorneys
Challenge or support results with expert-level toxicology context, cutoffs, and error sources.
Features
Everything you need in one place
AI chat with expert toxicology knowledge
Ask any question about detection windows, cutoffs, metabolite ratios, or SVT criteria and get an evidence-based answer instantly.
Lab result interpretation
Upload a PDF, CSV, or image of any lab result and get a full clinical interpretation with red flags and recommendations.
Patient result comparison
Upload two results from the same patient to track changes over time with a side-by-side trend analysis.
PDF report export
Export any conversation as a formatted clinical PDF report with your session details and full interpretation.
Persistent session history
Every conversation is saved and searchable. Resume any past session and continue exactly where you left off.
HIPAA-ready with BAA available
Built for clinical environments with encryption, access controls, and Business Associate Agreements for covered entities.
How it works
Built to be accurate, transparent, and accountable
ToxIQ is a decision-support tool designed to augment professional judgment, never replace it.
Grounded in federal standards
Responses are grounded in SAMHSA workplace testing guidelines and DOT 49 CFR Part 40 framework — the same standards qualified MROs work within.
Human-in-the-loop by design
ToxIQ provides decision support, not determinations. Every regulated result is meant to be adjudicated by a qualified Medical Review Officer. The tool informs your judgment; it never substitutes for it.
Secure and compliant
Patient data is encrypted in transit and at rest, protected by role-based access controls and audit logging. Business Associate Agreements are available for covered entities before any PHI is uploaded.
Randomized testing & compliance
Run a defensible randomized drug testing program
The built-in Randomizer handles the operational side of testing for drug courts, treatment centers, and probation caseloads — fair random selection, patient check-in tracking, automated SMS reminders, and audit-ready compliance reports, all in one place.
Fair random selection
Draw patients for testing on a weekly or monthly schedule with a documented, unbiased selection process.
Check-in tracking
See who was selected, who checked in, and who missed — updated live as patients respond.
Automated SMS reminders
Patients get a text with their check-in code so fewer selections are missed. Consent-based and opt-out ready.
Compliance reports
Export audit-ready reports per caseload for case managers, POs, and the court.
Pricing
Plans built around your practice
Every practice is different, so we price ToxIQ to fit yours. Call for pricing and we'll match you to the right plan — from solo practitioners to full clinics and organizations.
Basic
Everything one practitioner needs
Professional
More volume, plus result comparison
Unlimited
Full access, org codes & BAA
Clinic & Organization Plans
Get your entire clinic on ToxIQ
Individual plans are great for solo practitioners. If you're a clinic, lab, treatment center, or hospital department, we'll set you up with a custom org plan — shared access for your whole team, one bill, one BAA, and a dedicated account manager.
Custom volume pricing
Priced for your team
We'll respond within 1 business day
Unlimited seats
Everyone on your team gets full access under one org account
Org access codes
Share a single code or QR link to onboard your whole team instantly
BAA included
We'll execute a Business Associate Agreement before you upload any patient data
Dedicated support
A real person to help you onboard, train your team, and answer questions
FAQ
Frequently asked questions
What is ToxIQ?
ToxIQ is an AI-powered clinical toxicology assistant that interprets drug test results in seconds. It explains detection windows, cutoff concentrations, metabolite ratios, and specimen validity, with every answer grounded in SAMHSA workplace testing guidelines and the DOT 49 CFR Part 40 framework.
Who uses ToxIQ?
ToxIQ is built for Medical Review Officers (MROs), healthcare providers, substance use counselors, employers, drug court judges, and attorneys — anyone who needs fast, evidence-based interpretation of drug and toxicology test results.
How does ToxIQ interpret a drug test result?
You can ask a question in plain language or upload a lab result as a PDF, CSV, or image. ToxIQ returns a full interpretation that covers detection windows, screening and confirmation cutoffs, metabolite ratios, possible false positives, and specimen validity red flags — with recommendations you can act on.
Is ToxIQ grounded in SAMHSA and DOT guidelines?
Yes. ToxIQ's responses are grounded in SAMHSA workplace drug testing guidelines and the DOT 49 CFR Part 40 regulatory framework — the same standards qualified Medical Review Officers work within.
Can ToxIQ tell the difference between drug use and passive exposure?
ToxIQ helps professionals distinguish likely use from incidental exposure by explaining cutoff concentrations, metabolite ratios, and detection-window context. Final determinations on regulated specimens must still be made by a qualified Medical Review Officer.
Which specimen types and drug classes does ToxIQ cover?
ToxIQ covers six specimen types — urine, oral fluid, hair, blood, sweat, and nails — across more than 50 drug classes, including amphetamines, opioids, benzodiazepines, cannabinoids, cocaine metabolites, and more.
Does ToxIQ replace a Medical Review Officer?
No. ToxIQ is clinical decision support designed to augment professional judgment, not replace it. It does not constitute medical advice, an MRO determination, or a legal opinion. Every regulated specimen result must be adjudicated by a qualified Medical Review Officer licensed under DOT 49 CFR Part 40.
Does ToxIQ help run randomized drug testing programs?
Yes. ToxIQ includes a Randomizer built for drug courts, treatment centers, and probation caseloads. It performs fair, documented random selection of patients on a weekly or monthly schedule, tracks who checked in, sends automated SMS check-in reminders, and exports audit-ready compliance reports for case managers, probation officers, and the court.
Is ToxIQ HIPAA compliant?
ToxIQ is built for clinical environments with encryption in transit and at rest, role-based access controls, and audit logging. A Business Associate Agreement (BAA) is available for covered entities before any protected health information is uploaded.
How much does ToxIQ cost?
ToxIQ offers individual and organization plans priced to fit your practice. Call for pricing or request a demo and our team will match you to the right plan — from solo practitioners to full clinics, labs, and treatment centers.
Still have questions? Email our team or request a demo above.