Hours of toxicology cross-referencing,
answered in seconds.

ToxIQ is an AI-powered clinical toxicology decision-support assistant. It explains detection windows, cutoff concentrations, metabolite ratios, and specimen validity, and is designed to apply current HHS federal-workplace and DOT 49 CFR Part 40 sources when they govern the question.

ToxIQ is built for Medical Review Officers (MROs), healthcare providers, substance use counselors, employers, drug court personnel, and attorneys — anyone who needs fast, evidence-based background on drug and toxicology test results. For each of them it is a reference and preparation tool, not a substitute for the MRO, clinician, or retained expert whose judgment the decision actually rests on.

You can ask an in-scope toxicology question in plain language or upload a supported lab result as a PDF, CSV, or image. ToxIQ returns decision support covering detection windows, screening and confirmation cutoffs, metabolite ratios, possible interferences, specimen-validity findings, and issues that require qualified professional review.

ToxIQ is designed to apply current HHS federal-workplace guidance and the DOT 49 CFR Part 40 framework when relevant, and to distinguish those regulated programs from clinical laboratories that use their own methods and cutoffs. Users should verify the current governing source and reporting laboratory before acting on a result.

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.

ToxIQ covers six specimen types — urine, oral fluid, hair, blood, sweat, and nails — across common toxicology categories including amphetamines, opioids, benzodiazepines, cannabinoids, cocaine metabolites, and more.

No. ToxIQ is clinical decision support designed to augment professional judgment, not replace it. It does not constitute medical advice, an MRO determination, legal advice, or expert testimony. Every regulated specimen result must be adjudicated by a qualified Medical Review Officer who meets the requirements of 49 CFR § 40.121. ToxIQ also does not decide whether MRO review is required in a given case — that is set by the governing program and by federal, state, and local requirements that vary by jurisdiction, so confirm it with your program administrator or legal counsel.

No. ToxIQ is a research and case-preparation tool. An AI system cannot be qualified as an expert witness, and a ToxIQ analysis is not sworn testimony, an affidavit, or admissible expert opinion. An attorney who intends to rely on the interpretation of a drug test in a proceeding must retain a qualified toxicologist or physician to review the result independently and to testify to it.

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.

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.

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.