How Should a UDT Panel Be Designed?

For healthcare organizations and professionals (B2B) · Physician-led · Updated 2026-07-12 · CLIA #45D2048957 · CAP #8722734
Molecular fluorescence imaging — Auspicious Laboratory, Houston
The right panel is the smallest one that answers your question. Analyte maximization is a compliance risk, not a service.CLIA #45D2048957 · CAP #8722734 · Same-day results · Walk-ins welcome
Around your patient population and your clinical question — not around the number of billable analytes. A pain practice, an addiction treatment program and an employer have genuinely different needs. What all three share is one non-negotiable: fentanyl must be targeted specifically, because a standard opiate screen will not see it.
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Design principles

PrincipleWhy
Start from the clinical questionPanel scope follows medical necessity, and is documented
Always include fentanyl / norfentanylThe dominant driver of overdose deaths, invisible to opiate screens
Include prescribed medicationsAdherence assessment requires them — medication monitoring
Define reflex rules on clinical criteriaNot "confirm everything, every time"
State coverage explicitlyWhat is covered, and what is not. No implied comprehensiveness

A laboratory that proposes the largest possible panel by default is optimizing its billing, not your clinical decision. Ask any lab to justify each analyte against your population — including us.

Compliance. No payment for referrals, no revenue sharing, no inducements. Testing is performed on the basis of medical necessity and a physician order, at fair market value, consistent with the Anti-Kickback Statute and the Stark Law.
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FAQ

Can we start small and expand?
Yes. That is usually the right approach.
Will you tell us to test more?
No. Frequency is a clinical decision and we will not push volume.
Can reflex confirmation be automated?
Yes, on defined clinical criteria rather than blanket rules.
How do we begin?
Call (713) 266-0808 or use the provider portal.
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References

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