The science

Rigor before rollout.

The launch gate is clinical validation: the right device, sample, laboratory and path for clinician review.

01

Start with the laboratory report

Reference ranges come from the testing laboratory.

BaselineDX will display the ranges and flags supplied by the contracted clinical laboratory. We will not replace a lab flag or a clinician’s judgment with an invented wellness range.

02

Why context matters

A single biomarker rarely tells the whole story.

Related markers, collection timing, medications and health history can change interpretation. Results are information for a clinical conversation, not a diagnosis by themselves.

03

Why longitudinal data helps

Trends can add context to a snapshot.

When a clinician recommends retesting, consistent methods and timing make changes easier to evaluate. The appropriate interval depends on the marker, result and patient—not a fixed membership schedule.

Launch methodology

What must be verified before the first order.

Collection validation

The exact upper-arm device, sample type, volume and number of tubes required for every tier.

Laboratory credentials

CLIA certification, CAP accreditation where claimed, Utah availability and a signed business associate agreement.

Clinical workflow

Assay validation, critical-result escalation, failed-collection handling and secure patient/provider access.

Clinical oversight

Dr. Porter’s clinic will review the pilot workflow. Laboratory interpretation, ordering authority and escalation responsibilities will be documented with the selected vendor before testing begins.