Specialty laboratory
High-complexity molecular diagnostics. CLIA number is issued on reports and available to credentialing teams. Insert your number here before public launch.
Quality system
CLIA discipline on a manufacturer’s floor.
Patient Test Solutions, Inc is a clinical laboratory, not a demonstration bench. Resulting, quality-control release, and medical direction sit with this laboratory. Reagents used in testing are manufactured by Atila BioSystems, a separate company.
Method, not brochure
Each assay is validated on the instruments used for clinical work. Accuracy, precision, reportable range, and specimen types are locked in the SOP — not inferred from a kit insert alone.
Same building, separate duty
The laboratory is operationally distinct from reagent manufacturing and sales. Resulting, quality-control release, and medical direction sit with Patient Test Solutions, Inc.
Controls
A single platform makes quality control stricter, not looser.
When every kit and every instrument share a vendor, lot-to-lot and instrument-to-instrument comparisons become possible. We treat that as an obligation.
Lot
Incoming reagent qualification before clinical use.
Run
Internal controls on iAMP / AmpFire / qPCR; library quality control and cluster metrics on NGS.
Instrument
Scheduled function checks on PowerGene, iAMP, extraction, and Illumina sequencers.
Call
Two-step review on NGS and selected oncology PCR before release.
Legal & clinical use
How to read this website
Assays may be FDA-cleared kits or laboratory-developed tests performed under CLIA. This site is informational and is not medical advice. Provider ordering is available now; a public path to request or purchase tests may be added later. Replace placeholder CLIA, CAP, and medical-director fields with issued credentials before go-live.
CLIA # — on file
Medical director — on file
CAP — optional, add if enrolled
NPI / PT programs — on file