Summary of validation considerations with real‐life examples using both qualitative and semiquantitative flow cytometry assays

Author:

Devitt Katherine A.12,Oldaker Teri3,Shah Kalpesh4,Illingworth Andrea5

Affiliation:

1. Department of Pathology and Laboratory Medicine University of Vermont Medical Center Burlington Vermont USA

2. Larner College of Medicine at the University of Vermont Burlington Vermont USA

3. Oldaker Consulting San Clemente California USA

4. Sunnybrook Health Science Centre Toronto Ontario Canada

5. Dahl‐Chase Diagnostic Services Bangor Maine USA

Abstract

AbstractIn the clinical laboratory, flow cytometry assays are critical to providing diagnostic and prognostic information to the treating clinicians. A validation or verification provides confidence that the assay will yield reliable results that can be trusted to make critical medical decisions. The following performance specifications should be included in a validation for laboratory developed tests as needed: accuracy (or trueness), precision (reproducibility and repeatability), detection capability, selectivity, reference range, and sample and reagent stability. We define these terms and present our approach to validation of several common flow cytometry assays, including examples of a leukemia/lymphoma assay and a paroxysmal nocturnal hemoglobinuria (PNH) assay.

Publisher

Wiley

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

Reference19 articles.

1. Recommendations for the evaluation of specimen stability for flow cytometric testing during drug development

2. Centers for Medicare & Medicaid Services Department of Health and Human Services. (2003).Laboratory requirements: Establishment of verification of performance specifications (codified at 42 CFR §493.1253(b)). Office of the Federal Register.

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