Analyte stability in clinical chemistry quality control materials.

Abstract:

:Maximum stability of analytes in chemistry control materials is desired. Stability testing is customarily performed by manufacturers, both prior to distribution of products and during the period following distribution when the products are in the field. Users and evaluators of such materials periodically have reported on experienced stability of various analytes in distributed manufactured products. A wide variety of both testing protocols and definitions of acceptable stability have characterized published reports on the topic. In the present review, we summarize published studies on control material stability in clinical chemistry, review criteria employed to define instability, and present an approach to evaluating stability of analytes involving both statistical and clinical criteria.

journal_name

Crit Rev Clin Lab Sci

authors

Lawson NS,Haven GT,Williams GW

doi

10.3109/10408368209107031

subject

Has Abstract

pub_date

1982-01-01 00:00:00

pages

1-50

issue

1

eissn

1040-8363

issn

1549-781X

journal_volume

17

pub_type

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