Is your assay stable? Using process stability and capability to evaluate assay performance-Reference-Cited by-同舟云学术

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Is your assay stable? Using process stability and capability to evaluate assay performance

Published:2019-03 Issue: Volume:490 Page:28-33
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Schmidt Robert L.,Pearson Lauren N.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference22 articles.

1. Understanding Variation: The Key to Managing Chaos;Wheeler,2000

2. Making control charts more effective by time series analysis: three illustrative applications;Roberts;Commun. Stat. Theor. Meth.,1996

3. Introduction to Statistical Quality Control;Montgomery,2009

4. Understanding Statistical Process Control;Wheeler,2010

5. Statistical Process Control;Oakland,2007

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impact of assay stability on the false negative and false positive rates in quality control;Clinica Chimica Acta;2023-02

2. Risk Analysis for Quality Control Part 2: Theoretical Foundations for Risk Analysis;The Journal of Applied Laboratory Medicine;2023-01-04

3. Optimizing Equity: Working towards Fair Machine Learning Algorithms in Laboratory Medicine;The Journal of Applied Laboratory Medicine;2023-01-04

4. Estimating the cost of quality of errors in the analytical phase;Clinica Chimica Acta;2019-08

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