Managing the Quality Control of multiple instruments
Author:
Affiliation:
1. Royal College of Pathologists of Australasia Quality Assurance Programs , NSW , Sydney , Australia
2. Biogroup Laboratories , Lyon , France
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://www.degruyter.com/document/doi/10.1515/cclm-2023-0592/pdf
Reference11 articles.
1. Åsberg, A, Solem, KB, Mikkelsen, G. Allowable systematic difference between two instruments measuring the same analyte. Scand J Clin Lab Invest 2014;74:588–90. https://doi.org/10.3109/00365513.2014.921836.
2. Nam, Y, Lee, JH, Kim, SM, Jun, SH, Song, SH, Lee, K, et al.. Periodic comparability verification and within-laboratory harmonization of clinical chemistry laboratory results at a large healthcare center with multiple instruments. Ann Lab Med 2021;42:150–9. https://doi.org/10.3343/alm.2022.42.2.150.
3. Lippi, G, Da Rin, G. Advantages and limitations of total laboratory automation: a personal overview. Clin Chem Lab Med 2019;57:802–11. https://doi.org/10.1515/cclm-2018-1323.
4. Seaberg, RS, Stallone, RO, Statland, BE. The role of total laboratory automation in a consolidated laboratory network. Clin Chem 2000;46:751–6. https://doi.org/10.1093/clinchem/46.5.751.
5. Yago, M, Pla, C. Reference-mean-centered statistical quality control. Clin Chem Lab Med 2020;58:1517–23. https://doi.org/10.1515/cclm-2019-1034.
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