System Performance Monitoring in Clinical Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)

Author:

Haymond Shannon

Publisher

Springer US

Reference13 articles.

1. CLSI (ed) (2007) Mass Spectrometry in the clinical laboratory: general principles and guidance, 1st edn. CLSI C50. Clinical and Laboratory Standards Institute, Wayne

2. CLSI (ed) (2014) Liquid chromatography-mass spectrometry methods, 1st edn. CLSI guideline C62-A. Clinical and Laboratory Standards Institute, Wayne

3. European Medicines Agency (2011) Guideline on bioanalytical method validation. Committee for Medicinal Products for Human Use (EMEA/CHMP/EWP/192217/2009)

4. US Food and Drug Administration. Bioanalytical method validation guidance for industry [Internet] 2018. Available from: https://www.fda.gov/files/drugs/published/Bioanalytical-Method-Validation-Guidance-for-Industry.pdf

5. Hayden J, Bachmann L. Questioning quality assurance in clinical mass spectrometry. Clinical Laboratory News [Internet] 2019 [cited 2022 Jan 10]; Available from: https://www.aacc.org/cln/articles/2019/julyaug/questioning-quality-assurance-in-clinical-mass-spectrometry

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