Tutorial review on validation of liquid chromatography–mass spectrometry methods: Part II
This is the part II of a tutorial review intending to give an overview of the state of the art of
method validation in liquid chromatography mass spectrometry (LC–MS) and discuss …
method validation in liquid chromatography mass spectrometry (LC–MS) and discuss …
Empirical approaches to uncertainty analysis of X-ray computed tomography measurements: A review with examples
H Villarraga-Gómez, JD Thousand, ST Smith - Precision Engineering, 2020 - Elsevier
The substitution method—an empirical approach for uncertainty assessment (adapted from
the ISO 15530-3 guidelines) that is based on a comparison between repeated …
the ISO 15530-3 guidelines) that is based on a comparison between repeated …
Benchmarking observational uncertainties for hydrology: rainfall, river discharge and water quality
This review and commentary sets out the need for authoritative and concise information on
the expected error distributions and magnitudes in observational data. We discuss the …
the expected error distributions and magnitudes in observational data. We discuss the …
Dimensional metrology with X-ray CT: A comparison with CMM measurements on internal features and compliant structures
X-ray computed tomography (CT) is uniquely suited for dimensional measurement of
components having internal geometry, difficult-to-reach part features, and easy-to-deform or …
components having internal geometry, difficult-to-reach part features, and easy-to-deform or …
Methods for the SI-traceable value assignment of the purity of organic compounds (IUPAC Technical Report)
S Westwood, K Lippa, Y Shimuzu, B Lalerle… - Pure and Applied …, 2023 - degruyter.com
The “purity” of an organic compound typically refers, in practice, to an assignment of the
mass fraction content of the primary organic component present in the material. The “purity” …
mass fraction content of the primary organic component present in the material. The “purity” …
The NISTmAb Reference Material 8671 value assignment, homogeneity, and stability
JE Schiel, A Turner, T Mouchahoir, K Yandrofski… - Analytical and …, 2018 - Springer
Abstract The NISTmAb Reference Material (RM) 8671 is intended to be an industry standard
monoclonal antibody for pre-competitive harmonization of best practices and designing next …
monoclonal antibody for pre-competitive harmonization of best practices and designing next …
[HTML][HTML] Bias in laboratory medicine: the dark side of the moon
A Coskun - Annals of Laboratory Medicine, 2024 - synapse.koreamed.org
Physicians increasingly use laboratory-produced information for disease diagnosis, patient
monitoring, treatment planning, and evaluations of treatment effectiveness. Bias is the …
monitoring, treatment planning, and evaluations of treatment effectiveness. Bias is the …
Bias in clinical chemistry
E Theodorsson, B Magnusson, I Leito - Bioanalysis, 2014 - Taylor & Francis
Clinical chemistry uses automated measurement techniques and medical knowledge in the
interest of patients and healthy subjects. Automation has reduced repeatability and day-to …
interest of patients and healthy subjects. Automation has reduced repeatability and day-to …
Validation and verification of measurement methods in clinical chemistry
E Theodorsson - Bioanalysis, 2012 - Taylor & Francis
The present overview of validation and verification procedures in clinical chemistry focuses
on the use of harmonized concepts and nomenclature, fitness-for-purpose evaluations and …
on the use of harmonized concepts and nomenclature, fitness-for-purpose evaluations and …
Permissible limits for uncertainty of measurement in laboratory medicine
R Haeckel, W Wosniok, E Gurr, B Peil - Clinical Chemistry and …, 2015 - degruyter.com
The international standard ISO 15189 requires that medical laboratories estimate the
uncertainty of their quantitative test results obtained from patients' specimens. The standard …
uncertainty of their quantitative test results obtained from patients' specimens. The standard …