Validation in Chemical MeasurementPaul De Bièvre, Helmut Günzler Springer Science & Business Media, 2005. gada 6. dec. - 168 lappuses The validation of analytical methods is based on the characterisation of a measurement procedure (selectivity, sensitivity, repeatability, reproducibility). This volume collects 31 outstanding papers on the topic, mostly published in the period 2000-2003 in the journal "Accreditation and Quality Assurance." They provide the latest understanding, and possibly the rationale why it is important to integrate the concept of validation into the standard procedures of every analytical laboratory. In addition, this anthology considers the benefits to both: the analytical laboratory and the user of the measurement results. |
No grāmatas satura
1.–5. rezultāts no 36.
. lappuse
... Analytical Chemistry Department . Crtra . Zaragoza , s / n 22071 Huesca , Spain . R. C. Díaz University of Zaragoza , Analytical Chemistry Department . Crtra . Zaragoza , s / n 22071 Huesca , Spain Stephen L. R. Ellison Laboratory of ...
... Analytical Chemistry Department . Crtra . Zaragoza , s / n 22071 Huesca , Spain . R. C. Díaz University of Zaragoza , Analytical Chemistry Department . Crtra . Zaragoza , s / n 22071 Huesca , Spain Stephen L. R. Ellison Laboratory of ...
. lappuse
... Chemist , Queens Road , Teddington , Middlesex , TW11 OLY , UK Eugenija Ramoškienė Institute of Chemistry , Goštauto , 92600 Vilnius , Lithuania C. Ríos University of Zaragoza , Analytical Chemistry Department . Crtra . Zaragoza , s / n ...
... Chemist , Queens Road , Teddington , Middlesex , TW11 OLY , UK Eugenija Ramoškienė Institute of Chemistry , Goštauto , 92600 Vilnius , Lithuania C. Ríos University of Zaragoza , Analytical Chemistry Department . Crtra . Zaragoza , s / n ...
1. lappuse
... analytical method validation an integral part of quality management and accredita- tion in analytical toxicology. There- fore, consensus should be reached in this field on the kind and extent of validation experiments as well as on ...
... analytical method validation an integral part of quality management and accredita- tion in analytical toxicology. There- fore, consensus should be reached in this field on the kind and extent of validation experiments as well as on ...
2. lappuse
... Analytical Methods Validation: Bioavailabil- ity, Bioequivalence and Pharmacokinetic Studies” held in Washington in 1990 (Conference Report) [2]. During this conference, consensus was reached on which param- eters of bioanalytical ...
... Analytical Methods Validation: Bioavailabil- ity, Bioequivalence and Pharmacokinetic Studies” held in Washington in 1990 (Conference Report) [2]. During this conference, consensus was reached on which param- eters of bioanalytical ...
5. lappuse
... Chemistry jour- nal, an experimental design with two replicates per run, two runs per day over 20 days for each ... analysis of blank not applicable for most quantita- tive chromatographic methods, as here the response is usually ...
... Chemistry jour- nal, an experimental design with two replicates per run, two runs per day over 20 days for each ... analysis of blank not applicable for most quantita- tive chromatographic methods, as here the response is usually ...
Saturs
1 | |
10 | |
Clinical reference materials for the validation of | 31 |
Qualification and validation of software and computer | 42 |
Validation of the uncertainty evaluation for | 63 |
Validation criteria for developing ionselective | 73 |
quality assurance | 148 |
Is the estimation of measurement uncertainty a viable | 155 |
Different approaches to legal requirements | 159 |
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acceptance Accred Qual Assur accuracy Anal analysis analyte concentration analytical chemistry analytical measurement analytical method analytical procedure Anklam AOAC AOAC INTERNATIONAL application assessment bias calculated calibration curve capillary cation certified certified reference materials Chem chemical clinical components computer systems corrosion criteria CRMs defined detector determination documentation drug EURACHEM evaluation experimental factors functions Hewlett-Packard HPLC injection installation instrument interlaboratory International laboratory linearity LLOQ matrix measurement uncertainty ment meth method validation Metrology mmol/l obtained operating parameters peak performance pharmaceutical phase precision protocol qualification quality assurance quantitative quinizarin range recovery reference materials relative standard deviation reliability reproducibility requirements ruggedness testing sample scope of accreditation solution solvent red 24 solvent yellow 124 specifications Springer-Verlag standard deviation Table tainty test methods tion trueness type of tests uncer uncertainty associated uncertainty estimation vali vendor verification Waldbronn