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 43.
. lappuse
... Experimental and Clinical Toxicology , Institute of Experimental and Clinical Pharmacology and Toxicology , University of Saarland , 66421 Homburg , Germany S. Othake Quality Assurance Department , Sandoz Pharmaceuticals Ltd. , No. 1 ...
... Experimental and Clinical Toxicology , Institute of Experimental and Clinical Pharmacology and Toxicology , University of Saarland , 66421 Homburg , Germany S. Othake Quality Assurance Department , Sandoz Pharmaceuticals Ltd. , No. 1 ...
1. lappuse
... Experimental and Clinical Pharmacology and Toxicology, University of Saarland, 66421 Homburg, Germany e-mail: frank ... experiments as well as on acceptance criteria for validation pa- rameters. In this review, the most im- portant ...
... Experimental and Clinical Pharmacology and Toxicology, University of Saarland, 66421 Homburg, Germany e-mail: frank ... experiments as well as on acceptance criteria for validation pa- rameters. In this review, the most im- portant ...
2. lappuse
... experiments on the established ac- ceptance criteria for accuracy and precision [3]. Based on their results they questioned the suitability of these criteria for practical application. From 1995 to 1997, ap- plication issues like ...
... experiments on the established ac- ceptance criteria for accuracy and precision [3]. Based on their results they questioned the suitability of these criteria for practical application. From 1995 to 1997, ap- plication issues like ...
3. lappuse
... experiments for the first ap- proach can be performed during a pre - validation phase ( no need for quantification ) , those for the second ap- proach are usually performed together with the precision and accuracy experiments during the ...
... experiments for the first ap- proach can be performed during a pre - validation phase ( no need for quantification ) , those for the second ap- proach are usually performed together with the precision and accuracy experiments during the ...
4. lappuse
... experimental design proposed by Wieling et al. four concentration levels (LLOQ, low, medium, high) were studied [6, 12]. Causon also suggested to esti- mate precision at four concentration levels [8]. Several authors have specified ...
... experimental design proposed by Wieling et al. four concentration levels (LLOQ, low, medium, high) were studied [6, 12]. Causon also suggested to esti- mate precision at four concentration levels [8]. Several authors have specified ...
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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Bieži izmantoti vārdi un frāzes
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