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 23.
. lappuse
... the Japanese pharmaceutical industry .... 56 Method validation of modern analytical techniques ... 134 Validation of the uncertainty evaluation for the determination of metals in solid samples by atomic spectrometry ...
... the Japanese pharmaceutical industry .... 56 Method validation of modern analytical techniques ... 134 Validation of the uncertainty evaluation for the determination of metals in solid samples by atomic spectrometry ...
. lappuse
... Pharmaceuticals Ltd. , No. 1 Takeno , Kawagoe City , Saitama , Japan Reinhard Kreßner Federal Environmental Agency , P. O. Box 33 00 22 , 14191 Berlin , Germany Stephan Küppers Schering AG , In - Process - Control , Müllerstrasse 170 ...
... Pharmaceuticals Ltd. , No. 1 Takeno , Kawagoe City , Saitama , Japan Reinhard Kreßner Federal Environmental Agency , P. O. Box 33 00 22 , 14191 Berlin , Germany Stephan Küppers Schering AG , In - Process - Control , Müllerstrasse 170 ...
. lappuse
... Pharmaceuticals Ltd. , No. 1 Takeno , Kawagoe City , Saitama , Japan Frank T. Peters Department of Experimental and Clinical Toxicology , Institute of Experimental and Clinical Pharmacology and Toxicology , University of Saarland ...
... Pharmaceuticals Ltd. , No. 1 Takeno , Kawagoe City , Saitama , Japan Frank T. Peters Department of Experimental and Clinical Toxicology , Institute of Experimental and Clinical Pharmacology and Toxicology , University of Saarland ...
1. lappuse
... pharmaceuticals. This is re- flected by the number of publications on this topic pub- lished in the last decade, of which the most important are discussed here. Important (1991 to present) publications on validation A review on ...
... pharmaceuticals. This is re- flected by the number of publications on this topic pub- lished in the last decade, of which the most important are discussed here. Important (1991 to present) publications on validation A review on ...
2. lappuse
... Pharmaceuticals for Human Use (ICH) and approved by the regulatory agencies of the European Union, the United States of America and Japan. The first, approved in 1994, concentrated on the theoretical background and definitions [13], the ...
... Pharmaceuticals for Human Use (ICH) and approved by the regulatory agencies of the European Union, the United States of America and Japan. The first, approved in 1994, concentrated on the theoretical background and definitions [13], the ...
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 |
Citi izdevumi - Skatīt visu
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