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 80.
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... & production GmbH , Heidelberg Production : LE - TEX Jelonek , Schmidt & Vöckler GbR , Leipzig Printed on acid - free paper 52 / 3111 / YL - 543210 Different approaches to legal requirements on validation of test methods.
... & production GmbH , Heidelberg Production : LE - TEX Jelonek , Schmidt & Vöckler GbR , Leipzig Printed on acid - free paper 52 / 3111 / YL - 543210 Different approaches to legal requirements on validation of test methods.
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... test ............... 121 51 Method validation and reference materials ........... 128 Analytical validation in ... methods. General principles and concepts ......................................... 139 62 Validation requirements for chemical ...
... test ............... 121 51 Method validation and reference materials ........... 128 Analytical validation in ... methods. General principles and concepts ......................................... 139 62 Validation requirements for chemical ...
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... AOAC's three validation systems 163 Observing validation, uncertainty determination and traceability in developing Nordtest test methods...... 167 DOI 10.1007/s00769-002-0516-5 © Springer-Verlag 2002 Frank T. Peters Hans H. VIII Contents.
... AOAC's three validation systems 163 Observing validation, uncertainty determination and traceability in developing Nordtest test methods...... 167 DOI 10.1007/s00769-002-0516-5 © Springer-Verlag 2002 Frank T. Peters Hans H. VIII Contents.
3. lappuse
... methods which pro- duce a response for a single analyte , whereas ... analysis of up to 20 blank samples spiked with analyte at the lower limit of ... test [ 6 , 9 ] . A detailed discussion of alternative statistical tests for ...
... methods which pro- duce a response for a single analyte , whereas ... analysis of up to 20 blank samples spiked with analyte at the lower limit of ... test [ 6 , 9 ] . A detailed discussion of alternative statistical tests for ...
4. lappuse
... test results and an accepted reference value [17]. It may consist of more ... method validation, but rather from the results of a great number of quality ... methodology) [13]. Repro- ducibility only has to be studied, if a method is ...
... test results and an accepted reference value [17]. It may consist of more ... method validation, but rather from the results of a great number of quality ... methodology) [13]. Repro- ducibility only has to be studied, if a method is ...
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