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 66.
. lappuse
... method for the determination of p -dichlorobenzene and naphthalene in mothrepellents.. 80 Validation of ... Analytical validation in practice at a quality control laboratory in the ... procedure in terms of measurement (quality) assurance ...
... method for the determination of p -dichlorobenzene and naphthalene in mothrepellents.. 80 Validation of ... Analytical validation in practice at a quality control laboratory in the ... procedure in terms of measurement (quality) assurance ...
2. lappuse
... method validation are the different sets of terminolo- gy employed by ... method validation. Furthermore, the ICH definition of selectivity did not take into account ... Analytical Methods Validation: Bioavailabil- ity, Bioequivalence and ...
... method validation are the different sets of terminolo- gy employed by ... method validation. Furthermore, the ICH definition of selectivity did not take into account ... Analytical Methods Validation: Bioavailabil- ity, Bioequivalence and ...
6. lappuse
... method can only produce semiquantitative or qualitative data. However, it can ... procedure is a prerequisite for reliable quantifica- tion. Therefore, full ... analytical run). One should also test the stability in prepared samples un ...
... method can only produce semiquantitative or qualitative data. However, it can ... procedure is a prerequisite for reliable quantifica- tion. Therefore, full ... analytical run). One should also test the stability in prepared samples un ...
10. lappuse
... analytical procedure on the analytical results obtained by the method. In this way signifi- cant changes in the results may be caused only by replacement of the previous program by the new one. Table 1 Results of the experiment (average ...
... analytical procedure on the analytical results obtained by the method. In this way signifi- cant changes in the results may be caused only by replacement of the previous program by the new one. Table 1 Results of the experiment (average ...
11. lappuse
... analysis, commonly acceptable as the simplest, were chosen for minimising the influence of all the steps of the analytical procedure on the analytical results. These objects are aqueous so- lutions of lead for the graphite furnace, of ...
... analysis, commonly acceptable as the simplest, were chosen for minimising the influence of all the steps of the analytical procedure on the analytical results. These objects are aqueous so- lutions of lead for the graphite furnace, of ...
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