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 38.
. lappuse
... International Vo- cabulary of Basic and General terms in Metrology ( VIM ) ( 1993 ) , surprisingly we do not find a definition . Webster's Dictionary of the English language ( 1992 ) tells us that val- idation is ' making or being made ...
... International Vo- cabulary of Basic and General terms in Metrology ( VIM ) ( 1993 ) , surprisingly we do not find a definition . Webster's Dictionary of the English language ( 1992 ) tells us that val- idation is ' making or being made ...
1. lappuse
... International Asso- ciation of Forensic Toxicologists (TIAFT; TIAFT Bulletin 32 (2002): 16–23) and of the Society for Forensic and Toxicologic Chemistry (GTFCH; Toxichem and Krimi- tech 68 (2001): 116-126). F.T. Department Peters ...
... International Asso- ciation of Forensic Toxicologists (TIAFT; TIAFT Bulletin 32 (2002): 16–23) and of the Society for Forensic and Toxicologic Chemistry (GTFCH; Toxichem and Krimi- tech 68 (2001): 116-126). F.T. Department Peters ...
2. lappuse
... International Conference on Har- monisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and approved by the regulatory agencies of the European Union, the United States of America and Japan. The ...
... International Conference on Har- monisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and approved by the regulatory agencies of the European Union, the United States of America and Japan. The ...
4. lappuse
... International Organization for Standardization (ISO) [17]. However, it must be mentioned that accuracy is often used to describe only the systematic error component, i.e. in the sense of bias [1, 2, 6–8, 10, 12, 13]. In the following ...
... International Organization for Standardization (ISO) [17]. However, it must be mentioned that accuracy is often used to describe only the systematic error component, i.e. in the sense of bias [1, 2, 6–8, 10, 12, 13]. In the following ...
7. lappuse
... international confer- ence and easily available on the homepage of ICH (www.ich.org). As already mentioned above, recovery is not among the validation parameters regarded as essential by the Con- ference Reports. Most authors agree ...
... international confer- ence and easily available on the homepage of ICH (www.ich.org). As already mentioned above, recovery is not among the validation parameters regarded as essential by the Con- ference Reports. Most authors agree ...
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