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 24.
. lappuse
... vali- dated measurement result , i.e. a quantity value1 with asso- Contents Bioanalytical method validation and its implications for forensic and. ciated measurement uncertainty ? The answer must be : no . There can never be a mechanism ...
... vali- dated measurement result , i.e. a quantity value1 with asso- Contents Bioanalytical method validation and its implications for forensic and. ciated measurement uncertainty ? The answer must be : no . There can never be a mechanism ...
7. lappuse
... vali- dation in forensic and clinical toxicology and add slight During pharmacokinetic studies (therapeutic) drugs are usually ingested under controlled conditions. Therefore, there is no need to prove the ingestion of this drug. Due to ...
... vali- dation in forensic and clinical toxicology and add slight During pharmacokinetic studies (therapeutic) drugs are usually ingested under controlled conditions. Therefore, there is no need to prove the ingestion of this drug. Due to ...
8. lappuse
... vali- dation discussed in this review. One probable reason might be that measurement uncertainties of modern ana- lytical methods are certainly small compared to the dif- ferences encountered between individual subjects in ...
... vali- dation discussed in this review. One probable reason might be that measurement uncertainties of modern ana- lytical methods are certainly small compared to the dif- ferences encountered between individual subjects in ...
10. lappuse
... vali- dation of the instrument, computer system, software and programs. On the other hand, the same instrument may also be calibrated and validated as a smaller (in- The positive validation conclusion was based on the comparison of the ...
... vali- dation of the instrument, computer system, software and programs. On the other hand, the same instrument may also be calibrated and validated as a smaller (in- The positive validation conclusion was based on the comparison of the ...
11. lappuse
... vali- dating the new program GIRAF for atomic absorption analysis with the Perkin-Elmer 5000 spectrophotometer equipped with the graphite furnace and/or flame facili- ties. The program was developed by Tech Projects ac- cording to ...
... vali- dating the new program GIRAF for atomic absorption analysis with the Perkin-Elmer 5000 spectrophotometer equipped with the graphite furnace and/or flame facili- ties. The program was developed by Tech Projects ac- cording to ...
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