Betekenis van:
trueness

Voorbeeldzinnen

1. ISO 5725-1, Accuracy (trueness and precision) of measurement methods and results.
2. Estimation of the analytical trueness, recovery calculations and reporting of results
3. ISO 5725-1: Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions.
4. ISO5725-1: Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions.
5. ‘Trueness. It shall be ensured that the emission determination is systematically neither over nor under true emissions.
6. High accuracy (trueness and precision). The determination shall provide a valid estimate of the true concentration in a sample.
7. ISO 5725-1, Accuracy (trueness and precision) of measurement methods and results. Part 1: General principles and definitions.
8. ISO 5725-1: Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions. Geneva, 1994.
9. ISO 5725-2, Accuracy (trueness and precision) of measurement methods and results. Part 2: A basic method for the determination of repeatability and reproducibility of a standard measurement method.
10. The average within laboratory standard deviation, calculated from results generated under repeatability conditions as defined in ISO standard 5725-1 [1] ISO 5725-1: Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions.
11. The between laboratory standard deviation, calculated from results under reproducibility conditions as defined in ISO standard 5725-1 [1] ISO 5725-1: Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions.
12. Accuracy is expressed as trueness (difference between the mean value measured for an analyte in a certified material and its certified value, expressed as percentage of this value) and precision (RSDR relative standard deviation calculated from results generated under reproducibility conditions).
13. ‘full validation procedure’ means the assessment through a ring trial involving national reference laboratories of the method performance criteria set by the applicant as compliant with the document entitled ‘Definition of minimum performance requirements for analytical methods of GMO testing’ referred to in point 1(B) of Annex I to Regulation (EC) No 641/2004, and the assessment of the repeatability and trueness of the method provided by the applicant;