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The accuracy of the method was determined by recovery experiments.
The accuracy of the method was determined as recovery by standard addition method.
The sensitivity of the method was determined with respect to LOD, LOQ, and correlation coefficient.
Ruggedness of the method was determined by using mobile phase components from two different manufactures.
Repeatability and reproducibility of the method was determined using intra and inter-day analysis.
Repeatability and reproducibility of the method was determined using inter and intra-day analysis.
The precision of the method was determined by assessing repeatability and reproducibility, expressed as RSD % values.
The reproducibility of the method was determined by five replicate injections performed within 3 days.
Sensitivity of the method was determined using a reverse-genetic H5N1 virus.
Reproducibility of the method was determined using field duplicates and blanks.
The recovery of the method was determined by adding a known amount of the drug to the standard concentration.
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