Results (
Indonesian) 1:
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Precision. A detailed summary of the intra andinterday precision data generated for the assay validation is presented in Table 5. The inter and intradayprecision was <2% for all QC concentrations, whichwas within the general assay acceptability criteria forQC samples.Carryover test. In this analysis no quantifiable carryover effect was observed when a series of blank(plasma) solutions were injected immediately following the highest calibration standard.Ruggedness and robustness. The ruggedness wasestablished by determining the concentrations ofrifampicin, isoniazid and pyrazinamide by two differ
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