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The data of this validation study showed that CZE is a reliable assay for the determination of protein composition in therapeutic preparations of human albumin and human polyclonal immunoglobulins.
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The predictive performance of this schedule was prospectively evaluated using the data of the validation group.
These two schedules (i.e. 1.5 4 6 and 1.5 6) were evaluated prospectively using the data of the validation group.
The data of this series of validation studies are compared to the ENGL method performance requirements and the results are analysed to determine the relative contribution of the different aspects of the test procedure to the variation.
Being aware that there are multiple mechanisms of liver toxicity leading to a variety of perturbations in gene expression, there is a need for validation of the data of this feasibility study.
In this stage, the data of the training and validation data sets of the FINO 1 platform are considered (see Figure 7b).
In this stage, the data of the training and validation data sets of the Ekofisk platform (see Figure 7a) are considered.
Some of the data used in this validation were assessed by CATI with the family caregivers.
The gold standard for doing this is to set aside a portion of the data for this final validation step (the so-called test set validation).
The data quality of the validation experiments described in this paper proved to be satisfactory, while at same time a maximum amount of data was preserved.
Data on age has been altered to reflect the actual age at the time of data collection in this validation study.
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