{ PK/PD Analysis and Statistics }
Determination of the effects of dose, formulation, dosing regimen, drug interactions, genotype, gender, and other factors in pharmacokinetics are made clear and understandable by the biostatistical staff of DaVita Clinical Research (DCR). Providing guidance and input throughout the process, the staff offers statistical analysis of the safety and efficacy of the pharmacokinetic data, as well as the charts, tables, and data.
Capabilities include:
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Writing and documenting validated SAS programs for data analysis and reporting
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Selection of appropriate statistical methods
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Generation of randomization schedules
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Defining analysis populations
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Sample size rationale
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Description of statistical methodology
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Identifying outliers
