Nitrosamine Impurities Affecting Drug-Drug Interaction Studies – Learn More


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Biostatistics Services for Optimal Trial Outcomes

You can rely on our team of high-qualified statisticians to provide the support your clinical study needs to mitigate risk and optimize outcomes. Our statisticians are intricately involved in study design, CRF design, data import/export, data cleaning and review, statistical analysis plans, and analyses, and are often consulted to perform special calculations and summarizations of information for non-study-related issues.

Our SAS programmers perform statistical and data programming in addition to providing tables, figures and listings (TFLs) based on the analyses and format specified in the statistical analysis plan, following either our standards or your specific requirements.

To ensure on-time delivery of quality data, we developed standard SAS programs and analysis codes that include a large number of macros to generate SAS output and streamline data delivery. In addition, data flow within our systems (clinical, bioanalysis and PK/biostatistics) is automated and error proof, streamlining efficiency and minimizing risk.

Renal / Hepatic Impairment’s Effect on the PK of Cabozantinib

Gain insight into renal and hepatic impairment’s effect on the PK of cabozantinib

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