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The appropriate design of a clinical trial is essential, both to ensure that your trial leads to unbiased conclusions and that it is designed in accordance with ethical guidelines. Having a well-designed study is critical for preventing many problems at the data analysis stage. We are able to offer statistical services for the entire process of a clinical trial from planning, conduct, interim analysis, final analysis and reporting. Services available include:

  •  Analysis of datasets
  • Statistical analysis compliant with GCP and CDISC standards
  • Assistance with writing study protocols
  • Guidance on methodological issues, such as trial design, safety variables, and control groups
  • Assistance with writing statistical analysis plans
  • Guidance on statistical issues, such as sample sizes, appropriate use of statistical tests, and the adjustment for confounding variables