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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 clinical trial from planning, conduct, interim analysis, final analysis and reporting. Services available include:

  •  Analysis of datasets
  • Statistical analysis complaint 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