Biostatistical Analysis & Clinical Analysis

Our biostatistical services have you covered no matter what kind of clinical trial you have.  We can theoretically enter into collaboration at any stage of your research, whether the design stage, data collection, statistical analysis, reporting, and preparing for presentations. Our statisticians have vast experience either in the private or public sectors. The team is constantly updated with the cutting-edge statistical methodology to meet regulatory requirements. We have a wide range of biostatistical tasks and services designed to support your development program, such as:

  • Devise appropriate study designs (one arm, two-arm studies, adaptive design, seamless phase I/II, cross-over, etc.)
  • Sample Size Assessment
  • Randomization
  • Statistical Analysis Plan (SAP) – Outlining appropriate data-analytic strategies and tests
  • Statistical analyses
  • Statistical summary and Interpretation of study results
  • Review protocol and Statistical Analysis Plan for comparative efficacy and safety of biologics and biosimilar
  • Prepare for committee meetings
  • Prepare and revision manuscripts
  • Ongoing and general statistical consulting – problem-solving
  • SAS programming support (ADaM, SDTM, etc.)
  • Synthetic and External Control Arms design and analysis
  • Statistical programming through R or SAS
  • Statistical support for grant submissions
  • Statistical analysis and consultation