Biostatistics
At Hekma Clinical Research, our Biostatistics Division is comprised of industry-leading statisticians and clinical research experts dedicated to transforming complex data into clear, actionable insights. We partner with you at every stage of your clinical trial to ensure robust, statistically sound outcomes that meet global regulatory standards.
Our Comprehensive Biostatistics Services Include:
- Statistical Consultancy – Expert guidance tailored to your study’s unique requirements
- Study Design & Protocol Development – Optimized trial frameworks for maximum efficiency and compliance
- Sample Size Estimation & Power Calculations – Scientifically validated methods to ensure study adequacy
- Endpoint Selection & Hypothesis Formulation – Strategic alignment with study objectives and regulatory expectations
- Advanced Randomization Procedures – Innovative techniques for balanced treatment allocation
- Statistical Analysis & Interpretation – Rigorous methodologies using industry-leading software (SAS, SPSS, Stata, R)
- Regulatory-Compliant Report Writing – Clear, comprehensive documentation of methods and findings
- Start-Up Phase Support – Seamless integration of statistical planning from trial initiation
Statistical analyses are performed using different softwares including industry standard SAS, SPSS and Stata software. Our Standard Operating Procedures guarantee high quality results. The results are presented in a statistical report describing the analyses performed and providing an interpretation of the results.