ClinAsia Labs believes that biostatistics play a critical role in the planning and implementation analysis of clinical trials. This particular team is typically responsible for thoroughly analyzing clinical data and ensuring of generating reports for regulatory submission.

Services offered in this area include

• Successful recommendation strategy with regulatory authorities
• Preparation of Statistical analysis plans for clinical trials and formulation of Data Monitoring Committees
• Power calculation with defined sample size
• Designing and development of tables, graphs and listings
• Defining integrated summaries of safety and efficiency
• Complete statistical needs necessary for regulatory submissions
• Interim analyses, with an eye on impact of alpha
• Expert personnel to serve as statisticians on Data Monitoring Committees
• Supporting in the review of proposed analyses
• Designing and generation of in-text tables that supports clinical study reports