From the development of the statistical analysis plan to the creation of the statistical analysis report, our experts analyze data relying on their knowledge and experience to rigorously assess drug efficacy and safety. Our experts have extensive experience in post-marketing surveillance and statistical analysis of data in all phases of clinical trials.
Our statistical expertise is comprehensive, supporting all aspects of clinical research, from protocol development to clinical study report writing. We exceed client expectations, and even provide statistical support for scientific journal writing. Double programming and checking, performed by our experienced programmers and data professionals, ensure the process, the quality of the analysis program, and the results. We can support various specialized initiatives including the Clinical Data Interchange Standards Consortium's (CDISC) standards, conduct various statistical methodologies and pharmacokinetic analyses. We can also perform highly accurate short-term analysis based on our extensive experience, and provide statistical expertise and recommendations for our clients' statistical needs. Through continuous education, we are committed to updating our knowledge in statistical techniques as applied to clinical research.
A full range of statistical analysis services that are your assurance of successful clinical trials.