Phase Iib-III Clinical Trials - Biostatistics and Statistical Programming
Statistical skills and experience. Precise analyses.
inVentiv Health Clinical biostatisticians have a broad knowledge base in all aspects of clinical trials, from the initial stage of planning the design and calculating sample size requirements, to analyzing, displaying and interpreting data in the final stages of the study. In addition, our biostatistics team has significant experience preparing analyses for regulatory submissions in a manner that facilitates their review. inVentiv Health Clinical experts plan the analyses you’ll need before the study begins, then provide reports, statistical summaries, and efficacy and safety analyses promptly and accurately as the study progresses.
We can leverage our vast statistical experience to design studies in a way that speeds submissions. Our thorough validation and quality control processes will eliminate the need for corrections and ensure accurate results. By applying standard templates and programs with customization as needed, we will provide efficient, high quality analyses for your project.
Biostatistics services include: