Cedent biostatisticians are highly experienced 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.

Cedent experts plan the analyses you’ll need before the study begins,then providereports, statistical summaries, and efficacy and safety analyses promptly and accurately as the study progresses.