Our expert biostatisticians and statistical programmers are skilled in the design and analysis of Phase I-IV clinical trials and health surveys. They will help you select the most appropriate design to meet the objectives of your study and the recommendations of all relevant regulatory bodies. Importantly, we will take into consideration the intended audience for your data, whether it be a regulatory agency, specific journal, market research group, abstract/podium, or internal proof-of-concept.
Whether the study design is parallel, factorial cross-over, sequential, Bayesian, or therapeutic equivalence, our team will use the latest and most appropriate statistical tools and techniques to maximize your data's potential. Our biostatisticians are SAS-certified and all of our statistical software is 21 CFR Part 11 compliant.
Our services include: