Biostatistics

Biostatistics and pharmacokinetics support throughout development

Our experienced biostatisticians, statistical programmers and pharmacokinetic analysts enable Nuvisan to provide highest-quality design and analysis of early-phase clinical trials that are both scientifically sound and compliant with regulatory standards, maximising the chances of success for your clinical development program. As a team of dedicated scientists, Nuvisan provides comprehensive support for statistical and pharmacokinetic consultancy from trial design to reporting.

Critical thinking at every step

Our biostatisticians provide tailored advice based on your specific needs at every critical stage, from the earliest phases of clinical development planning to the final presentation of data. We offer expert guidance to optimise the statistical design and analysis of studies across a wide range of development phases, whether for our in-house clinical trials or stand-alone biostatistical or pharmacokinetic services requests. Our in-house team is co-located with all Nuvisan clinical services teams (project management, medical writing, medical experts, Clinical Pharmacology Unit, data management and monitoring), to help ensure quick and effective communication for all aspects of your project.