Our expert team provides support in the early stages of protocol development, with sample size calculation and randomization algorithms. During data collection, our team can provide interim analysis services and sample size re-estimation calculations and randomization list extensions, as well as statistical analysis planning. After data collection, we provide a full statistical programming and analysis services, together with reporting.

Every service we provide is conducted by expert biostatisticians and clinical programmers with many years of experience in clinical trials. All our processes are completed with our extensive QA/QC processes.

Thanks to the amazing collaborative strength between data managers and medical writers, biostatisticians, and clinical programmers, statistical programming and preparatory activities are conducted while data collection is ongoing. This significantly reduces timelines for statistical deliverables after database lock and export.

Ensuring regulatory compliance in statistical analysis is our priority. Rigorous validation processes, aligned with our company's high standards and industry-leading regulatory validation programs, are integral to our practices. All our statistical processes are aligned with regulatory guidelines and recommendations, including ICH E9, among others sounds smoother. Additionally, our biostatisticians and statistical programmers are true scientists with PhD degrees, and perform literature reviews for state-of-the-art procedures and continuous education.