Our approach to reliable data begins with in-depth, cross-functional conversations to generate custom CRFs and SAPs.

Ongoing reviews, regular communication throughout the process, and extensive experience with regulatory compliant submissions ensure that when projects close out, our sponsors are satisfied with the integrity of our biostatistic deliverables.

Complex Efficacy Endpoints

Statistical Analysis Plans (SAPs)

Statistical Programming and Analysis

Tables, Listings, and Figures (TLFs)

CDISC-Compliant Datasets

Biostatistics Services

The Trialwise approach to quality data begins with cross-functional collaboration to design custom CRFs and SAPs for our sponsors early in the process. Advance development of the forms ensures collection of all critical variables at specified timepoints, and delivery of clean, accurate clinical data.

Ongoing reviews and regular communication throughout the study and extensive experience with regulatory compliant submissions ensure that when projects close out, our sponsors are satisfied with the integrity of our biostatistic deliverables.

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Thorough planning yields successful study execution.