Proactive involvement of our biostatisticians results in the efficient and accurate collection, analysis and interpretation of clinical study data. Our biostatisticians take part in prospectively defining study objectives and selecting the most appropriate study design, inclusion criteria, sample sizes, clinical endpoints and statistical analyses.
Unique among contract researchers, Frontage ensures all programming code is independently validated in parallel to detect possible errors.
Also different is the way Frontage provides flexibility in data reporting. Clients can request standard reporting or custom reporting, which enables integration with their existing systems and processes.