Our Clinical Biostatisticians and Programmers bring comprehensive biomedical expertise specifically tailored to your unique study. Direct study design and detailed process organization are the foundation of our approach to all programs.
• Protocol development and clinical planning• Statistical consulting and analysis• Randomization• Sample size determination• Data safety committees• Report-ready analysis tables• FDA representation/assistance
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“I have worked with Prosoft Clinical on multiple projects from Phase 1 through Phase 3 over the past several years and have used partial service to full service depending on the project. Prosoft Clinical’s team performs as if they were part of your own organization which I think sets them apart from other CROs. They are easy to work with no matter the scope of their services.
We have had to have them rescue projects awarded other organizations in order to get the job done and meet timelines.
Unlike some of the other CROs you aren’t nickled and dimed with change orders.
Prosoft Clinical’s edc system is easy to use for both the sponsor and site personnel.
Prosoft Clinical’s team has many years of experience working on the Sponsor side of the business so they understand their customers.”