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We provide experienced licensed clinical staff at a subsidized cost for the timely launch of your research study. Our list of services includes the onsite organization of logistics, detailed explanation of the launch process of a new clinical study, legal documents and submissions needed for IRB submissions, Seamless and speedy launch of IRB-approved clinical studies, availability of licensed and experienced healthcare staff for initial study launch support and training of permanent study team. Minimizing study deviations by assisting the study team, Ensuring that clinical studies are completed and endpoint data collected, Helping the study team in training for electronic data collection