The University of Florida is seeking a cloud-based software solution to manage regulatory documentation and electronic consent for clinical trials. The selected vendor, Veeva Systems, Inc., will provide a solution that integrates with the university's clinical trial management system and other research applications. The contract has an initial period of three years with options to renew for up to two additional one-year periods. The university expects the solution to improve regulatory compliance, create operational efficiencies, and enhance the patient experience in clinical trial research. Key features of the solution include cloud-hosted, web-based SAML authentication, 21 CFR Part 11 capability, and the ability to integrate with UF's CTMS, OnCore, and other research applications.