You can use Florence Healthcare to manage clinical trial workflows and regulatory documents across research sites and sponsors. It digitizes investigator site files, participant binders, and logs while supporting remote monitoring for clinical research organizations. Research teams can exchange trial documents, track study startup progress, review contracts, and capture digital patient consent. The system provides audit trails and regulatory compliance tracking throughout each study phase. You can also archive completed trials securely for up to 25 years while retaining full search and export capabilities.
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