cOS Trials

cOS™ Trials is a multi-site HIPAA and FDA 21 CFR Part 11 compliant, integrated system that enables clinical research organizations to:

• prepare study budgets
• set up study protocols, calendars and milestones
• manage adverse events and IRB submissions
• manage and schedule subjects
• deploy electronic data capture at research sites
• compile case report forms (CRFs) electronically
• generate invoices and payouts automatically.
• provide value-added information service to their sponsors, and share vital study results such as efficacy and adverse events electronically through a web portal. 

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cOS Trials is powered by Velos and the Net.Orange cOS.