Helping sponsors and sites manage clinical trials to accelerate the development of new medicines and therapies.
The only research system designed to work in a real-world healthcare environment, it collects data at the point of care using CDISC global research data standards and automatically prepares it for regulatory compliance and submission while:
Prioritizing data interoperability
Promoting study efficiency by automating administrative tasks
Providing all stakeholders with real-time transparency into the patient’s entire journey
Maintaining the integrity of the trusted physician and patient relationship
End-to-End Clinical Trial Support
Rely on IntElligo for quality oversight, real-time transparency, and paperless study conduct.