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.

Enhance your clinical trials from feasibility through submission with this healthcare-enabling workflow tool.  

  • Expedited patient identification and engagement  
  • Simple, standard, and rapid patient source data collection 
  • Real-time data updates and analytics 
  • Efficient study operations

Attention experienced and new to research sites:

The IntElliGo Study Marketplace makes it easy to build and manage a study pipeline, accelerating your participation in clinical research.

From supporting remote monitoring in decentralized clinical trials to increasing patient centricity, IntElligo accelerates and enhances your entire study. 

  • Rapid enrollment  
  • Improved data transparency and quality  
  • Heightened clinical trial management  
  • Accelerated study financials processes 

Increase Collaboration, Efficiency, and Oversight From Patient ID Through Study Close.

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