¡°³Ô¹Ï±¬ÁÏ helps our clinical operations teams execute studies in less time. Now we can manage information and end-to-end trial processes, from site activation to study closeout, all in one platform.¡±

Ed Leftin, Director, Information Systems

One system, one process, one view across the clinical trial portfolio
One system, one process, one view across the clinical trial portfolio
Better, more informed decision-making and proactive trial management
Better, more informed decision?making and proactive trial management
Reduced study closeout time from weeks to days
Reduced study closeout time from weeks to days

1

Speed global site selection and activation with ³Ô¹Ï±¬ÁÏ Study Startup

³Ô¹Ï±¬ÁÏ Study Startup¡¯s built-in country intelligence helps Ora manage a growing number of global sites, each with its own unique set of documents and activities required for activation.

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2

Stay inspection ready with ³Ô¹Ï±¬ÁÏ eTMF

Ora¡¯s clinical teams manage documents and processes in real-time as the TMF is generated, improving inspection readiness and reducing study close?out time from weeks to days.

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3

Empower teams with greater insights across the trial lifecycle with ³Ô¹Ï±¬ÁÏ CTMS

“We now have best-in-class ³Ô¹Ï±¬ÁÏ applications and integration technology to optimize clinical delivery and strengthen relationships with our clients.¡±
Ed Leftin, Director, Clinical Systems

Read the Case Study

4

Simplify clinical research site payments with ³Ô¹Ï±¬ÁÏ Payments

Ora eliminates manual processes, improving payment efficiency and accuracy.

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Bringing it all together: ³Ô¹Ï±¬ÁÏ Clinical Platform improves study execution and quality

¡°The value of a unified clinical platform is the impact it has on our users. It¡¯s one system; it¡¯s one data repository.¡±
Ed Leftin, Director, Information Systems

Resources

See a 4-minute overview of the ³Ô¹Ï±¬ÁÏ Clinical Operations
Demo See a 4-minute overview of the ³Ô¹Ï±¬ÁÏ Clinical Operations
Read the ³Ô¹Ï±¬ÁÏ Annual CRO Report
Webpage Learn how CROs are paving the way for digital trials