Being an ophthalmology-focused company, we continually leverage our depth of experience and data to give us insight into how to accelerate trials and ensure quality, while streamlining clinical operations.
We incorporate technologies that automate processes, comply with all required guidelines and regulations, and deliver an exceptional experience for our clients.
Ora utilizes the Veeva Vault platform as the foundation for our integrated systems approach to trial management. This includes CTMS, study start-up, monitoring, site payments, eTMF, and more.
Ora’s Veeva Vault platform performance is supported through existing integrations with our core EDC systems to equip project team with real-time, comprehensive, integrated data insights.
Ora’s Veeva CTMS start-up module is a multi-tenant cloud solution that unifies information and documentation for a single source of data across clinical operations.
Ora typically provides the electronic data capture (EDC) and interactive response technology (IRT) systems for studies and all associated services. We develop the study specific eCRFs and corresponding instructions, as well as customize the EDC/IRT platform, including testing and validation prior to FPFV.
With turn-key support systems in place, Clinical research gives you the opportunity to grow your practice and make a difference to those who matter most — patients.
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