Study insights, always close at hand.

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.

  • Faster trials: Real-time, actionable insights into trial status improve efficiency and performance.
  • Better decision making: A full view of your global operations in a single system enables more strategic trial planning.
  • Streamlined clinical operations: By unifying trial information and proactively identifying site issues, we eliminate manual processes and enable better study management.

All the information in one place.

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.

  • Sponsors, CROs and investigators have access to clinical master data with a single system of record for study, country, and study site information.
  • During studies, Ora will provide training to the sites and access to a 24/7 helpdesk for sites should any support be needed.
Real-time visibility for rapid acceleration

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.

  • Available EDC/IRT platforms through Ora include iMedNet and Medidata systems.

  • Due to our depth of experience, we have a robust library of ophthalmology-based eCRFs to support your eCRF design process.

Take your practice to the next level with Ora.

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.

For over 45+ years, Ora has been on the leading edge of ophthalmic product development.

When your product shows promise, let's prove it.

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