Solving eCOA Challenges in Clinical Trials

Collecting quality clinical outcome assessment data is often one of the most important and challenging parts of a clinical trial. Suvoda eCOA makes it easier and more efficient to get quality patient outcomes data with expert guidance, ClinRO and PRO questionnaire reusability, fast overall eCOA set up, and easy-to-use clinical trial tech.

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Suvoda eCOA supports sponsors and CROs to:

  • Streamline questionnaire licensing and localization
  • Improve clinical trial patient engagement with a user-friendly ePRO experience
  • Generate reliable and accurate clinical trial data with easy integrations
  • Empower sites with well-designed ClinRO technology 


Sponsors can partner with Suvoda’s scientific advisors and licensing experts to guide eCOA implementation. With support for BYOD and provisioned devices, site teams will find the complex logistics of getting the right questionnaires to the right patient at the right time are easily and securely managed—just like the drug supply in our IRT system. And just like IRT and eConsent, Suvoda eCOA is supported by our intuitive user experience, standard and ad-hoc reporting, and customer support.

 

Solving eCOA Challenges in Clinical Trials

Collecting quality clinical outcome assessment data is often one of the most important and challenging parts of a clinical trial. Suvoda eCOA makes it easier and more efficient to get quality patient outcomes data with expert guidance, ClinRO and PRO questionnaire reusability, fast overall eCOA set up, and easy-to-use clinical trial tech.

Suvoda eCOA supports sponsors and CROs to:

  • Streamline questionnaire licensing and localization
  • Improve clinical trial patient engagement with a user-friendly ePRO experience
  • Generate reliable and accurate clinical trial data with easy integrations
  • Empower sites with well-designed ClinRO technology 


Sponsors can partner with Suvoda’s scientific advisors and licensing experts to guide eCOA implementation. With support for BYOD and provisioned devices, site teams will find the complex logistics of getting the right questionnaires to the right patient at the right time are easily and securely managed—just like the drug supply in our IRT system. And just like IRT and eConsent, Suvoda eCOA is supported by our intuitive user experience, standard and ad-hoc reporting, and customer support.

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Schedule a Demo with our Experts
Suvoda eCOA was incredibly easy for our patients to use; we had an increase in patient compliance in completing PRO questionnaires, as compared to previous studies with other eCOA providers.”
Catherine Munera, Vice President of Biometrics, Cara Therapeutics

User Experience

100% of usability testers had an easy time navigating Suvoda eCOA

Design

100% of usability testers were happy with the visual experience

Device

93% of usability testers appreciated touchscreen responsiveness and ease-of-use

 

Andrés Escallón
Vice President, eCOA Practice
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Jill V. Platko, PhD
Vice President, Scientific Services
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Emily Potz
Director, Licensing & Localization
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Roger Vaillancourt
Director, eCOA Operations
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Amanda Howley
Director, eCOA Services Delivery
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Please share your contact information

Schedule a Demo with our Experts

Please share your contact information

Schedule a Demo with our Experts