Merge ePRO™
Patient-Reported Outcomes by Device, Web, and Mobile Technology
Merge ePRO offers multiple, adaptable modalities for capturing electronic patient-reported outcomes (ePRO) for near real-time analysis. The result is high subject compliance and more reliable data across different therapies, populations and geographies.
Whether by device, web or phone, Merge ePRO provides best-in-class capabilities that are simple to use for subjects of all ages, and makes collecting patient-compliant data easy.
Merge ePRO provides:
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Improved patient compliance
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Rapid access to primary efficacy data from a patient perspective
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Greater accuracy of data—some treatment effects are known only to the patient
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Decreased data management cost (of data cleaning)
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Elimination of double data entry, illegible handwriting, measuring VAS scales with rulers and extraneous text or comments
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FDA recognition of the increasing clinical value of ePRO
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Full integration with Merge’s EDC, IVR/ IWR and Imaging Solutions
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Devices built on the industry-leading Windows® platform
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Predefined study questions that accelerate start-up time, and can be customized to meet specific study parameters
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ePRO by Windows devices, web or phone