With our fully configurable ePRO/eCOA solution, we help assure your team gets the highest quality patient-reported outcomes for your study. The movement from paper-based to ePRO data capture has enhanced the integrity and accuracy of clinical trial data and is encouraged by regulators.
We offer flexible, automated notifications and robust patient reported outcome tools that give you more accurate and complete data. Here are some reasons why our clients utilize our platform, and solutions.
Clinical StudyPal meets all global regulations for collecting clinical trial data including ICH/GCP, 21 CFR, GDPR, and HIPAA.
More about our capabilities – we can utilize home clinical visits (using a network of 1million nurses) and mobile application technology to screen and gain consent from patients using video-conferencing, and allowing nurses collect data through an app and supplying patients with ePROs
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REAL-TIME DATA COLLECTION FOR PRIME-TIME OUTCOME ASSESSMENTS
With our fully configurable ePRO/eCOA solution, we help assure your team gets the highest quality patient-reported outcomes for your study. The movement from
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