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real-time outcomes
clinical trial patient reported outcomes

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.

  • Improved data integrity.
  • Real-time insights.
  • More accurate data collection, at the right time.
  • Better patient compliance.
  • Unified solution that provides patient engagement across our mix of Decentralized Solutions.
  • 24/7 patient concierge service to help improve compliance.

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

Get your demo today. Click here

Calendar: https://calendly.com/delvehlth/30min

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