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Castor ePro
Rapid, compliant, and scalable patient-reported data capture
Table of Contents
Castor ePro - 2026 Pricing, Features, Reviews & Alternatives
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Last updated: March 2026
Castor ePro overview
What is Castor ePro?
Castor ePRO enables fast, reliable collection of electronic patient-reported outcomes (ePRO) for clinical trials of any size or complexity. It’s part of Castor’s unified clinical data platform, which includes EDC, eConsent, and eCOA—all designed to support hybrid and decentralized trials.
What makes Castor stand out isn’t just the technology, but the service behind it. Our dedicated eCOA team delivers full operational support:
• Licensing and managing clinical outcome assessments
• Validated translations across 40+ languages
• Device provisioning and logistics
• Multilingual helpdesk and patient support
• Access to a global library of 120+ pre-validated PRO instruments
Whether you're running a global phase III study or a small digital trial, Castor eliminates the need for multiple vendors. We simplify compliance, improve patient engagement, and reduce the time it takes to go live—most studies are built and launched within 8–10 weeks.
Castor ePRO is fully validated and supports 21 CFR Part 11 and GDPR compliance. Use your own devices (BYOD) or provision devices through Castor, with full offline capability for remote environments.
If you’re looking for a scalable, full-service ePRO solution built for modern trials, Castor is your partner from startup to study closeout.
Starting price
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Castor ePro’s user interface
Castor ePro reviews
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Castor ePro's key features
Most critical features, based on insights from Castor ePro users:
All Castor ePro features
Castor ePro alternatives
Castor ePro
Starting from
No pricing info
NextGen Office
Starting from
300
RXNT
Starting from
29
/user
Per month
NextGen Enterprise
Starting from
No pricing info
Castor ePro support options
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