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Castor ePro
Rapid, compliant, and scalable patient-reported data capture
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Castor ePro - 2026 Pricing, Features, Reviews & Alternatives
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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.
Key benefits of using Castor ePro
1. Unified Platform
Castor ePRO is fully integrated into Castor’s clinical data platform (EDC, eConsent, eCOA), allowing teams to manage all study data in one place—reducing errors, manual work, and vendor overhead.
2. Full-Service eCOA Delivery
Avoid vendor sprawl. Our team handles scale licensing, validated translations, device provisioning, and global patient support—so you don’t have to.
3. Rapid Study Deployment
Typical hybrid study builds (EDC, eConsent, ePRO + integrations) are delivered in 8–10 weeks. Faster setup means faster first patient in.
4. BYOD or Provisioned Devices
Support both bring-your-own-device and provisioned hardware strategies. Castor ensures secure, compliant access—online and offline.
5. Global Library of Validated Instruments
Access 120+ pre-validated PRO instruments, speeding up design and compliance. Ideal for trials requiring standardized assessments across multiple regions.
6. Multilingual, Direct-to-Patient Support
Provide patients with support in their own language. Our multilingual helpdesk improves engagement, retention, and data quality.
7. Designed for DCTs and Hybrid Trials
Castor ePRO is optimized for modern trial models—supporting fully remote, site-based, or hybrid designs with equal ease.
8. Compliance and Data Integrity
Fully validated platform meets 21 CFR Part 11, GDPR, and Good Clinical Practice requirements—ensuring audit readiness and data security.
9. Flexible Integrations
Easily connect to other systems and tools via API, enabling streamlined data exchange and automation where needed.
10. Scalable for Any Study Size
From small academic studies to global phase III trials, Castor ePRO scales to meet the needs of growing teams and complex protocols.
Starting price
Castor ePro’s user interface
Castor ePro reviews
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Typical customers
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Castor ePro FAQs
Castor ePro has the following typical customers:
Large Enterprises, Mid Size Business, Small Business
Q. What languages does Castor ePro support?
Castor ePro supports the following languages:
English
Q. Does Castor ePro offer an API?
Yes, Castor ePro has an API available for use.
Q. What level of support does Castor ePro offer?
Castor ePro offers the following support options:
Knowledge Base