Castor eCOA delivers rapid, compliant, and scalable patient-reported data capture—whether you’re running traditional, hybrid, or fully decentralized trials. As part of Castor’s unified platform or as a standalone solution, eCOA enables sponsors and CROs to streamline the participant experience, ensure data integrity, and power confident clinical decisions.
With a footprint spanning 90+ countries, Castor has supported studies in:
We maintain a secure, globally distributed infrastructure that aligns with regional data protection laws and regulatory guidelines, including GDPR, HIPAA, and applicable data privacy laws in APAC, LATAM, and EMEA. Castor supports data localization where required and ensures full compliance with global privacy standards through ISO 27001-certified hosting environments.
Castor eCOA has been deployed successfully across high-complexity and high-sensitivity indications. Our experience spans:
These studies often involve vulnerable populations, demanding precise, intuitive, and engaging eCOA solutions—all supported by Castor’s configurable platform and expert services.
Castor’s eCOA is built on the principles of interoperability, transparency, and speed. Designed for modern trial delivery models, Castor supports:
Castor’s API-first technology enables the development of eCOA solutions that are fit-for-purpose for any protocol—from early-phase proof-of-concept to multinational pivotal studies.
Castor’s eCOA is not a separate add-on—it’s natively integrated with our EDC, eConsent, and eCOA platform. All participant data flows seamlessly into a single system in real-time—no third-party syncs, no manual uploads, no fragmented data.
Castor combines the innovation of an API-first platform with the practical needs of global trial operations, delivering accelerated time to value through rapid deployment and seamless integration. Whether you’re running a Phase I dose escalation in a single country or a global DCT across 10+ regions, Castor eCOA empowers you to:
Next Steps Checklist