Castor Essentials: The Fastest Route To Compliant Medical Device Trials

For lean clinical and regulatory teams, balancing compliance requirements with limited resources can be a challenge. Purpose-built for pilot, validation, 510(k), and CE mark studies, Castor Essentials combines electronic data capture and patient-reported outcomes in a single platform, helping teams avoid fragmented data and costly integrations. See how compliant study workflows can be configured without code through a live build demonstration, from designing eCRFs and ePROs to managing audit-ready data collection. Learn what 21 CFR Part 11 readiness looks like in practice, including the audit trails and controls required to support inspections and regulatory submissions.

Explore how a streamlined, self-service approach can help your team move from protocol to first patient faster.