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Join Castor at ACDM 2025 in Prague to explore innovations in RWE, EDC, ePRO, and eConsent. Book a meeting with our team!

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Castor CDMS with integrated ePRO streamlines patient-reported outcome management by enabling study coordinators to send, track, and review surveys efficiently.

Castor’s interactive dashboards provide real-time tracking of key study metrics.

Scheduling a televisit in Castor is quick and intuitive—users can create an appointment within the televisit planner by defining the session details, date, time, duration, and attendees.

Castor has announced free access to its clinical trial technology platform for U.S. researchers impacted by recent NIH funding cuts. Through the Castor for Impact Program, investigators can maintain data integrity, streamline workflows, and keep projects moving forward, despite reduced indirect cost allocations threatening vital scientific progress and ongoing discovery.

With Castor CDMS, lead clinical data managers and study administrators can efficiently build electronic case report forms (eCRFs) while ensuring data accuracy and usability.

Castor’s data export functionality provides real-time access to study data in multiple formats, including CSV, Excel, SPSS, SAS, and CDISC ODM, ensuring compatibility with analytical tools.

Castor’s data import feature simplifies adding participant data by seamlessly matching CSV file inputs to predefined study variables, reducing manual entry.