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Castor Helps Power the WHO Solidarity Trial Against COVID-19
Learn how Castor was instrumental in meeting the World Health Organization's need for a rapidly-deployable, scalable EDC solution...
Castor eConsent: Streamlined Participant Onboarding for Trials
Download our eConsent factsheet to view an overview of our services.
ePRO Site Coordinator
Castor CDMS with integrated ePRO streamlines patient-reported outcome management by enabling study coordinators to send, track, and review...
CDMS Study Dashboards
Castor's interactive dashboards provide real-time tracking of key study metrics.
CDMS Televisits
Scheduling a televisit in Castor is quick and intuitive—users can create an appointment within the televisit planner by...
Castor Steps Up to Preserve Critical Research Amid NIH Funding Cuts
Castor has announced free access to its clinical trial technology platform for U.S. researchers impacted by recent NIH...
CDMS Study Build
With Castor CDMS, lead clinical data managers and study administrators can efficiently build electronic case report forms (eCRFs)...
CDMS Data Export
Castor's data export functionality provides real-time access to study data in multiple formats, including CSV, Excel, SPSS, SAS,...
CDMS Data Import
Castor's data import feature simplifies adding participant data by seamlessly matching CSV file inputs to predefined study variables,...
CDMS Data Entry (Site View)
Castor CDMS streamlines clinical data collection, helping research teams capture high-quality data efficiently.
Randomization Module
Castor CDMS includes a validated variable block randomization module, enabling dynamic participant randomization directly within the platform.
Oncology factsheet
Download our oncology factsheet to view an overview of our services.
Real-world evidence factsheet
Download our RWE factsheet to view an overview of our services.
How Advanced Neuromodulation Researchers Cut Study Build Time by 63% Using Integrated Trial Technology
This detailed case study reveals the practical strategies and technology solutions that enabled researchers to automate participant screening,...
Participant View eCOA | ePRO
Reduce participant and site burden with a simple 2 step onboarding and user-friendly app. Secure questionnaires via email...
eCOA/ePRO factsheet
Download our ePRO/eCOA factsheet to view an overview of our services.
Clinical Trials Aren’t Just About Patients (and That’s Okay)
This article explores the debate between patient-centricity and protocol-centricity in clinical trials, featuring insights from Derk Arts (Castor)...
Strategies to Minimize Participant and Healthcare Provider Burden in Clinical Trials
This article examines strategies to reduce participant and provider burden in clinical trials while ensuring high-quality data collection....
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