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Do CROs Need to Reinvent Themselves in 2025? A Deep Dive with Greg Licholai and Derk Arts
High R&D costs aren’t due to a lack of innovation but inefficiencies in trials. Here’s how we can...
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
Enrollment, randomization and data cleanliness in dashboards that ship ready to use. Click any metric to land in...
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
Every field decision in the form editor shows up later as clean data or as a query. See...
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)
A coordinator's entry screen with real-time saving, so an interrupted session costs nothing, and edit checks that flag...
Randomization Module
Randomize inside the EDC as soon as the required fields are complete, with stratification, variable block sizes and...
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
What a participant sees on their own phone or a provisioned device, with invalid answers caught on their...
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)...
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