Demos13 March 2025 Flexible Remote DCT – Site View Castor offers flexible and tailored solutions for clinical trials, from patient recruitment landing pages to automated screening and consent workflows. Learn more
Demos13 March 2025 Flexible Remote DCT – Patient View Flexible Remote DCT allows patients to participate in decentralized clinical trials (DCTs) from anywhere, offering convenience and reducing the need for site visits. Learn more
Blog13 March 2025 The Catch-22 of eConsent: The Missed Opportunity for Improved Clinical Trials It’s time to move beyond digital PDFs. Discover how real eConsent can transform trials, reduce dropout, and respect autonomy for all. Learn more
Video7 March 2025 Castor CDMS 2025.1 New Release Castor’s Q1 2025 release boosts clinical trial management with improved reports, a modern UI, and enhanced Form Builder features—see the full notes online Learn more
Blog27 February 2025 Build vs. Buy vs. Partner in Life Sciences: Making the Right Call How do you decide between building, buying, or partnering? Learn key decision factors and red flags to avoid costly missteps. Learn more
Blog26 February 2025 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 fix the system. Learn more
Event21 February 2025 ACDM25 Meet us at Booth #10 March 2nd – 4th, 2025 | Clarion Congress Hotel, Prague Join Castor at ACDM 2025 in Prague to explore innovations in RWE, EDC, ePRO, and eConsent. Book a meeting with our team! Learn more
Success Stories19 February 2025 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 with advanced functionality. Learn more
Factsheets18 February 2025 eConsent factsheet Download our eConsent factsheet to view an overview of our services. Learn more
Demos17 February 2025 ePRO Site Coordinator Castor CDMS with integrated ePRO streamlines patient-reported outcome management by enabling study coordinators to send, track, and review surveys efficiently. Learn more