Data management without the coordination friction
Castor replaces disconnected DM tools and CRO handoffs with one platform and one expert team. Fixed-fee, submission-ready.
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Biotech clinical trial data management
Castor delivers expert data management for biotech trials. Submission-ready from day one. No intermediary layers.
ICH E6(R3) compliance for biotech studies
See how Castor's unified platform helps biotech sponsors meet ICH E6(R3) oversight, data integrity, and site burden requirements.
ePRO for biotech: capture economic evidence from day one
Castor ePRO helps biotech sponsors capture HEOR-ready evidence from Phase I/II. Audit-proof, 92%+ participant compliance.
Castor Professional Services: Expert Clinical Study Builds
Castor’s Professional Services team offers end-to-end support for clinical trial implementation, including EDC build, eCOA, and data management....
Castor Catalyst
Castor Catalyst revolutionizes real-world evidence generation by automating data extraction from EHR and claims data. Built with AI-driven...
Castor On-site ePRO
Download our On-site ePRO factsheet to view an overview of our services.
Castor eConsent: Streamlined Participant Onboarding for Trials
Download our eConsent factsheet to view an overview of our services.
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.
eCOA/ePRO factsheet
Download our ePRO/eCOA factsheet to view an overview of our services.