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Medical device clinical trial platform one-pager
Castor replaces disconnected DM tools and CRO handoffs with one platform and one expert team. Fixed-fee, submission-ready.
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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.
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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.
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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.
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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....
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Castor Catalyst
Castor Catalyst revolutionizes real-world evidence generation by automating data extraction from EHR and claims data. Built with AI-driven...
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Castor On-site ePRO
Download our On-site ePRO factsheet to view an overview of our services.
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Castor eConsent: Streamlined Participant Onboarding for Trials
Download our eConsent factsheet to view an overview of our services.
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Oncology factsheet
Download our oncology factsheet to view an overview of our services.
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Real-world evidence factsheet
Download our RWE factsheet to view an overview of our services.
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eCOA/ePRO factsheet
Download our ePRO/eCOA factsheet to view an overview of our services.
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Try Castor EDC For Yourself

Start designing your own study structure and forms today.

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Try Castor EDC For Yourself

Start designing your own study structure and forms today.

Try For Free