Castor Solutions

1. A Clinical Data Platform For First-In-Human To Post-Market 10/14/2026

   Running a device study with a small team? See how one platform handles data capture, consent, and long-term follow-up from first-in-human to post-market.

2. High-Quality, ALCOA+ Device Data Under EU MDR And ISO 14155, Without Building A Data Management Team 10/14/2026

   Lean device team? Learn how expert data management and human-reviewed AI help you deliver high-quality clinical evidence for stronger regulatory submissions.

3. Run Your EU MDR PMCF Program On One Platform 10/14/2026

   Running EU MDR PMCF for years? Now it all fits on one platform: find patients, re-consent remotely, pull charts with AI, and automate follow-up.

4. ICH E6(R3) Is Here: How Should You Handle It? 5/27/2026

   Prepare for ICH E6(R3) with integrated oversight, audit-ready data, and streamlined trial operations designed to reduce burden, accelerate timelines, and support compliance.

5. Data Management Without The Coordination Friction 5/27/2026

   Simplify clinical data management with one connected platform and an expert team delivering faster study startup, cleaner data, fixed-fee predictability, and fewer operational delays.

6. Expand Your Range Of Data Capture 3/31/2026

   Capture patient data with total flexibility. Administer surveys on any device, switch mid-questionnaire without losing progress, and eliminate the need for specialized hardware or extra apps.

7. Castor Professional Services: Your Trial Delivery Partner 3/17/2026

   Accelerate clinical trial timelines and ensure audit-readiness with expert-led build models, AI-driven data management, and global participant support designed to streamline your path to submission.

8. Benefit For An AI-Automated Extraction Model 3/9/2026

   Modernize your research by replacing manual data entry with automated extraction. Ensure regulatory-grade evidence and full data traceability for faster, more reliable results.

9. Generate Regulatory-Grade, RWE With Speed And Efficiency 11/21/2025

   For teams managing real-world evidence or post-market studies, automation offers a scalable solution to streamline workflows, maintain compliance, and accelerate decision-making.

10. Castor-eCOA Clinical Trial Technology 8/21/2025

    1,735 eCOA & ePRO Studies Completed 

    eCOA and ePRO with Enrollment, eConsent, Payments and EDC integrated. Our services cover build, licensing and 24/7 support.

    95%+ Patient Compliance Rate

    4-8 Weeks to Deploy

    190+ Validated Instruments