- User-friendly technology
- Reduce study build time
- Capture data from any source
- Run efficient multicenter studies
- Randomize patients with our IWRS module
- World-class support and professional services
- FDA 21 CFR Part 11 compliant
- The best reviewed EDC platform in the world
"High-quality and compliant EDC"
“Our clinical study managers are able to build out each study with little to no help from Castor. The database is easy to use by both clinical sites and sponsors. As an early-stage start up company we are happy to have found a high-quality compliant system we can afford.”
-Lisa Misell, Dyve Biosciences
"Intuitive platform, easy to set up"
“We found Castor EDC very easy to set up on our own and use. We always get an answer straight away when we have questions. It’s a cost-effective alternative to paper CRFs and much safer and easier to use.”
-Petra Jongmans, Atos Medical
"Easy to use, well-designed, and very helpful"
“Castor EDC has been everything we hoped it would be. It is easy to learn and set up. Our study sites have liked it and found it very easy to use. It is feature-complete, doing everything we need it to do.”
-Bill Haack, Cadex Genomics