## Castor Resources

### Categories

### Topics

- [All Topics](/content/resources/factsheets/index.html)
- [AI](/content/resources/factsheets/?topic=ai/index.html)
- [biotech](/content/resources/factsheets/?topic=biotech/index.html)
- [Data Management](/content/resources/factsheets/?topic=data-management/index.html)
- [eCOA](/content/resources/factsheets/?topic=ecoa/index.html)
- [eConsent](/content/resources/factsheets/?topic=econsent/index.html)
- [EDC](/content/resources/factsheets/?topic=edc/index.html)
- [ePRO](/content/resources/factsheets/?topic=epro/index.html)
- [Oncology](/content/resources/factsheets/?topic=oncology/index.html)
- [Patient-Centric Technology](/content/resources/factsheets/?topic=patient-centric-technology/index.html)
- [Real-World Evidence (RWE)](/content/resources/factsheets/?topic=real-world-evidence-rwe/index.html)

### Factsheets

**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.  
[Learn more](/content/factsheets/medical-device-platform-factsheet/index.html)

**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.  
[Learn more](/content/factsheets/clinical-trial-data-management/index.html)

**Biotech clinical trial data management**  
Castor delivers expert data management for biotech trials. Submission-ready from day one. No intermediary layers.  
[Learn more](/content/factsheets/biotech-clinical-trial-data-management/index.html)

**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.  
[Learn more](/content/factsheets/ich-e6r3-biotech-compliance/index.html)

**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.  
[Learn more](/content/factsheets/biotech-epro-clinical-trials/index.html)

**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....  
[Learn more](/content/factsheets/castor-professional-services-expert-clinical-study-builds/index.html)

**Castor Catalyst**  
Castor Catalyst revolutionizes real-world evidence generation by automating data extraction from EHR and claims data. Built with AI-driven...  
[Learn more](/content/factsheets/catalyst-ai/index.html)

**Castor On-site ePRO**  
Download our On-site ePRO factsheet to view an overview of our services.  
[Learn more](/content/factsheets/onsite-epro-factsheet/index.html)

**Castor eConsent: Streamlined Participant Onboarding for Trials**  
Download our eConsent factsheet to view an overview of our services.  
[Learn more](/content/factsheets/econsent-factsheet/index.html)

**Oncology factsheet**  
Download our oncology factsheet to view an overview of our services.  
[Learn more](/content/factsheets/oncology/index.html)

**Real-world evidence factsheet**  
Download our RWE factsheet to view an overview of our services.  
[Learn more](/content/factsheets/real-world-evidence/index.html)

**eCOA/ePRO factsheet**  
Download our ePRO/eCOA factsheet to view an overview of our services.  
[Learn more](/content/factsheets/epro-ecoa/index.html)

## Try Castor EDC For Yourself

Start designing your own study structure and forms today.

[Try For Free](https://data.castoredc.com/register)

## Try Castor EDC For Yourself

Start designing your own study structure and forms today.

[Try For Free](https://data.castoredc.com/register)