AI TOOL PROFILE
Castor EDC: eClinical Data Management Software
- Healthcare
- Data Management
- Pharmaceutical companies
- Biotech firms
- Contract Research Organizations (CROs)
- Medical device and diagnostics companies
- Academic researchers
Pricing
Castor uses subscription-based, quote-based pricing tailored to study complexity and duration. A free trial is available for the core EDC tool.
At a glance
- Best for
- Pharmaceutical companies, Biotech firms, Contract Research Organizations (CROs), Medical device and diagnostics companies, Academic researchers
- Key use cases
- Clinical Trial Data Capture, Remote Patient Enrollment, Real-World Evidence (RWE) Generation, Post-Market Clinical Follow-up
- Integrations
- EMR/EHR via HL7 FHIR, RESTful API
- Official website
- Visit castor edc official website
How AI is used
Castor is a cloud-native eClinical platform designed to support the lifecycle of clinical trials. It provides a unified environment for Electronic Data Capture (EDC), patient-reported outcomes, and digital consent, which may help research teams reduce manual data transcription between different systems.
The tool is designed for a variety of research organizations, including academic institutions, pharmaceutical companies, and Contract Research Organizations (CROs). It supports both traditional and decentralized clinical trial (DCT) workflows, allowing for remote patient recruitment and screening.
Buyers can use the platform's AI capabilities via Catalyst to help automate tasks such as EMR data extraction; these actions require human-in-the-loop oversight to maintain regulatory compliance. The platform is designed to meet global standards including 21 CFR Part 11, GDPR, and HIPAA.
Before choosing this tool, buyers should confirm how the quote-based pricing aligns with their specific study complexity and duration, and verify that the regional data residency options meet their local legal requirements.
Key Features
Electronic Data Capture (EDC)
A system for collecting and managing clinical trial data with a no-code eCRF builder for study setup.
eCOA and ePRO
Tools for capturing patient and clinician-reported outcomes within the platform to help avoid data reconciliation.
eConsent Management
Digital informed consent solutions including multimedia education and remote video conferencing.
Catalyst AI
An AI engine that helps automate EMR data extraction and patient screening with mandatory human sign-off.
Decentralized Trial (DCT) Solutions
Features designed to support hybrid and remote trials, including BYOD (Bring Your Own Device) support.
Compliance Framework
Support for 21 CFR Part 11, ICH GCP, GDPR, and HIPAA, with an immutable audit trail.
Use Cases
Clinical Trial Data Capture
Using the EDC and eCRF builder to collect and clean research data for regulatory submissions.
Remote Patient Enrollment
Managing the digital informed consent process and remote screening for decentralized studies.
Real-World Evidence (RWE) Generation
Automating the extraction of variables from unstructured source documents like EMRs and PDFs.
Post-Market Clinical Follow-up
Supporting medical device companies with EU MDR and FDA compliance for post-market surveillance.
Integrations
- EMR/EHR via HL7 FHIR
- RESTful API
FAQ
How does Castor handle regulatory compliance?
- Castor is designed to comply with FDA 21 CFR Part 11, GDPR, HIPAA, and ICH GCP, and it maintains ISO 27001 and 9001 certifications.
What is the 'Self-Driving Study' feature?
- This refers to workflows using the Catalyst AI engine to help automate tasks like EMR extraction and screening, though all actions require human-in-the-loop sign-off.
How is Castor priced?
- Pricing is subscription-based and customized via quotes depending on study complexity, duration, and the specific modules required.
Source category: Healthcare
Source subcategory: Data Management
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