Castor provides a cloud-based clinical data platform that integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) to facilitate decentralized clinical trials. This platform enables researchers to efficiently collect, manage, and analyze data from multiple sources while ensuring compliance with regulatory standards, ultimately reducing the time and complexity of clinical trial processes.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical trials often face challenges in efficiently capturing, managing, and integrating data from various sources, including electronic health records, patient-reported outcomes, and wearable devices. Traditional methods can be time-consuming, costly, and prone to errors, hindering the progress of research and development. Ensuring compliance with regulatory standards such as GDPR, HIPAA, and 21 CFR Part 11 adds further complexity.
Solution
Castor provides a unified, cloud-based eClinical platform designed to streamline data capture and management for clinical trials. The platform integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) modules to facilitate efficient data collection from multiple sources. By centralizing data management, Castor enables researchers to monitor study progress in real-time, improve data quality, and accelerate trial timelines. The platform's self-service capabilities and user-friendly interface empower researchers to build and deploy studies with minimal support, while ensuring data security and regulatory compliance.
Target Audience
The primary target audience includes researchers in biotech and pharmaceutical companies, medical device and diagnostics firms, contract research organizations (CROs), and academic institutions involved in clinical trials and real-world evidence studies.
Features
- Integrated EDC, ePRO, and eConsent modules for comprehensive data capture
- Compliant with 21 CFR Part 11, ICH e6 GCP, GDPR, and HIPAA regulations
- Real-time reporting and monitoring of study health and progress
- Secure data storage with ISO27001 and ISO9001 certifications
- Patient-facing technology to remotely recruit, screen, and enroll patients
- Integration capabilities with various data sources and vendors
- Self-service platform for easy study building and deployment
- Electronic data capture (EDC) system to maximize productivity by capturing, processing, and integrating data from multiple sources and vendors