Powering thousands of clinical trials for over 500 customers in 100+ countries, Castor delivers end-to-end success for biopharma, CROs, and medical device companies through expert consultancy and innovative technology.
Our API-first platform is trusted by over 400 sponsors and CROs across more than 2,500 commercial trials to deliver cleaner data, faster. We give your team the power of a modern toolset, backed by expert support when you need it. No black boxes, no hidden fees, no waiting on a vendor’s schedule.
From cutting-edge technology to expert consultancy, Castor empowers biopharma, CROs, and medical device companies to navigate trial complexities, drive efficiency, and deliver results. We’re more than software – we’re your strategic partner in study delivery.
Streamline R&D with integrated solutions for Phase I-IV trials and RWE studies. Cut costs, accelerate development, and ensure seamless data compliance.
Achieve FDA and EU MDR compliance with user-friendly data management. From early-phase studies, to post-market surveillance and PMCF.
Boost operational efficiency with standardized global processes and real-time visibility. Support diverse sponsors across biotech, pharma, and MedTech.
Unlock the full potential of your studies with Castor’s powerful yet intuitive core technologies, seamlessly integrated to deliver exceptional efficiency and data quality across your entire trial.
Capture patient and clinician outcomes seamlessly. Enhances data quality and engagement across decentralized and traditional trials.
Remote digital consent with video calls, multimedia education, and real-time monitoring. Enhances participant diversity and comprehension while reducing site burden.
Comprehensive Clinical Data Management System with data collection, cleaning, and reporting tools. Ensures data integrity and faster insights for regulatory submissions.
Self-driving clinical studies with AI-powered EMR extraction via FHIR/HIPAA APIs. Automates patient screening and chart review with 21 CFR 11 compliance for observational studies.
Expert consultancy and hands-on support for study design, implementation, and optimization. We act as an extension of your team, bringing deep industry knowledge to achieve your research goals.
Expert guidance to translate your protocol into a robust, efficient study database.
On-demand assistance with data cleaning, quality assurance, and reporting.
Technical expertise to connect Castor with your other critical research systems.
Full-service eCOA with multilingual support, scale licensing, and language translations.
We combine innovative solutions that push the boundaries of clinical research with a steadfast commitment to practical, measurable results.
Our integrated platform and Solution Consultant support mean less overhead, faster timelines, higher-quality data, and exceptional compliance for your trials, whether you’re a biopharma innovator, a global CRO, or a focused medical device company.
Are you ready to transform your clinical trials? Connect with a solutions consultant today.
Castor’s platform enforces strict data validation rules, customizable at the field level, to prevent errors at the point of entry. Our system includes real-time query management, source data verification tools, and comprehensive audit trails, ensuring data accuracy and reliability from collection through analysis. This proactive approach minimizes discrepancies and streamlines the data cleaning process.
Castor offers a robust, well-documented API designed for flexible, bi-directional integration with various third-party systems, including CTMS, central labs, and pharmacovigilance platforms. Our integration strategy focuses on automated data exchange to reduce manual effort and ensure data consistency across your entire research ecosystem. We also provide professional services to support complex enterprise-level integrations.
Castor’s intuitive, drag-and-drop study builder allows for rapid configuration of new studies, often within weeks for complex designs. The platform is built for agility, enabling efficient mid-study protocol amendments without disrupting ongoing data collection. Our aim is to empower your team with tools for quick adaptation and minimal reliance on external support for routine changes.
Yes, Castor’s software adheres to stringent global regulations, including FDA 21 CFR Part 11, GDPR, and HIPAA. We provide a comprehensive, immutable audit trail for every data point and action, meticulously recording user, timestamp, and changes. This audit log is easily accessible and exportable in a transparent, inspection-ready format, ensuring full compliance for international regulatory bodies.
Download our RWE factsheet to view an overview of our services.
Download our ePRO/eCOA factsheet to view an overview of our services.
Discover how Oncobiomix used an integrated platform for eConsent, EDC, and ePRO to save $100K and streamline data capture.
eConsent regulations can vary widely across borders. Download this whitepaper to learn 24 countries’ stances on the use of eConsent.