Marvin EDC is a secure, cloud-based Electronic Data Capture software designed to manage clinical trial data, particularly for complex and oncology studies. It facilitates AI-powered study setup, data collection, and monitoring, supporting FDA/EMA compliance. Key features include RBM (Risk-Based Monitoring), ePRO, eConsent and randomized trial management. Key Aspects of Marvin EDC Core Functionality: It enables secure, browser-based data entry (including double data entry), data validation, and real-time monitoring of clinical trial sites. Targeted Use Cases: Highly suited for complex, oncology, and academic trials due to its flexibility in handling complex workflows. Integrated Platform: Beyond basic EDC, the suite includes coding, randomization (IWRS/RTSM), ePRO (patient reporting), and eConsent. Compliance & Data Quality: The system is CDISC ODM-certified and complies with 21 CFR Part 11 and ICH-GCP standards. Development: Developed in Germany (by AB Cube Germany), it has supported over 1,500 studies worldwide since 2002. It is widely used by researchers to ensure accurate data capture and streamline the data management process.