Evalus AI

Real-World Research. Delivered with Scientific Rigour and Operational Clarity. At Evalus AI, we help pharmaceutical, biotech, and medical device companies run smarter late-phase studies. Whether it's Real-World Evidence (RWE), PMS, registries, or long-term observational trials, our platform makes complex research simpler, faster, and fully compliant. Evalus offers a modular suite of validated tools tailored for late-phase research and real-world settings. Our platform enables sponsors to streamline data collection, ensure regulatory alignment, and reduce operational complexity. Our product includes: • Electronic Data Capture (EDC) • Clinical Trial Management System (CTMS) • Electronic Patient-Reported Outcomes (ePRO) • Electronic Trial Master File (eTMF) • eConsent and Remote Patient Monitoring All modules are built in accordance with 21 CFR Part 11, ICH-GCP, HIPAA, EU-GDPR, and ISO 27001 standards. Our technology-enabled workflows accelerate data capture and improve data quality while keeping study teams inspection-ready at all times. Why Choose Evalus? • Purpose-built for late-phase and RWE studies • Modular, interoperable digital platform • Built by regulatory and scientific experts • Strong compliance foundation • India-based operations, globally scalable execution From protocol design to publication, Evalus brings together regulatory precision, scientific clarity, and operational flexibility, helping our clients turn post-approval data into meaningful, measurable insights.