Centrellis is a clinical trial management software designed to optimize the planning, execution, and monitoring of clinical trials. This platform is used by pharmaceutical companies, research organizations, and healthcare providers to ensure the efficient management of trials and patient data. Centrellis streamlines the entire trial process, from protocol design and recruitment to data collection and analysis. The software features powerful tools for patient enrollment, scheduling, and monitoring, allowing clinical teams to keep track of study progress in real time. Centrellis also supports regulatory compliance by automating documentation management and ensuring adherence to standards such as GxP (Good Clinical Practice) and 21 CFR Part 11. With integrated reporting tools, users can generate trial progress reports, track adverse events, and monitor key performance indicators (KPIs). The platform’s analytics capabilities help organizations identify trends, optimize trial performance, and reduce costs. Centrellis provides a comprehensive solution for managing complex clinical trials, ensuring efficiency, accuracy, and compliance.
Sema4
2017
United States
Proprietary
Clinical Study Management
