A unified reporting hub that delivers real-time, study-wide insights across sites, subjects, inventory, shipments, data management, medical coding, CRFs, and more.
Explore our documentation or contact our support team for questions about our solutions.
Our Reporting module offers a robust and comprehensive framework with the following core features:
Export reports into Excel and PDF formats.
All study-specific reports include Study Name, Description, Report Name, Generator, and Timestamp.
High-performance report generation for large studies.
Accurate, validated data aligned with clinical, IRT, EDC, and CTMS workflows.
An extensive suite of reports grouped across operational, clinical, supply, compliance, and subject-level activities.
The Reports Module is one of the most comprehensive reporting ecosystems in the clinical trial technology landscape. It provides full transparency, multi-level auditability, real-time insights, and regulatory-grade reporting for every stakeholder.