Manage the large volumes of patient data collected during clinical trials with a streamlined system that delivers features for modeling any kind of clinical study, automatically storing components for reuse in a flexible global library.
Boost productivity with a full-featured interface that lets investigators, monitors, and site coordinators enter and clean clinical data, monitor trial progress, and track source-document verification
Readily manage more than 100 dictionaries and handle the complexities of the Medical Dictionary for Regulatory Activities (MedDRA), including the multi-axial hierarchy of a dictionary
Store and monitor all adverse events information so that safety concerns can be addressed before a drug reaches the market
Accurately capture and manage study data within a single platform and expedite analysis with dynamic, real-time displays
Carefully and actively manage clinical trials by maintaining contact with sites, monitoring and resolving issues, and scheduling site visits based on investigator availability, site enrollment, or completed work
Drive business process consistency based on regulatory mandates and your organization's standard operation procedures using flexible, pre nonbuilt visit report templates