Proving efficacy and ensuring patient safety leaves little room for error among medical review teams. Saama removes the lag time between data requests and availability by eliminating manual work, removing data management complexity, and using machine learning to predict outcomes.
- Eliminate manual work through automatic data change highlighting
- Gather the patient-level insights you want via custom configuration
- Gain a fuller picture of your cohorts through the ability to visualize trends, identify outliers, and access actual test results
- Quickly resolve adverse events through early identification at the study, country, site, and patient level
See all your safety and subject-level data together for consistent and proactive medical review. Innovative capabilities let medical review teams work at a higher level, to ensure patient safety and prevent trials from being pushed off course.
- Access clean harmonized data from disparate sources —EDC, Labs, ECG, ePRO, IxRS, etc.—through a unified study data model
- Customize KPIs and analytics for more relevant monitoring in real time
- Set alerts to identify issues sooner for faster action
- View data changes in real time, using dynamic line listings and graphical patient profiles
- Use detailed labs, with access to actual test results, to visualize trends and identify outliers
- Quickly share relevant information using custom dashboards and reports
Access Out-of-the-Box Features in 4 Weeks—Guaranteed.
Saama can put you on the fast track to clinical trial process innovation.