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, lab, and subject-level data together for consistent and proactive medical review. Innovative capabilities let you work at a higher level, to maximize patient safety and prevent delays. Integrating EDC, Lab, ECG, ePRO, IxRS, and other data into a unified study data model makes it possible to customize KPIs and analytics, visualize trends and identify outliers in real time, and 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.