Saama provides actionable insights for better decision making at the leadership level. With our solutions in place, CEOs, Chief Medical Officers, clinical development executives, and other key stakeholders can increase study quality while maintaining budgets, ensuring compliance, and upholding a stellar corporate reputation.
- Save time and achieve milestones with automated alerts, which identify issues early so you can resolve them before becoming major problems
- Drill down to root cause for faster query resolution
- Use historical data patterns to anticipate outcomes in advance
Saama’s Operations Insights solution delivers a quick, comprehensive overview of risk, quality, and performance indicators across a single study or your entire portfolio, so you can track day-to-day operations and long-term trends.
Because data from your CTMS, EDC, ePRO, IxRS, and other systems is integrated and standardized into a unified study data model, your ClinOps team can quickly identify, visualize, analyze, and address issues early, before they cause major study delays. Automated alerts and task management tools make collaboration more responsive and efficient, and Saama’s AI-powered virtual assistant, known as DaLIA, provides instant answers to thousands of common operational questions.
In order to oversee the development of protocols and documentation for clinical studies, Chief Medical Officers, ClinOps VPs, and other executives need access to comprehensive safety and subject-level data in real time.
Clinical Insights puts all this data in a central repository, so data managers and medical review teams can avoid duplicative efforts, collaborate more effectively, and quickly visualize trends and outliers. Graphical patient profiles and dynamic line listings focus attention on changes to data and automated alerts enable a faster response to data quality issues.
Access Out-of-the-Box Features in 4 Weeks—Guaranteed.
Saama can put you on the fast track to clinical trial process innovation.