ClinOps VPs, Study Managers, and CRA Managers are often frustrated by missing data and error-prone manual workflows. Saama solves these problems by automating oversight and collaboration across studies, systems, and CROs at every stage.
- Enhance enrollment, compliance, and site productivity efforts
- Save time and achieve milestones with automated alerts, which identify issues early so you can resolve them before they become major problems
- Use an AI-powered virtual assistant to answer thousands of common questions instantly, without having to track down an expert
- Quickly generate reports and deliver context-based insights to stakeholders via email or text
“Great integration of products into existing software to enhance capabilities*”
Through a single operational portal, you can achieve comprehensive, real-time oversight of every study in your portfolio. Because data from your CTMS, EDC, ePRO, IxRS, and other systems is integrated and standardized into a unified study data model, you 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.
Risk Based Quality Management (RBQM)
Saama delivers an end-to-end solution that continuously engages users across the study lifecycle, from design and conduct to evaluation and reporting. With risk assessment plans, anomaly detection, automatic notifications, a collaborative tasking system, and built-in KRIs and QTLs, RBQM sets you up for success in managing and mitigating risk.
Since implementing Saama for its data needs, the Leukemia & Lymphoma Society has realized a cost savings of 10-25%.*
Access Out-of-the-Box Features in 4 Weeks—Guaranteed.
Saama can put you on the fast track to clinical trial process innovation.