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Risk Based Monitoring

With a risk-based management approach, you have a better chance at ensuring site productivity and responding to site-specifc issues before they become major problems. Combining statistical data checks, automated alerting, and other RBM techniques with site visits and traditional data verification gives you a powerful quality control solution.

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Use Cases/Value Drivers

Portfolio & Study Oversight
With real-time access to all your study data, automated alerts, and a revolutionary Deep Learning Intelligent Assistant (DaLIA) that lets you query your data for immediate answers, Risk Based Monitoring gives you everything you need to track performance and ensure that milestones are met.
Risk Assessment & Categorization
Real-time dashboards identify issues within specific risk areas, utilizing visual indicators. Thresholds and weights can be adjusted to see how specific changes affect overall outcomes.
Automated Threshold Breach Detection & Alerting
This predictive approach identifies issues earlier, so corrective action can be taken before it’s too late.
Centralized Monitoring
The ability to evaluate study data remotely conserves valuable resources by eliminating the majority of physical site visits you have to make.
Task & Workflow Management
Collaboration tools track decisions, actions, and outcomes in a fully auditable way.

Access Out-of-the-Box Features in 4 Weeks—Guaranteed.

Saama can put you on the fast track to clinical trial process innovation.

Terms & Conditions

By inquiring about Saama’s Database Lock in a Day, you agree to be contacted by Saama and to allow Saama to use, maintain, store, and protect your personal data in accordance with our Privacy Policy.

Eligibility details are for informational purposes only. Saama, in its sole discretion, will determine your eligibility based on the information you disclose as part of the intake process. If Saama determines that you are eligible to participate, you will be notified by separate email. Eligibility depends on certain criteria, such as the size of your company, the types of clinical trials you sponsor, and the number of patients in–and stages of–your current clinical trials.

By completing the request form, you represent that you have authority to proceed on behalf of your company. Should you agree to participate, you agree to reasonably cooperate with Saama in following the guidelines and procedures required for integrating, standardizing, and analyzing your data. Participation requires the use of our Smart Data Quality application, a technology-agnostic AI engine that sits on top of your current infrastructure. The application can be used immediately, and you’re only charged for the services you use based on a predetermined estimate.

Information you share with Saama during your participation may be anonymized and/or aggregated, and made available publicly in Saama marketing materials. This information may include: types of systems and processes involved, types of departments involved, and size and regional location of your company. Such information will never be directly associated with you, nor will you or your company be identifiable without express written permission.