Clinical Insights

Medical monitoring is essential to ensuring patient safety and proving the efficacy of treatments under study during clinical trials. The integration of patient safety and subject-level data from your EDC, ePRO, labs, and other systems is driven by the Study Data Tabulation Model (SDTM) standards from the Clinical Data Interchange Standards Consortium (CDISC). Saama enhances your analytics capabilities for more accurate review and more informed decision-making. What’s more, Saama’s revolutionary Deep Learning Intelligent Assistant (DaLIA), lets you query your data for immediate answers to thousands of common questions, without having to wait for access to subject matter experts at your company.

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Use Cases/Value Drivers

Holistic Patient Data Review
Graphical patient profiles, which include multiple time-series charts in one location, provide a holistic view of every patient. Lab value averages—by cohort and visit—provide insights into subject trends.
Data Review Tracking
Dynamic line listings highlight new and changed data, to simplify the medical review process.
Data Reconciliation
When your entire medical review process is automated, you can easily highlight discrepancies, handle exceptions, and create and manage auditable tasks for items needing additional investigation.
Safety & Efficacy Signal Analysis
Issues related to adverse events and protocol deviations are easily identified and categorized for faster resolution.
Clinical Data Standardization
Data from disparate sources is aggregated into a Unified Study Data Model, which makes it easy to analyze events and create and distribute meaningful reports.

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

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