ClinOps VPs, Study Managers, CRA Managers—and sponsors—are often frustrated by missing data and error-prone manual workflows. Saama solves these problems by automating oversight and collaboration across studies and systems at every stage.
- Highlight enrollment issues and funnel leakage
- Identify site-level performance issues that might introduce risk
- Compare study performance across sponsors
- Improve CRA productivity and performance
Track the status of your clients’ studies in real time and proactively identify issues that could cause milestone delays.
- Integrate and harmonize data from CTMS, EDC, ePRO, IxRS, and other data systems into a unified study data model
- Quickly identify and address issues to optimize study start-up, enrollment, and compliance
- Allows you to dynamically converse with your data through an AI-powered virtual assistant
- Use historical data patterns to predict future outcomes
Risk Based Monitoring
Go beyond traditional site operations with a centralized database that lowers costs and saves time.
- Reduce compliance and regulatory risk through early notification of site issues
- Allocate site visitation resources more effectively
- Use custom KRIs and root-cause analysis to identify and address issues more quickly
Access Out-of-the-Box Features in 4 Weeks—Guaranteed.
Saama can put you on the fast track to clinical trial process innovation.