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.
- Optimize enrollment, compliance, and site productivity
- Automate oversight and collaboration across studies, systems, and CROs
- Enable automatic alerts when predetermined thresholds are breached
- Allows you to dynamically converse with your data through an AI-powered virtual assistant.
- Push context-based insights to stakeholders via email or text
Track the status of each study in real time and proactively identify issues that could cause milestone delays.
- Integrate and harmonize data from your 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
- Answer questions instantly through an advanced, AI-powered virtual assistant
- Use historical data patterns to predict future outcomes
- Provide CRO oversight consistent with good clinical practice, as outlined in ICH E6(R2) guidelines
- Easily generate tabular and visual reports for presentations and internal review
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.