Manage and oversee your clinical trials in real time
How Agatha helps you
Centralize your clinical operations
Bring together all information related to your studies, sites, investigators, patients, and vendors in a single environment to simplify day-to-day management and eliminate information silos.
Monitor your studies in real time
Instantly access key metrics, protocol milestones, site performance, and patient enrollment progress to quickly identify risks and potential delays.
Ensure traceability and compliance
Maintain a complete history of activities, monitoring visits, deviations, and corrective actions to meet regulatory requirements and support inspection readiness.
Connect your clinical processes
Agatha CTMS integrates natively with Agatha eTMF and eISF, ensuring seamless operational and document continuity throughout your clinical trials.
Solution benefits
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Accelerate study start-upCentralize critical study information from day one and simplify the management of sites, teams, and vendors. -
Gain complete visibility into your clinical trialsTrack study progress, site performance, and operational KPIs in real time through configurable dashboards. -
Strengthen operational oversightManage monitoring visits, deviations, corrective actions, and follow-up activities from a single platform. -
Reduce risks and delaysIdentify operational issues, enrollment challenges, and vendor-related risks early so you can take action before they impact your timelines. -
Improve quality and complianceEnsure complete traceability of study activities while maintaining documentation that is always up to date and inspection-ready. -
Drive user adoptionProvide your teams with an intuitive solution designed specifically for clinical operations and easy to deploy across your organization.
Agatha CTMS Features
Centralized study management
Centralize study data, manage protocol versions, track study status, and monitor key milestones throughout the clinical trial lifecycle.
Site management
Consolidate site information, monitor site activation and performance, and maintain complete oversight of site activities.
Team and stakeholder management
Manage CRAs, investigators, study coordinators, and other stakeholders, define roles and responsibilities, and track assignments.
Vendor and partner management
Manage CROs, laboratories, and external service providers, centralize contracts, and monitor vendor performance. Associated documents are automatically archived in the eTMF.
Ready do dive in?
For inquiries about our products and services, or to sign up for a demo, click here.