Configurable Role-Based CTMS
Enhance productivity and collaboration for research teams by efficiently managing regulatory workflows. Organize all site documentation and study data in one centralized location. Use robust reporting and analytics tools to help you ensure important milestones are met.
- Provides transparency and drives collaboration
- Increases visibility by removing data silos
- Automates administrative tasks
- Makes compliance easier through integration with eTMF
- Fully configurable to optimize processes
- Easily monitors study progress and performance
- Generates site visit documents
- Fully configurable
- Protocol deviations, action and communication logs
- Template-driven site visit reports
- Site visit management, scheduling and forecasting
- Site Visit Report documents
- Study and site management
- Contract management
- Investigator database
- Compliance with regulatory standards
- Trial status visibility
- Governance and oversight
- Study performance and metrics reporting
- Issue management
- Supports electronic signatures
- My Page App
CTMS + Study Start-Up
Eliminate communication gaps and missed triggers between start-up and clinical groups. No more relying on email and spreadsheets for crucial site qualification visits and site initiation visits.
CTMS + RBQM
Easily execute on-site, remote, and centralized monitoring visits in a single intuitive platform with consistent and complete reporting.
CTMS + Study Start-Up + RBQM
Take your clinical trial to the next level by adding RBQM. Now, you can effectively manage your study data from the first site identification to the last patient visit.