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.
- Increases visibility by removing data silos
- Provides transparency and drives collaboration
- Fully configurable to optimize processes
- Generates site visit documents
- Easy monitoring of study progress and performance
- Investigator database with site creation and contact management
- Site visit scheduling and management
- On-site/remote monitoring visit documentation with eSignature and eTMF integration
- Protocol deviation, action item, and communication log management
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.