Clinical Trial Management System (CTMS)
Harmonize clinical trial management with every facet of the research process
Efficiently manage your regulatory workflow by collecting, accessing, and connecting all your site documentation and study data in a single, centralized location. On the TrialKit platform, CTMS and EDC truly work in unison to enhance productivity and collaboration for research teams.
Securely track and manage study activities
The highly configurable role-based access and permissions in TrialKit CTMS make it easy for research teams to perform tasks in a regulatory compliant, secure manner. Robust reporting and analytics capabilities allow you to closely follow study progress and performance, ensuring important milestones are met at every level.
Study Documents/File Management
- Manage documents via a centralized study document manager
- Upload documents to any CRF
- Access documents via the document viewer
- Annotate documents by user
- Redact documents by user
Site Regulatory Documents
- Manage documents via a centralized site regulatory document manager
- Define site enrollments based on site document completion rules
- Create forms to assign and track regulatory documents by site
- Link enrollment to regulatory document completion
- Show site-based status of regulatory document completion
Study-related Forms
- Capture study-related data such as the protocol or study materials/inventory
- Build and deploy study-related forms such as protocol approvals, financial disclosures, delegation of authority, regulatory log, and site essential docs to the web
