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
Site Regulatory Documents
Study-related Forms
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