Every action, every user, fully logged
Patholytix captures a complete, time-stamped record of activity across the IMS, with event logs tied to individual users and study data. Audit trails are continuous and immutable, giving research teams and regulators the visibility needed to demonstrate data integrity at any point in the workflow.
Controlled from access through archive
Patholytix maintains end-to-end chain of custody across the pathology workflow, from controlled access and scoring through to locking and long-term retention. Every step is governed, logged, and reproducible, supporting both GLP submission requirements and GCP trial endpoints within the same environment.
The right data, to the right people, at the right time
Access to studies, slides, and findings is controlled through configurable roles, permissions, and SSO integration. Teams, partners, and external reviewers operate inside the same IMS with visibility scoped to their responsibilities, removing the data-sharing workarounds that erode governance in fragmented systems.
Built to fit your regulatory and IT strategy
Patholytix is available as SaaS, private cloud, or on-premise, with deployment models designed to meet the security, residency, and validation requirements of regulated research. Customers choose the model that fits their IT and compliance strategy without compromising on platform capability or governance.
