QDMS: Quality Document Management System

Content Management for Quality and Beyond

Configurable Indexes, Workflows, Document Types, Required Documents, and Dashboards, TI provides a single place for Content Management. Create rooms to share and collaborate on clinical documentation for trials, Quality Management, Regulatory, Departmental Workspaces, and much more. TI is designed to align document work streams with regulatory compliance practices for document authoring, approval, control, and training.

Author to Archive

Complete the end-to-end process, collaborative document review and authoring, version control, automated approval, and periodic review processes with built-in 21 CFR 11 compliant electronic signatures.

Integrated Process for SOPS and Policies

Review and approval cycles, TI Content Management is completely integrated with Global Learn for procedural document training. Content Management rooms can also be linked to eTMF rooms for seamless sharing of study documentation.