Skip to content
Standards we work to: GAMP 5, FDA 21 CFR Part 11, EU Annex 11, ALCOA+ Data Integrity, PIC/S Guidance, ISO 9001:2015, EudraLex Vol 4, Validation Master Plan, Risk-Based · FMEA, CSA · Software Assurance, Audit-Ready Documentation, SDLC

Document Management System

Controlled documents,from draft to master copy.

Create document workflows for review and approval, maintain approved master copies and manage versions across different document types.

What it does

Fit the software to the way you work

The Document Management System keeps regulated documents moving through a defined lifecycle while preserving clear ownership, approval status and version history. It can be configured around the document types and approval steps your quality system already uses.

Core capabilities

Turn controlled processes into visible progress

Approval workflows

Route documents through defined review and approval steps with clear responsibilities and status.

Master-copy control

Store the current approved document as the controlled master copy for reliable use and distribution.

Version management

Maintain versions and history across SOPs, policies, forms and other controlled document types.

Next step

See how Document Management System fits your workflow.

Bring your current process. We will map the fit, identify the right controls and show you the shortest route to a working, validation-ready system.