Overview

OpenText™ Documentum™ Content Management (CM) for Life Sciences is a set of comprehensive, purpose-built solutions to transform how organizations access, manage and share regulated content. Leveraging agency guidance and industry leading practices, OpenText Documentum CM for Life Sciences breaks down information silos, reducing complexity while unifying and streamlining processes.

How OpenText Documentum CM for Life Sciences can benefit business

Adapt with cloud-native software

Leverage a containerized architecture to easily upgrade and get access to new features, capabilities and updates, whether on-premises, in a hybrid environment or in the cloud.

Deploy a single source of regulated content

Use multiple solution modules in a single repository for cross-domain searches and linking, eliminating unnecessary importing and exporting between systems.

Reduce noncompliance risk

Demonstrate FDA 21 CFR Part 11 compliance with audit trails, lifecycle management, access and version control and enforce approval processes with automatic assignments.

Boost productivity

Leverage industry-standard business processes for document taxonomies, lifecycles and workflows for pharmaceuticals and medical devices that enforce corporate document controls while enhancing local productivity.

Foster compliant, secure collaboration

Collaborate and reuse content and processes with internal and remote employees, authorized partners and other third parties without compromising security or compliance.

Simplify integration

Integrate with existing infrastructure, on-premises systems and in any cloud, including quality management, learning management and enterprise resource planning systems.