What is enterprise content management for Life Sciences
Enterprise content management for Life Sciences helps link and seamlessly share documentation to bring safe, high-quality drugs and medical devices to market faster and at a lower cost. Enterprise content management for Life Sciences also unifies processes that extend across domains, divisions and external partners throughout the drug lifecycle.
OpenText Documentum for Life Sciences features
Reuse and share regulated content
Deploy multiple solutions in the same repository, leveraging a shared enterprise information architecture with common, industry standard inventory and data models.
Industry-standard business processes
Leverage comprehensive, predefined document taxonomies, lifecycles and workflows based on industry best practices for pharmaceutical and medical device products to reduce deployment time and ensure adherence to industry standards.
Link content throughout drug lifecycle
Use multiple solution modules in a single repository for cross-domain searches and linking. Users have a single log in to view all the content they are authorized to access based on their role and permissions in one place.
Auditable actions on the go
Role-based user experience for managing information and tasks anywhere, anytime, on any device, whether a laptop, tablet or phone, without compromising security or compliance.
Cloud-native runs anywhere
Deploy on-premises and in any cloud, making it easier than ever to upgrade to the latest version and take advantage of new features, capabilities and updates.
Customer success stories
Benefits of OpenText Documentum for Life Sciences
Single source of regulated content
Eliminate unnecessarily importing and exporting content from one system to another using a common object model and intelligent automation to share and reuse regulated content across the extended Life Sciences organization with clinical, regulatory and quality content and processes.
Predefined, yet flexible business rules enforce corporate document controls, while enhancing local productivity with a solution that unifies document creation, approval, change control and retrieval.
Minimize compliance risk
Reduce noncompliance risk by automating and enforcing appropriate approval processes with automatic assignments. Demonstrate compliance through extensive audit trails, access control, lifecycle management and version control.
Integrate with existing infrastructure, on-premises systems and in any cloud, such as regulatory information management systems, learning management systems and enterprise resource planning systems, that must work together to share complete, accurate and compliant documentation.
Contact us to speak with a member of the Life Sciences team
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