OpenText™ Documentum™ for Research and Development helps organizations efficiently manage regulatory submission documentation creation, review and approval to streamline the submission process. With Documentum for Research and Development, organizations gain complete control of content with uncompromised compliance and secure information sharing across the extended Life Sciences enterprise.
Run anywhere with cloud-native software that offers the choice to deploy on-premises, in a hybrid environment or in the cloud.
Eliminate the need to import and export across systems with one enterprise-wide content source that includes multiple solution modules for cross-domain searches and linking.
Leverage containerized architecture to easily upgrade and access new features, capabilities and updates.
Discover the advantages of using Documentum for Research and Development.Read the overview
Quickly create and advance content to a submission-ready state with predefined yet flexible business rules.
Leverage content security, access controls and automatic versioning to collaborate with employees and authorized partners without compromising security or compliance.
Centralize corporate document control and visibility while maintaining flexibility in workflows and document lifecycles to enhance local productivity.
Demonstrate compliance with access and version controls, detailed audit trails, e-approvals and e-signatures to mitigate risks.
Makes it easy to create submission-ready documentation with approved, compliant templates, locate information using faceted navigation and jumpstart authoring with predefined inheritance rules to re-use content and metadata.
Allows contributors to view a consolidated list of previous edits while simultaneously making changes using workflows or SharePoint, and automatically merges edits to review, accept or reject the changes.
Provides document taxonomies, lifecycles and workflows based on extended DIA EDM reference model for pharmaceutical and medical devices that enforce corporate document controls.
Links and shares content from clinical, regulatory and quality domains automatically so users can plan, create and locate submission-ready content over the full product lifecycle from development to commercialization.
Protects product information with restricted access based on confidentiality needs, using metadata to grant appropriate access to content across the entire product line.
OpenText offers deployment choice and flexibility for Documentum for Research and Development.
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