Content Authoring for Life Sciences

Author, review and update once - reuse across multiple documents

Structured component authoring designed specifically for Life Sciences. Improves the efficiency of document creation, review and revisions, while reducing the time spent on every project.

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What is Docuvera?

Docuvera is the most efficient way to create, review and publish Life Sciences documentation.

Docuvera is a single platform to author, review, approve, translate, and publish regulated documents by reusing approved, compliant component content. We solve one of biopharma’s major challenges – the inefficiency of creating and updating documentation through the drug development lifecycle.

What is Docuvera?

Docuvera is the most efficient way to create, review and publish Life Sciences documentation.

Docuvera is a single platform to author, review, approve, translate, and publish regulated documents by reusing approved, compliant component content. We solve one of biopharma’s major challenges – the inefficiency of creating and updating documentation through the drug development lifecycle.

We work with the world’s best

How it works

What can it do for you?

Docuvera will transform how you do business.

When implemented effectively, Docuvera will slash the time needed to create documentation, dramatically increasing output without having to add staff members – making a major improvement to the bottom line.

Typical Docuvera customers see dramatic efficiency and productivity results:

82%

Content Reuse

Reuse approved content components versus rewriting or copy/pasting content

110%

Productivity Gains

Content reuse drives efficiency in creating, reviewing and updating documents

145%

ROI Achieved

Gains in efficiency allows existing teams to do more without having to add headcount

Demonstrated success

Eli Lilly led organizational change to realize successful component authoring with Docuvera

Achieving 65% reuse of components in Global Medical Information in the first year, Eli Lilly Global Medical Information has successfully made the paradigm shift from traditional authoring to component authoring. Hear the four important milestones in Lilly’s adaptive content creation journey and how they applied the 5W framework as a guide to help lead organizational change to component authoring.

Remove the pain of cut and paste

Authors can collaborate simultaneously on documents by easily reusing approved blocks of content to assemble documents. No technical expertise or expensive support required.

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Collaborative review and approval process

Cross-department review of documents can happen collaboratively in a single forum for discussions and resolutions. No more manual merging of Word track changes.

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Efficient, flexible change
management

Real-time automatic notifications are sent when reused content changes. Quickly view changes and update local documents appropriately.

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Quick and easy publishing to
multiple channels

Create different document types (Word, PDF, HTML, etc.) with different styles from a single project. Automatically upload to existing downstream system.

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Robust, detailed reporting
and audit trail

All content updates, reviews, approval workflows and publishing events are captured and stored in the Docuvera audit trail. Document reasons for changes and content deviations as part of the change management process.

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