Purpose-Built for Regulated Life Sciences Content
Docuvera is a structured content authoring platform developed specifically for life sciences. From global labeling and regulatory submissions to SOPs, clinical documents, and medical information, our platform replaces scattered files with modular, traceable, and compliant content components.
With Docuvera, regulated content can be created once and reused across teams, document types, and global markets—helping reduce cycle times, improve consistency, and modernize content operations.
What Sets Docuvera Apart
Built for Pharma
Docuvera isn’t adapted from commercial content tools. It’s designed for the requirements of pharma regulated environments—supporting structured content across labeling, CMC, clinical, safety, pharmacovigilance, and quality functions.
Structured for Compliance
Each content block includes built-in version control, audit history, and metadata—supporting compliance with 21 CFR Part 11, Annex 11, and other applicable standards.
Designed for Reuse
Reusable content components reduce duplicate authoring and review effort—enabling faster updates to CCDS, SmPCs, DSURs, SOPs, and safety documentation.
Validated SaaS
Docuvera is a validation-ready SaaS solution hosted on SOC 2-certified infrastructure. It combines secure architecture with flexibility without adding unnecessary complexity.
What can AI + structured content do for you?
Docuvera combines the automation of AI to deliver efficiency
with the control and governance of structured content
to transform how you do business.
82%
Content Reuse
Reuse approved content components versus rewriting, copy, or 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.
Explore Solutions by Use Case
Docuvera supports documentation processes where precision, compliance, and scale are essential.
Global Labeling
Structured content for CCDS, SmPC, USPI, and ePI—with support for local and global needs.
Chemistry, Manufacturing, & Controls (CMC)
Author or update content once and adapt it across Module 3 and site-specific variations.
Clinical
Standardize protocols, CSRs, and investigator brochures to streamline workflows and reduce rework.
Medical Information
Manage modular scientific response content with traceability across formats and regions.
Pharmacovigilance
Support recurring safety and regulatory reports with version-controlled components.
Quality & SOPs
Replace static SOPs with structured documentation governed by built-in version control.
Why Structured Content Matters Now
Pharma content requirements are expanding: tighter timelines, broader regulatory demands, and evolving submission formats like ePI and eCTD 4.0.
Docuvera enables:
- Faster updates to regulated documentation
- Centralized oversight with the flexibility to support local variation
- Comprehensive audit records for all content types
- Output to eCTD, PDF, XML, and other regulatory formats
- Sustainable improvement in how regulated content is created and maintained
Trusted by Life Sciences Teams Globally
Docuvera works with enterprise and mid-sized companies across the U.S., EU, APAC, and LATAM. Whether you’re starting with structured content or expanding across functions, our platform is designed to support adoption without disruption.
We work with the world’s best
AI + Structured Content
A new era of pharmaceutical documentation
There’s a dynamic duo transforming the face of the pharmaceutical industry. AI technology plus a structured content solution that offers the powerful controls and standardization mandatory for the highly regulated pharmaceutical world.
How our AI + structured content solution works
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.
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.
Efficient, flexible changemanagement
Real-time automatic notifications are sent when reused content changes. Quickly view changes and update local documents appropriately.
Quick and easy publishing tomultiple channels
Create different document types (Word, PDF, HTML, etc.) with different styles from a single project. Automatically upload to existing downstream system.
Robust, detailed reportingand 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.