Built for the Future of Pharma.

Accelerated Compliance, Efficiency, and Time to Market. At Scale.

Accelerate digital transformation in life sciences with Docuvera’s AI-powered structured content platform. Improve efficiency, reuse, and compliance across labeling, CMC, clinical, medical, pharmacovigilance, and quality documentation.

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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.

THE INDUSTRY’S ONLY GOVERNANCE-FIRST PLATFORM BUILT SPECIFICALLY FOR PHARMA

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 Type 2-certified infrastructure and certified ISO 27001. It combines secure architecture with flexibility without adding unnecessary complexity.

Explore Solutions by Use Case

Docuvera is the only governance-first structured content platform purpose-built for the pharmaceutical industry.

We replace outdated, document-centric systems and siloed tools with a centralized, modular (component) content platform that enables global pharma teams—across Labeling, Clinical, CMC, Medical Affairs, and Pharmacovigilance—to work from a single source of truth.

With Docuvera, organizations eliminate manual rework, ensure regulatory-grade quality, and unlock over 80% reuse of content—accelerating submissions and dramatically improving time to market.

As regulatory requirements grow more complex and AI adoption rises, pharma companies need systems that enable both control and agility. Docuvera delivers the governance, structured data, and AI-readiness required for true digital transformation in regulated global markets.

Global Labeling

Structured content for CCDS, SmPC, USPI, and ePI—with support for local and global needs.

Clinical

Standardize protocols, CSRs, and investigator brochures to streamline workflows and reduce rework.

Chemistry, Manufacturing, & Controls (CMC)

Author or update content once and adapt it across Module 3 and site-specific variations.

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

We Have you covered Prefix

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.

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Get Started

Structured content isn’t a future-state ambition—it’s foundational to digital transformation, and, it’s something pharma companies can use right now to improve quality, oversight, and efficiency. Learn how Docuvera can help you prepare for the future.

Discover how work with the world’s best

A new era of pharmaceutical documentation

AI + Structured Content

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.

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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.

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Modern, high-quality content without the hassles

Harnessing AI, Docuvera’s component authoring and management is the most efficient way to create, review, and publish life sciences documentation in one intuitive, easy-to-use platform.

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 change management

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

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.

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

Learn how Docuvera will revolutionize your content capabilities