Structured Component Authoring to Accelerate Compliant Content Creation

An intelligent SaaS solution that combines automation and necessary governance to author, review, approve, translate, and publish regulated documents

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Docuvera is a globally recognized content management solution provider in the life sciences sector, specializing in structured component authoring and management.

With Docuvera, organizations streamline the creation, review, translation, and approval of regulated content – for greater accuracy and reduced time spent. Thanks to a deep understanding of industry challenges, Docuvera seamlessly integrates compliance-driven workflows with the latest technology, driven by Artificial Intelligence (AI), to optimize regulatory, quality, clinical, and safety documentation processes.

Trusted by leading life sciences companies, Docuvera ensures efficient collaboration, version control, and audit readiness while meeting stringent global regulatory requirements.

Content reuse

Productivity gains

Years of innovation in life sciences

The Most Efficient Way to Author Life Sciences Documentation

Docuvera addresses a key challenge in the life sciences industry – efficiently creating and updating documentation throughout the drug development lifecycle.

By breaking down documents into component structures, the comprehensive platform empowers its users to save time and increase efficiency during authoring. All related processes benefit from this innovative approach as well: reviewing, approving, translating, and publishing are significantly accelerated. Streamlining these processes with Docuvera’s combined AI + structured content technology quickly results in a rise in productivity, guaranteed compliance, and faster time-to-market.

Cutting-edge Technology to Maintain Operational Excellence across Formats and Channels

Built on a structured content framework, Docuvera enables seamless content reuse, eliminating the inefficiencies of manual copy-and-paste processes while maintaining consistency across all documents.

The integrated web-based review and approval process enhances collaboration across teams, enabling faster decision-making in a single, centralized workspace. Once finalized, documents can be published in multiple formats—including Word, PDF, and HTML—directly from the platform, ensuring efficient content delivery across all regulatory and commercial channels.

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Content Creation Powered by Artificial Intelligence (AI)

AI-powered automation enables authors to efficiently assemble compliant documents using pre-approved content blocks.

Real-time updates notify teams of changes, ensuring consistency and reducing the risk of errors from manual copying. With an intuitive interface and seamless structure, users can easily transition from traditional solutions or desktop-based workflows.

Seamless Integrations for Enhanced Flexibility and Compliance

Docuvera seamlessly integrates with third-party products, enhancing content management and regulatory compliance while adapting to customers' existing infrastructure.

Supporting tools like Veeva Vault, Microsoft SharePoint, and EXTEDOpulse, these integrations streamline workflows, ensure consistency, and reduce manual effort. By automating data exchange, Docuvera enables life sciences organizations to improve efficiency, maintain compliance, and accelerate their time-to-market.

What they say about us

Docuvera is a growing, innovative technology. I really appreciate the team’s responsiveness to our needs. Migration of existing content in Docuvera is a big piece for the adoption, and it helps authors adopt the solution when they see their content in the new technology.

Cecil Lee,
Position Senior Director, Content Intelligence Team, Lilly

Docuvera came with a different approach that was far more flexible. Using the structure, the ability to reuse content and consistency — it gets rid of inflexible things.

Holger Christstein,
Senior Business Consultant and Senior IT Project Manager, Boehringer Ingelheim