Tridion One

Turn pharma regulatory complexity into your competitive advantage.

Eliminate the delays and risks of legacy authoring, ensuring that next-generation treatments reach the patients that need them most, with our AI-ready structured content authoring solution.

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Why Tridion One?

While electronic documents mimic the familiarity of print, they are increasingly unfit for purpose in a progressively digital world. It is time to modernize document and template management with a secure, end-to-end solution designed for the AI era. Leveraging structured content, our online platform replaces general-purpose word processing with integrated AI-driven authoring, review, translation, collaborative workflows, and project management.

Content building blocks (components) instead of monolithic documents

Content reuse and automatic data ingestion instead of copy/paste duplication

Generative AI for creating first-time-right drafts faster

Dynamic output for each use case (e.g., new layout or file type for the same content)

Learn how you can accelerate regulatory submissions with AI and content reuse

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Use cases

Clinical

Create and update even the most complex documents more efficiently across the clinical development cycle, with granular content reuse and other automations that minimize manual effort and error. From study protocols to manuals and clinical study reports, you’ll produce more consistent and accurate documents, significantly faster.

Regulatory

Simplify submission preparation with automated data ingestion, approved content reuse, precise version control, reliable audit trails and dynamic output from a single source – directly into your RIM system or to any other destination – all of which minimize risk and help you respond faster to regulatory change.

Manufacturing

Transform the creation of critical CMC documentation with sophisticated workflow controls that help stakeholders focus just on their piece of the puzzle in a timely manner. Also tailor to different local requirements, including translations, with the help of highly automated control of content variations.

Quality

Maintain global SOP libraries with local variants derived from shared sources of reusable content. Streamlined templates and data-driven content transform workflows by helping users quickly generate validation protocols, reports and ensure consistent terminology across thousands of documents, such as data integrity statements, deviation handling steps, cleaning procedures and more.

Demo videos

Solution info.

Tridion One – Templates

Tridion One automates the creation of regulatory documents by using templates. Watch the demo to see how teams can simplify submission preparation with automated data ingestion across the entire product lifecycle.

Solution info.

Tridion One – Working Documents

With the help of structured content authoring and content reuse through smart fields, experts edit, review and approve regulatory content faster. Discover how data-driven documents can help pharma innovate with confidence.

Solution info.

Tridion One – Preview and Outputs

Watch the demo to see how you can generate quick previews of working documents. With Tridion One’s single sourcing capabilities it is easy to generate regulatory documentation in any format DOCX, PDF, XML or FHIR.

Key benefits of Tridion One

Generate first drafts faster with AI.

Shrink authoring time by using pre-approved content and leveraging the large language model (LLM) of your choice to generate a first draft for narrative text chunks. Significantly slash authoring, review and approval times.

Collaborate more easily.

Improve quality and streamline processes by allowing authors, reviewers and SMEs to work collaboratively in real-time in an intuitive, purpose-built tool. Any number of users can work on the same document, no matter how complex or lengthy, and use comment threads to exchange feedback.

Improve content consistency and variation control.

Enable editors to reuse pre-approved content, so they never waste time again rewriting existing content for different variations of a document. With Tridion One, it’s easy for editors to see when content or data changes, so they can decide whether or not to propagate it automatically through all applicable documents.

Translate faster and cheaper.

Tridion One supports efficient translation by tracking the relationships between source and target language. With a single source of truth, you can maintain full traceability of all language versions, while also making documentation easy to update and audit-ready by design.

Save time and effort with automated output.

From a single working document, you can generate different types of output (such as Word, PDF, XML, JSON, FHIR) and apply various output templates to produce specific document layouts and designs. You can also push files to connected systems, such as your RIM system, or give applications, such as AI-powered services, access to your structured content.

Comply with a smile.

Reduce risk and simplify compliance with vastly improved content consistency, dependable translations, precise version control and reliable audit trails that track all changes in each content component, working document and output file.