Turn 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 for pharma.
It’s time to move beyond managing documents and embrace the future: AI-ready structured content.
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Step into the era of AI-enabled structured content authoring
Electronic documents have been around for decades. As humans, we like them because they mimic printed materials. But they are static, highly inefficient and provide poor input for AI-driven processes. Instead, the pharma industry needs a new approach that allows organizations to break down massive documents into smaller components that are Findable, Accessible, Interoperable and Retrievable (FAIR).
It's time to adopt an end-to-end, secure, structured content authoring and management platform
You can work faster with
Content building blocks (components) instead of monolithic documents
Generative AI for creating first-time-right drafts faster
Content reuse and automatic data ingestion instead of copy/paste duplication
Dynamic output for each use case (e.g., new layout or file type for same content)
Key benefits of using 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.
Collaborate more easily
Improve quality and streamline processes by allowing authors, reviewers and SMEs to work collaboratively in real-time in an intuitive Word-like tool.
Improve content consistency
Enable editors to reuse pre-approved content components, so they never waste time again rewriting existing content for different variations of a document.
Translate faster and cheaper
Combined with the RWS translation management system (TMS) supports efficient translation by tracking the relationships between source and target language components.
Save time with automated output
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.
Comply with a smile
Reduce risk and simplify compliance audit trails that track all changes in each content component, working document and output file.
Discover Tridion One today
Get in touch to discover how you can 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 for pharma.
Talk to an expert
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