Introducing Tridion One: From documents to data-centric regulatory submissions for pharma

Introducing Tridion One: From documents to data-centric regulatory submissions for pharma
Fonto One is now Tridion One. We invite you to join us for the next chapter of our AI-enabled Structured Content Authoring platform, purpose-built for Pharma.. Until now, Regulatory Documentation has been created, reviewed, published and managed in the form of thousands of static documents. Processes to author, update and validate information stored this way are slow, costly, and lack scalability.