Introducing Tridion One: From documents to data-centric regulatory submissions for pharma
On-Demand Webinar
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. This also results in content that’s less available to your organization, and not optimized for AI-based approaches, or for use and submission in modern formats including JSON or HL7 FHIR.
Tridion One is an end-to-end structured content authoring and content management platform that breaks down documents and publications into components that are Findable, Accessible, Interoperable and Retrievable (FAIR). Narrative content that has been optimally componentized and curated improves the performance and accuracy of Generative AI-based approaches.
Join Todd Georgieff, Tridion One Lead for Pharma, and Patrice Canonne, Principal Solutions Consultant, to see how Tridion One has been developed to fully support pharma content across key business areas:
- Chemistry, Manufacturing and Controls (CMC) or Module 3 of the CTD
- Labelling information, including ePI and eLabelling
- Clinical use cases including Informed Consent, Study Protocols and other study documentation
Discover the resources from this webinar, and find out more about Tridion One, below.
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