Webinar: Content Governance in the Age of AI: Preparing Pharma for ePI and FHIR

Details

Docuvera and NNIT will host a webinar focusing on 'Content Governance in the Age of AI.' The core premise is that various regulatory mandates—such as ePI/FHIR, IDMP/SPOR, ICH M11, PQ-CMC, and EU ePL—are converging on a single operational requirement: structured, machine-readable content as a compliance imperative. Given the accelerating adoption of AI across enterprises, supporting governed content architecture is becoming increasingly urgent. The session aims to provide participants with: 1. A clear map of regulatory mandates and operational timelines forcing action. 2. Understanding why interoperability and AI are necessary but insufficient, detailing what the governed content layer must achieve. 3. Practical architectural guidance, including data contracts, schema validation, human acceptance gates, and FHIR integration in production. 4. Implementation sequencing designed to reduce validation risk and avoid common program failure modes. The target audience includes leaders (Director through VP) in pharmaceutical organizations across Regulatory Affairs, Labelling, CMC, Clinical, Safety, IT, and Digital Transformation.