Upcoming Webinar | June 10, 2026
Webinar: Content Governance in the Age of AI: Preparing Pharmaceutical Organisations for ePI and FHIR I by Docuvera & NNIT
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ePI/FHIR, IDMP/SPOR, ICH M11, PQ-CMC, and EU ePL are converging on the same operational requirement: structured, machine-readable content as a compliance imperative.
The accelerating adoption of AI across the enterprise makes the architecture to support governed content more urgent, not less.
Join regulatory and content governance specialists from Docuvera and NNIT for a practical session on what it takes to make enterprise intelligence regulatory-grade: governed, traceable, structured, and submission-ready at scale.
You will leave with:
A clear map of the regulatory mandates and operational timelines forcing action
Why interoperability and AI are necessary but not sufficient, and what the governed content layer must do that neither can
Practical architecture guidance: data contracts, schema validation, human acceptance gates, and FHIR integration in production
Implementation sequencing that reduces validation risk and avoids the failure modes that stall most programmes
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Speakers
Murali Menon, Chief Revenue Officer, Docuvera
Alexandra Antczak, Regulatory Affairs and Clinical Expert, NNIT
Emilie Troldborg Hansen, Regulatory Affairs Consultant, NNIT
Who is this session for?
Regulatory Affairs, Labelling, CMC, Clinical, Safety, IT, and Digital Transformation leaders (Director through VP) in pharmaceutical organisations.
Contact
If you have any questions regarding the webinar, please do not hesitate to contact Anne Amalie Barbosa-Merrild at aabm@nnit.com.
