Electronic Product Information (ePI) Resources

Everything you need to understand electronic Product Information (ePI) in the EU — from the FHIR-based common standard to the EMA's phased rollout for centrally authorised medicines

Helping regulatory, industry, and healthcare stakeholders stay ahead of the EU ePI transition.

Electronic Product Information (ePI) is transforming how medicines information — the Summary of Product Characteristics (SmPC), Package Leaflet (PL), and labelling — reaches healthcare professionals and patients across the European Union. Built on the EU ePI Common Standard and the global HL7 FHIR framework, ePI keeps authorised medicinal information accurate, searchable, and instantly accessible on the digital platforms people already use.

With the EU's new pharmaceutical legislation (political agreement, December 2025) and the EMA's phased rollout roadmap (published March 2026) now defining concrete timelines for Centrally Authorised Products, life sciences organisations need clear, reliable guidance.

This resource hub brings together cormeo's ePI Masterclasses, infographics, blog posts, and regulatory timelines to help you navigate ePI — from the underlying data standard to what's changing, and when.