Electronic Product Information (ePI) is reshaping the way pharmaceutical companies manage, distribute, and update product data—bringing new levels of agility, transparency, and accuracy to the industry. As regulatory bodies across Europe and beyond push for digital-first labeling strategies, ePI offers a dynamic solution for ensuring up-to-date, multilingual, and patient-accessible product information. In this session, you will learn how to:
- Enhance patient-centricity by enabling digital access to leaflets and safety information across devices and languages.
- Address regulatory readiness for ePI adoption, including EMA and national authority expectations.
- Explore the operational impact of ePI on packaging workflows, quality assurance, and version control.
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