Pharma Package, Variation Framework, ePI & more: Practical Labelling Impacts in 2026
This online conference covers key EU regulatory developments shaping labelling in 2026, practical best practices for compliant day-to-day labelling, progress on ePI and QRD updates, and the latest AI and automation applications in labelling workflows.
Topics:
- EU Pharma Package – Impact on Labelling
- New Variation Guideline – Practical Implications since January 2026
- QRD Template v10
- PPWR – Packaging & Packaging Waste Regulation
- ePI – Regulatory Developments & Practical Implications
- AI & Automation in Labelling
- Interplay of MDR, MPDG, HWG & Co
This two-day ExpertFORUM provides a structured, practice-oriented update on the key regulatory and operational developments shaping medicinal product labelling in 2026.
You will explore the impact of the EU Pharma Package on labelling requirements, discuss current implications of the Packaging and Packaging Waste Regulation (PPWR), and review how the new Variation Guideline affects day-to-day labelling operations.
European authority and industry experts will provide insights into the status of the QRD Template v10 and discuss challenges around artwork usability, urgent safety updates and error management. You will also gain insights into ePI implementation from a regulatory and practical perspective and the realistic role of AI and automation in labelling processes, including validation, GxP compliance and practical use cases.
Your benefit:
- First-hand updates on current topics from experienced labelling and regulatory professionals.
- Practical examples and expert insights on current EU developments.
- Valuable knowledge on innovative and digital approaches to labelling.
- Evaluate opportunities and risks of emerging technologies in labelling.