- 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 LabellingThis 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.
LernzieleThis 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.ZielgruppenThis online conference is aimed at professionals working in regulatory affairs, medical affairs, pharmacovigilance, labelling/artwork and related functions who manage or contribute to medicinal product labelling processes.- It provides useful updates on the relevant trends in labelling. A working knowledge of product information and labelling is required.
- EU Pharma Package - Impact on Labelling - New Variation Guideline - Practical Implications since January 2026 - QRD Template v10 - PPWR - Packaging & Packaging Waste Regulation - ePI - Regulatory D... Mehr Informationen