European Medicines Agency at BIO-Europe 2026
Nov 9–11, 2026 Cologne, Germany ~5.8k attendees Website
European Medicines Agency takes part in 5 sessions at BIO-Europe 2026 in Cologne. Its sessions centre on how regulators and drug developers can work together to move new medicines forward. Topics include regulatory sandboxes for novel therapeutics and technologies, rules for AI, and the route to regulatory acceptance for new approach methodologies that model human biology.
| Organization | BIO-Europe 2026 Attendance |
|---|---|
European Medicines Agency Amsterdam, Netherlands | |
EU agency that evaluates and supervises medicines for human and veterinary use. | Panel Mon Nov 9 11:00–11:45 Unlocking Pharma’s Productivity Potential Why developing medicines keeps getting costlier and slower, and whether AI and research sourced from other companies can make drug companies more productive. Business of Biotech Panel Tue Nov 10 13:00–13:45 Aligning with Regulators to Propel Innovation What help and incentives the European Medicines Agency offers developers of new treatments, and how to use them on the road to approval. Panel Tue Nov 10 14:00–14:45 Harnessing Regulatory Sandboxes to Drive Innovation in Novel Therapeutics & Technologies How regulatory sandboxes, where regulators let new products be tested under adjusted rules, could support new therapies and health technologies in Europe. Panel Wed Nov 11 10:00–10:45 AI Regulations: Driving Innovation While Navigating Compliance What rules cover AI in drug development, where European and US regulators agree, and how rules could help rather than hinder innovation. Panel Wed Nov 11 09:00–09:45 From NAMs (New Approach Methodologies) Innovation to Regulatory acceptance: Accelerating human-relevant modelling How lab models built on human biology, from organs-on-chips to AI computer models, can speed drug development and win regulators' acceptance. |
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