The medical.device.forum 2026 organized by TÜV SÜD Academy is one of the most important industry gatherings for regulatory affairs, quality management, and risk and product management in the medical technology sector. Experts from industry, regulatory agencies, and Notified Bodies will discuss current developments related to the MDR, relevant standards, artificial intelligence, cybersecurity, and other regulatory requirements. The conference offers valuable insights into new requirements and practical solutions for day-to-day work.

BAYOOSOFT is also represented at the event. With BAYOOSOFT Themis, we help medical technology companies implement regulatory requirements efficiently and in a traceable manner. The software provides a central platform for managing regulatory information and helps teams document the entire product lifecycle in a transparent and audit-proof manner.

Take this opportunity to speak with us in person and use the form below to request a meeting. We’ll get back to you with a suggested time.