Talk
Exploring the future of medical device and drug combination products: insights from EMA and key considerations for MR and MDR compliance
Tue, Jan 28, 2025 · 11:30 AM–12:00 PM CET Holiday Inn Munich City Centre
About this session
- Understanding the increasing trend of combining medical devices and drugs
- Gaining insights from the European Medicines Agency (EMA) on the future of medical device and drug combinations
- Explaining the distinction between Medical Devices Regulation (MDR) and Medical Devices Directive (MR) for combination products
- Identifying compliance requirements and implications based on the device's primary mode of action
- Presenting various regulatory pathways available for combination products
- Understanding how partnerships can drive innovation and development in this domain
