Join us for a 90-minute webinar, hosted by AdvaMed, focusing on the new EU Medical Device Regulations (MDR/IVDR), which represent the single largest regulatory change in the EU in decades. This program will highlight what the regulatory changes are, how these changes will affect your business, and what you can do to better prepare. In particular, the classification rules for software have changed, and new requirements are likely to apply to apps and mHealth technologies.
Agenda topics include:
- What are the changes in the regulations?
- How will these changes affect research and development, and what impact will there be on, among other things, mobile and telemedicine?
- How will the new framework affect market access?
Click here to register.