| Session | ||
32a. Status of implementation of the MDR and consequences for medical device industry in Germany
Panel Discussion
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| Session Abstract | ||
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Panel discussion on medical device regulation, featuring distinguished experts from industry, academia, and regulatory bodies. They will share their insights and perspectives on the German view of medical device regulatory (MDR), compliance, and innovation. Parts of this event will be held in German. | ||
| No contributions were assigned to this session. |