Medical Devices and the EU AI Act
Whitepaper: How to achieve a comprehensive compliance strategy

The EU AI Act places high demands on AI-supported medical devices. In the white paper "Medical Devices and the EU AI Act", we provide an insight into how you can adapt your compliance and market access strategies accordingly. Among other things, we focus on possible interactions with other national and international AI regulations. At the same time, we recommend that manufacturers use the new regulatory challenges to position themselves as pioneers for safety, efficacy and ethical AI development in medical technology.