Die folgenden Informationen sind nur auf Englisch verfügbar:

During this webinar we will cover the following topics for the European and specifically the German market:

• An introduction to the new AI regulatory framework and its impact on the medical device industry, specifically risk classification, conformity assessment and certification.
• The importance of the AI Act for the development and use of artificial intelligence in medicine
• Data protection regulations for medical technology with AI and best practices for successful implementation.

Our experts will use practical examples to explain how the regulatory requirements of the AI Act interact with medical device regulations and what medtech companies need to consider. In addition, we will discuss the importance of data protection in this context and show how both manufacturers and users can use medical technology with AI in compliance with data protection regulations.

As a participant of the webinar, you will not only receive valuable insights and answers to your questions, but also the recording of the webinar and our exclusive white paper “The Interaction of Regulatory Affairs, AI and Data Protection in Medical Technology - 20 questions and answers”.

Register for free today and benefit from our in-depth knowledge and expertise in the field of digital health.