Impacts of AI on the Development of Medical Devices

Artificial intelligence (AI) is revolutionizing medical engineering by improving diagnostics and streamlining healthcare. Advances in machine learning, such as neural networks, have opened the door to new possibilities. However, regulatory frameworks significantly impact the use of AI in medical devices and their deployment in healthcare.

Join this webinar as our experts discuss the impacts of AI on the development of medical devices. We will cover timely topics, including:

• The European Union (EU) AI Act requirements for safety and ethical standards in AI applications.
• U.S. Food and Drug Administration (FDA) guidelines for the safety and effectiveness of AI technologies.
• Addressing data privacy challenges and bias in AI.
• Evolving AI regulations aiming to prevent errors and ensure reliable AI performance in medical settings.
• Emerging technologies such as generative AI and natural language processing (NLP) poised to further transform healthcare and improve its affordability and accessibility.
• The importance of collaboration and training for healthcare professionals and engineers to foster innovation.

We’ll conclude with a Q&A session to address your questions.

Speakers

Christian Lederer is an engineering manager at UL Solutions - Software Intensive Systems. With his team, he supports clients in the development of medical devices. For several years, his main focus of interest has been functional safety and regulations in medical technology.

Florian Gabsteiger is a principal software engineer at UL Solutions - Software Intensive Systems. His main focus areas are AI, functional safety and software architecture. He supports customers in safety-critical fields, including healthcare and automotive.