SHS Webinar on "AI in Healthcare: Navigating the EU AI Act and FDA Guidelines"

Artificial intelligence is revolutionizing healthcare, but how do you ensure innovation while maintaining patient safety?

In this webinar, medical device expert Dr. Rolf Kaufmann will provide an in-depth overview of the evolving regulatory landscape, focusing on the EU AI law and FDA guidance.

Emphasis will be placed on highlighting the key differences between traditional machine learning and generative AI, as well as between medical devices and general healthcare applications. You will learn how regulatory frameworks are adapting to protect patient safety while enabling medical innovation in the age of intelligent algorithms.

Join us to explore how regulatory frameworks are adapting to modern AI technologies and what this means for startups, innovators, and healthcare professionals.

Speaker

Dr. Rolf Kaufmann, Medical Device Expert at Effectum Medical

Rolf is a senior medical device expert with a focus on software and AI products. Prior to his current role, he cultivated his medical device expertise as a physicist, acquiring proficiency in X-ray technology, radio-oncology, image processing, and electronics.

About Effectum Medical

Effectum Medical facilitates an efficient, accelerated market access for MedTech innovators by offering a maintained Plug-and-play Quality Management System and when needed, acting as legal manufacturer. Their new Plug-and-play QMS is based on a modular concept where startups can pick and choose the services they require.

Program

13:00 Webinar starts
13:45 Q&A
14:00 End of the session

You are kindly requested to register only if you are planning on participating.
If you register and unfortunately can no longer attend, we kindly ask you to drop us an email to diana@swisshealthcarestartups.com.

⚠️ Registration deadline: March 10, 2025 ⚠️