PANEL DESCRIPTION
In 2020, the European Commission envisioned AI as a life-changing force by improving healthcare. Nowadays, AI applications have become integral to the provision of healthcare and medical research. Qualified as medical devices, numerous medical AI applications have been approved by the regulatory authorities both in the EU and the US across various domains such as radiology, cardiology, ophthalmology, gastroenterology, and neurology. The panel will discuss the state-of-the-art advancements and utilisation of AI in healthcare. It will explore the existing regulatory landscape of AI applications, along with the remaining ethical and legal challenges, as well as the role of the AI Act in addressing them. Speakers representing patients, healthcare professionals and institutions, regulators, and policy-makers will share their experiences and perspectives, thus facilitating a cross-sectoral dialogue and fruitful exchange of ideas.