AI: a challenge for research, healthcare and industries

About this session

The presentation analyzes the role of AI in medicine, highlighting that the value of the technology depends more on regulation, quality, and governance than on innovation itself. AI, when integrated into medical devices, requires compliance with the MDR and AI Act, with a strong focus on clinical evaluation, safety, and reliability. Critical issues emerge related to high costs, data management, and the unequal distribution of benefits, with a prevailing advantage for technology players. In summary, the effective adoption of AI requires a regulated, sustainable ecosystem oriented toward clinical value.

Speakers

FG

Fernanda Gellona

Coordinatore esecutivo, Med Device Lab