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Description
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.
A new infrastructure that brings together innovation, services, and training with the aim of supporting research, creation, development, and certification for all health technologies.
