Creating an AI committee within a company’s governance framework on the usage of artificial intelligence is no longer a luxury, it is a necessity.
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The European Commission's GPAI guidelines under the AI Act are here—and they’re about to change how general-purpose AI models are developed, distributed, and regulated in the EU. If you work with large language models, generative AI systems, or provide AI tools to customers in the European Union, these guidelines define the rules you’ll need to follow from 2 August 2025.
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Artificial intelligence is rapidly transforming the life sciences sector — and its impact on the medical devices industry is particularly significant, especially after the coming into force of the EU AI Act. From diagnostics to patient monitoring and personalized treatments, AI-powered medical technologies are reshaping the future of healthcare in Italy, Europe, and globally. But as innovation accelerates, so does the need for a robust legal framework — especially under the recently adopted AI Act.
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The European Commission has launched a targeted consultation to support the development of Guidelines for implementing the AI Act, inviting all relevant GPAI stakeholders to submit their input via a survey until May 22, 2025.
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