![](https://medicaldevices.ipn.pt/wp-content/uploads/2024/07/Captura-de-ecra-2024-07-18-as-13.46.49.png)
The European Parliament has given the green light to the EU AI Act!
But what does this mean? The regulation awaits the final review and adoption before the legislative session ends, with Council endorsement still to come. Once published, it activates in just 20 days, but full implementation won’t happen overnight – we’ve got a timeline: prohibited practices are out in 6 months, followed by codes of practice in 9, general AI rules in 12, and high-risk system obligations in 36 months.
Why is this important? The approval of the EU AI Act represents a key step in aligning technological progress with the protection of fundamental rights. It highlights the EU’s dedication to setting standards in ethical AI practices, offering a model for responsible innovation and providing a reference framework for other regions.
Curious about our expertise in AI within the Medical Devices field? 💡 Dive deeper at our site: https://lnkd.in/dreiWTp7