OCT Medical Devices 2025: European AI Act compliance ‘not a cause for panic’
For those with Class IIa or above AI-related devices, compliance with the EU’s AI Act is likely to be akin to the EU MDR.
29 January 2025
29 January 2025
For those with Class IIa or above AI-related devices, compliance with the EU’s AI Act is likely to be akin to the EU MDR.
When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of data input.
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10xBeta CEO Marcel Botha talks about the FDA’s plans for medical shortage notifications and how Trump’s policies may impact US supply chains.
Up to 120 subjects will be enrolled in the study across 20 sites in the US.
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Nobi’s lamp combines AI and optical technology to expedite fall alerts and prevent them happening in the first place.
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