AI Regulation

…beyond Okta commit to the extension and whether any major enterprise SaaS vendors announce support independently. EU AI Act public consultation closes June 23 — four days remain; submissions citing the Fable 5 export control incident and Midjourney Medical's health claims are accumulating in the final week, with the last-day filing surge typically producing the most concrete accountability proposals. DiffusionGemma independent…

…without a clinical validation pathway is one that both FDA (under Software as a Medical Device) and EU AI Act reviewers are watching. Whether Midjourney Medical pursues formal regulatory clearance or positions itself as "informational only" will determine what it is legally permitted to claim — and whether this launch functions as a product or as a regulatory test case. Primary source: Midjourney Medical, June 18,…