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Geoffrey Hinton Proposes FDA-Style Safety Approval Mechanism for AI Models

Turing Award winner Geoffrey Hinton proposed that AI companies should be legally required to prove model safety to regulators before public deployment, drawing a direct comparison to FDA drug approvals. He warned that rapid advancements driven by recursive self-improvement could significantly escalate AI safety risks within just one to two years. Hinton's call amplifies the ongoing global debate over mandatory government oversight and pre-deployment safety testing for frontier AI models. Requiring pharmaceutical-grade evaluation standards could fundamentally reshape development timelines and force companies to invest heavily in safety verification. Hinton noted that pharmaceutical drug approvals cost around a billion dollars in safety testing, suggesting AI safety evaluation demands comparable investment and oversight. He specifically cited recursive self-improvement—where AI tools are used to optimize and develop newer AI systems—as a primary accelerator of exponential risk.

## BACKGROUND

The U.S. Food and Drug Administration (FDA) requires pharmaceutical companies to complete rigorous multi-phase trials to prove safety and efficacy before market release. In artificial intelligence, recursive self-improvement describes AI systems enhancing their own code or architecture, which theoretical research suggests could trigger exponential capability gains and severe alignment challenges.

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## KEYWORDS

#AI Safety#AI Governance#AI Policy#Geoffrey Hinton

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Geoffrey Hinton Proposes FDA-Style Safety Approval Mechanism for AI Models | Daily News