AI in Drug Approval: The Controversy Surrounding FDA’s Elsa Tool
Robert F. Kennedy Jr., Secretary of Health and Human Services, advocates for using generative AI in drug approvals. However, a CNN report reveals alarming issues with the FDA’s AI tool, Elsa, which is said to produce “hallucinated” studies.
Key Insights:
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AI Tool Concerns:
- Elsa generates nonexistent studies, misleading summaries, and inaccurate information.
- Employees report it often requires human double-checking, negating claimed efficiency.
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Drug Approval Process:
- Kennedy claims AI could accelerate drug approvals but lacks clarity on implementation.
- Past reports from Kennedy’s commission cited numerous bogus studies.
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Industry Implications:
- Concerns arise over public health consequences if decisions are based on unreliable AI outputs.
AI’s potential is enormous, but as this situation illustrates, it’s crucial to prioritize accuracy over speed. What are your thoughts on AI’s role in healthcare?
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