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Direct involvement in PreCheck can shorten manufacturing timelines for LLY's GLP-1 ingredients, reducing risk of supply disruption and potentially enabling faster launches or scale-up; positive sentiment may follow, though actual timing remains uncertain.
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The FDA selected seven companies including Lilly and Regeneron for its PreCheck pilot to accelerate reviews of new manufacturing facilities, potentially saving up to 14 months. For Lilly, the Lebanon, Indiana GLP-1 ingredient facility could see timeline shifts if PreCheck improves inspection throughput, boosting domestic supply resilience.
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