DAILY Bites
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FDA launches Elsa AI tool to improve efficiency and support scientific reviews.
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Runs in secure GovCloud, protecting internal and industry data.
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First step in broader AI plans, with future expansions already underway.
DAILY Discussion
The machines are moving into federal food policy. Today, the U.S. Food and Drug Administration launched Elsa, a generative Artificial Intelligence tool designed to help employees work more efficiently. This agency claims that the tool will modernize agency functions and leverages AI capabilities to better serve the American people.
“Following a very successful pilot program with FDA’s scientific reviewers, I set an aggressive timeline to scale AI agency-wide by June 30,” said FDA Commissioner Marty Makary, M.D., M.P.H. “Today’s rollout of Elsa is ahead of schedule and under budget, thanks to the collaboration of our in-house experts across the centers.”
Built within what the agency says is a high-security GovCloud environment, Elsa’s platform allows FDA employees to access internal documents while ensuring all information remains within the agency. The models do not train on data submitted by regulated industry, safeguarding the sensitive research and data handled by FDA staff.
“Today marks the dawn of the AI era at the FDA with the release of Elsa, AI is no longer a distant promise but a dynamic force enhancing and optimizing the performance and potential of every employee,” said FDA Chief AI Officer Jeremy Walsh. “As we learn how employees are using the tool, our development team will be able to add capabilities and grow with the needs of employees and the agency.”
The FDA plays a significant role in agriculture and food policy, helping to establish rules, standards, and guidance, particularly in the realm of food safety. The agency often works closely with the U.S. Department of Agriculture.
The agency is already using Elsa to accelerate clinical protocol reviews, shorten the time needed for scientific evaluations, and identify high-priority inspection targets.
Elsa is a large language model-powered AI tool designed to assist with reading, writing, and summarizing. It can summarize adverse events to support safety profile assessments, perform faster label comparisons, and generate code to help develop databases for nonclinical applications. These are just a few examples of how Elsa will be used across the enterprise to improve operational efficiency.
The introduction of Elsa is the initial step in the FDA’s overall AI journey. As the tool matures, the agency says they have plans to integrate more AI in different processes, such as data processing and generative-AI functions to further support the FDA’s mission.
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