FDA将在全机构范围内部署人工智能。
FDA To Deploy Artificial Intelligence Across Agency

原始链接: https://www.zerohedge.com/technology/fda-deploy-artificial-intelligence-across-agency

美国食品药品监督管理局(FDA)正在迅速将其所有中心整合人工智能(AI),目标是在六月底之前全面完成整合。此举是在一个成功的试点项目之后进行的,由FDA局长Marty Makary博士推动,他强调需要使该机构现代化并缩短新疗法的审查时间。 所有中心都将使用一个安全、通用的生成式AI系统,该系统连接到FDA的内部数据平台。目标是简化流程,一些以前需要几天才能完成的任务现在可以在几分钟内完成。此次推广由FDA新的首席AI官Jeremy Walsh和Sridhar Mantha协调。 此举与更广泛的美国政策相符,包括特朗普和拜登政府都鼓励在政府机构中采用AI。FDA承认过去对AI偏差的担忧,但认为其实施可以显著加快药物申请审查,最终改善患者获得药物的机会。


原文

Authored by Zachary Stieber via The Epoch Times (emphasis ours),

The Food and Drug Administration (FDA) is planning to roll out artificial intelligence across the agency following a successful pilot program.

The U.S. Food and Drug Administration (FDA) in White Oak, Md., on June 5, 2023. Madalina Vasiliu/The Epoch Times

FDA Commissioner Dr. Marty Makary has directed all FDA centers to immediately start using artificial intelligence (AI) and fully integrate it by the end of June, the FDA said in a May 8 statement.

By June 30, all centers will use what the agency described as a “common, secure generative AI system integrated with FDA’s internal data platforms.”

“I was blown away by the success of our first AI-assisted scientific review pilot,“ Makary said in a statement. ”We need to value our scientists’ time and reduce the amount of non-productive busywork that has historically consumed much of the review process. The agency-wide deployment of these capabilities holds tremendous promise in accelerating the review time for new therapies.”

AI refers to computer systems that can carry out complex tasks typically performed by humans.

“AI can be generally described as a branch of computer science, statistics, and engineering that uses algorithms or models to perform tasks and exhibit behaviors such as learning, making decisions, and making predictions,” FDA officials said in 2023.

Makary said on Thursday that past years have featured discussions on utilizing AI and that it’s time to start using it to save time, with some tasks that once took days now taking mere minutes.

“We at the FDA now have to ask big questions that we’ve never asked before. Why does it take over 10 years for a new drug to come to market? Why are we not modernized with AI and other things? We’ve just completed our first AI-assisted scientific review for a product and that’s just the beginning,” he said earlier in the week on social media platform X.

The rollout across the FDA is being coordinated by Jeremy Walsh, Booz Allen Hamilton’s former chief technologist, who was recently appointed as the agency’s chief AI officer, and Sridhar Mantha, who previously led the Office of Business Informatics at the FDA’s Center for Drug Evaluation and Research.

President Donald Trump has encouraged agencies to adopt wider use of AI, including through an executive order that said it is U.S. policy to “sustain and enhance America’s global AI dominance in order to promote human flourishing, economic competitiveness, and national security.”

An April memorandum from the White House said that agencies “must adopt a forward-leaning and pro-innovation approach that takes advantage of this technology to help shape the future of government operations.”

The FDA had previously expressed concern that AI contains bias that may “worsen inequalities in health care delivery,” while also saying AI could speed up review of drug applications to bring quicker timelines for making drugs available to patients.

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