FDA launches new AI-powered system to track drug and vaccine side effects nationwide
Fox News
FDA launches AI-powered Adverse Event Monitoring System to streamline health reporting. Commissioner Dr. Marty Makary says it will save $120 million.
Preston Mizell is a writer with Fox News Digital covering breaking news.
"The FDA’s fragmented adverse event systems have wasted taxpayer dollars and created large blind spots in our post-market surveillance," FDA Commissioner Dr. Marty Makary told Fox News Digital in a statement. "We’re addressing this critical issue by conducting a major modernization initiative on an accelerated timeline."
"Moving forward, the FDA will have a single, intuitive adverse event platform that will better equip us and any interested researcher to access key data and insights about the safety of products on the market," Makary added.
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