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A new article in the Journal of the American Medical Association said the FDA will implement AI into multiple processes.
FDA Commissioner Marty Makary and CBER Director Vinay Prasad published an article in JAMA on Tuesday outlining the FDA’s ...
AI is slowly permeating all corners of the federal government, including the Food and Drug Administration, where, according ...
This story is from the next print edition of MIT Technology Review, which explores power—who has it, and who wants it. It’s ...
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Medpage Today on MSNFDA Officials Lay Out Vision for AgencyThe new FDA commissioner and Center for Biologics Evaluation and Research (CBER) director laid out their vision for the ...
Makary and Prasad also repeat various themes repeatedly visited by Kennedy on his Make America Healthy Again (MAHA) soapbox, ...
The Food and Drug Administration has gone all in on AI since Martin Makary, M.D., took over the agency, most recently ...
The FDA plans to “rapidly make available” rare disease drugs and make use of surrogate endpoints to get promising medicines ...
The Food and Drug Administration (FDA) is looking to AI to solve the problem of lengthy approval processes, as the Trump ...
The U.S. Food and Drug Administration (FDA) says it plans to use artificial intelligence (AI) to help speed the approval of ...
The FDA has launched a pilot program using generative AI to help expedite the review of drug and device applications, part of a sweeping modernization effort by the agency. The initiative, led by FDA ...
Fears about the FDA imposing steep barriers to gene therapies for rare diseases appeared moot at an agency roundtable ...
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