News
Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and ...
In 2023 Dr. Vinay Prasad said that scientists who recognized the limitations of randomized-controlled trials (RCTS) were ...
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 ...
The FDA’s accelerated approval pathway plays a vital role, and scrapping it or reversing course on already-approved therapies ...
In case you haven't had enough artificial intelligence, the US Food and Drug Administration is now outsourcing its oversight duties to a large language model (LLM.) In an article published in the ...
Explore more
AI is slowly permeating all corners of the federal government, including the Food and Drug Administration, where, according ...
Last Thursday during a roundtable on stem cell therapies, new FDA Commissioner Marty Makary referred to EBM levels of evidence as an artificial and dogmatic construct. Apparently Dr. David Katz's "mor ...
When two of medicine’s most outspoken reformers publish a roadmap for the FDA, you expect at least coherence. Instead, we get ...
1d
Clinical Trials Arena on MSNPolicy changes and digital strategies guide oncology researchAt the CTO West Coast conference, experts discussed the future of oncology clinical trials and key themes surrounding them.
With a Trump-driven reduction of nearly 2,000 employees, agency officials view artificial intelligence as a way to speed ...
The Food and Drug Administration has gone all in on AI since Martin Makary, M.D., took over the agency, most recently ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results