All things considered, it’s at least as likely to make health outcomes worse as it is to make most people healthier.
Following the Trump administration's DEI ban, the FDA's move to scrub webpages has ensnared many pages focused on ensuring ...
The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...
In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued ...
The Food & Drug Administration (FDA), has quietly taken down their guidance detailing diversity action plans for clinical ...
"FDA grants 510(k) clearance to GE HealthCare’s updated ultrasound systems" was originally created and published by Medical Device Network, a GlobalData owned brand. The informa ...
Robert F. Kennedy Jr., President Donald Trump's pick to lead the top U.S. health agency, told U.S. senators during his ...
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
New documents clarify how the FDA plans to regulate AI-enabled devices, experts say, but several important questions remain ...
The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...
The US Food and Drug Administration (FDA) recently issued its draft guidance, Artificial Intelligence-Enabled Device Software Functions: ...
How the FDA and CMS worked together on a new approach to paying for digital mental health treatments
By establishing coding and separate payment for certain digital mental health devices, this group from CMS and the FDA hopes ...
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