"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 ...
Following the Trump administration's DEI ban, the FDA's move to scrub webpages has ensnared many pages focused on ensuring ...
Robert F. Kennedy Jr., President Donald Trump's pick to lead the top U.S. health agency, told U.S. senators during his ...
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 ...
As AI in the medical device space rises, it likely means 2025 will be another challenging year for cyber threats in ...
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
The Food & Drug Administration (FDA), has quietly taken down their guidance detailing diversity action plans for clinical ...
New documents clarify how the FDA plans to regulate AI-enabled devices, experts say, but several important questions remain ...
The FDA’s Webinar for Manufacturers and Other Interested Parties - The U.S. Food and Drug Administration (FDA) will host a webinar ...
The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...
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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