The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...
The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...
Robert F. Kennedy Jr., President Donald Trump's pick to lead the top U.S. health agency, told U.S. senators during his ...
Following the Trump administration's DEI ban, the FDA's move to scrub webpages has ensnared many pages focused on ensuring ...
Brenner, who worked in the FDA’s Center for Devices and Radiological Health, will take the helm of the agency until a new ...
Hologic Inc. has received a warning letter from the Food and Drug Administration regarding its BioZorb product line, even though the company recalled the devices last year.
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
By establishing coding and separate payment for certain digital mental health devices, this group from CMS and the FDA hopes ...
The Food & Drug Administration (FDA), has quietly taken down their guidance detailing diversity action plans for clinical ...
If you have a microcurrent device on your wishlist, here are some benefits and drawbacks to consider before you buy one.
The Food and Drug Administration (FDA) has recently released two draft guidance documents (Artificial Intelligence-Enabled Device Software ...
In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued ...