The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
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 ...
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 ...
Brenner, who worked in the FDA’s Center for Devices and Radiological Health, will take the helm of the agency until a new ...
The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...
In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued two draft guidances on ...
With the FDA quietly rolling back DEI initiatives under Trump’s latest executive order, experts warn that underrepresentation ...
To address these shortages, the FDA has put measures into place, including expedited review processes and the use of enforcement discretion. The FDA also now requires manufacturers to give at least ...
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