What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
Following the Trump administration's DEI ban, the FDA's move to scrub webpages has ensnared many pages focused on ensuring ...
In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued ...
Vulnerabilities in certain Contec and Epsimed patient monitors can allow people to gain access and potentially manipulate the ...
The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with ...
Our FDA/Food, Drug & Device and Health Care teams discuss new guidance from the Food and Drug Administration (FDA) on federal notification requirements for medical device manufacturing shortages ...
With the FDA quietly rolling back DEI initiatives under Trump’s latest executive order, experts warn that underrepresentation ...
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
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 ...
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The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...
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 to improve access to care.
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