What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.

The US Food and Drug Administration has approved the use of a novel painkiller as an effective treatment for short-term ...

On January 27, the U.S. Food and Drug Administration classified the recall as “Class I,” the most severe risk level. According to the FDA, “Class I” level recalls are used in situations ...

The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...

Guidance Shares Strategies to Address Transparency and Bias, while Providing Key Considerations and Recommendations on Product Design, Development and Documentation "The FDA has authorized more ...