The CISA and FDA have released security warnings about the Contec CMS8000, which is used for patient monitoring.

The Cybersecurity and Infrastructure Security Agency and Food and Drug Administration Jan. 30 released notices warning of ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

Pharma, biopharma, and medical device makers should watch out for these perennial problems, which include inadequate ...

Vulnerabilities in certain Contec and Epsimed patient monitors can allow people to gain access and potentially manipulate the ...

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

The FDA says the cybersecurity vulnerabilities identified may put patients at risk when the device is connected to the internet.

CISA and FDA say Contec patient monitors used in the US contain a backdoor that could allow remote attackers to tamper with the device.

Today, the U.S. Food and Drug Administration (FDA) issued a safety communication to raise awareness about cybersecurity ...

The Centers for Medicare and Medicaid Services ("CMS") published a final notice outlining the processes and procedures for the Transitional ...

The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with ...

With the FDA quietly rolling back DEI initiatives under Trump’s latest executive order, experts warn that underrepresentation ...