The Food and Drug Administration has issued draft guidance urging medical device manufacturers to develop cybersecurity controls in the design phase of their product development. The guidance ...

Mobile devices have become indispensable in hospital workflows, making well-designed security strategies essential.

The latest update to the Federal Drug Administration (FDA) for medical device cybersecurity mandates the development of a software bill of materials (SBOM). This provision can be a significant ...

A new report casts light on the security challenges and spending patterns of cybersecurity leaders in healthcare. The survey – based on a poll of more than 600 healthcare IT decision-makers who play a ...

The growing sophistication of medical devices make it likely that 2025 will be another challenging year for cybersecurity and ...

How would you grade your organization’s cybersecurity? A new report does just that, and the results are concerning for medical device companies. Overall, healthcare gets a passing B+, but medical ...

The software supply chain is critical to ensuring a secure medical device that can prevent injury, according to Gregg Van Citters, MS, PhD, a principal software quality engineering consultant at ...

Newly updated Food and Drug Administration guidelines will help experts to more accurately score and communicate the criticality of security vulnerabilities identified in medical devices, says Elad ...

In 2018, FDA took steps to build Software Bill of Materials into premarket medical device approvals, making them more secure against potential attacks. SBOMs have since become a cornerstone for ...

Imprivata’s survey found that 85% favour passwordless authentication, yet adoption lags due to technical and integration-related challenges.

After decades of accepting cybersecurity as someone else’s problem, healthcare buyers have reached a turning point. Where cost and functionality once dominated purchasing decisions, cybersecurity ...