Understanding Cyber Devices in Healthcare - Part 2 of 2

This on-demand webinar talks about what it means for a medical device to be a cyber device from the perspective of software risks.

THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

Watch the video: Healthcare Cybersecurity

Why is the term “cyber device” suddenly so important? What does the “cyber” prefix really mean? What kinds of risks are unique to a cyber device and differentiate it from other types of medical devices?

Recent legislative changes, including amendments to the U.S. Food Drug & Cosmetic Act, under which the U.S. Food and Drug Administration (FDA) exercises its authorities, have spurred a growing interest in this topic. The recent FDA guidance on its Refuse to Accept policy provides insights into what it means for a medical device to be a cyber device.

Webinar date: Nov. 16, 2023
Speaker: Anura Fernando, principal security advisor

In this webinar, UL Solutions experts will discuss what it means for a medical device to be a cyber device, the importance of cyber devices and approaches to protecting them.

Learning objectives

•   Provide background information about the term “cyber”
•   Discuss what governments are doing to manage risks with cyber devices
•   Take a technical deep-dive into cyber device attributes
•   Explore practical approaches to managing cyber devices
•   Discuss tools and resources to help secure medical devices

Watch the video: Advancing Cybersecure Medical Devices - Part 1 of 2

Why is the term “cybersecure” suddenly so important? What does the “cyber” prefix really mean? How “secure” is “secure enough”? How do I plan for cybersecurity in my organization? What tools are available to help me produce “cybersecure” medical devices?

In this on-demand webinar, we talk about what it means for a medical device to be “cybersecure.” This is a topic that is currently of significant interest because of the recent legislative changes including amendments to the US Food Drug & Cosmetic Act, under which the US FDA exercises its authorities. The recent FDA guidance on their “Refuse to Accept” policy provides some insights into what it means for a medical device to be “cybersecure.” We discuss the importance of the total product lifecycle in managing cybersecurity of medical devices, including post-market issues like their end-of-life, end-of-support, decommissioning, and disposal.

Webinar date: June 27, 2023
Speaker: Anura Fernando, principal security advisor