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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.

An image depicting a medical technology concept

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

 

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