Webinar on-Demand

Exploring the FDA's Sep 23Cybersecurity Guidelines

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Chris Gates

Director of Product Security

Guy Gilam
Guy Gilam

Head of Product Marketing

It’s here.

The new long-anticipated FDA cybersecurity guidelines titled Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions were released on September 27th.

With an invigorated approach and legislative backing, the FDA is strongly advocating that the ecosystem get in line with SBOMs, vulnerability management, and the way we share information. While you are eager to comply, do you know how?

In this webinar, we’ll explore the critical differences between old and new guidelines that manufacturers, vendors, and healthcare facilities must be aware of. Here are some of the main differences we’ll cover: 

  • Interoperability - How external machine-to-machine communications impact cybersecurity and what the FDA suggests to do about it

  • Vulnerability identification - What data sources and frameworks manufacturers should align with

  • Harmonizing product security and quality systems - How these two processes should come together

  • And more
In this webinar you'll learn about:
  • Group 6870

    The differences between the April 2022 draft and the final September 2023 guidance

  • Identify potential impacts on supply chain management icon

    What’s new for manufacturers and suppliers

  • Group 6949

    How to comply

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