Exploring the FDA's Sep 23Cybersecurity GuidelinesWatch Now
Director of Product Security
Head of Product Marketing
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
The differences between the April 2022 draft and the final September 2023 guidance
What’s new for manufacturers and suppliers
How to comply