Navigating FDA submissions is a make-or-break process for your medical device company’s revenue. But today, cybersecurity is a key component in protecting your product on the market. It's no longer just a checkbox — it’s a continual, critical effort. Here’s the catch: one size doesn’t fit all when it comes to cybersecurity. So, how can the FDA require eight specific security control categories for every medical device? 

The answer lies in finding the right balance. You need to combine a common baseline with security features tailored to the unique risks your device faces. Join us for the latest webinar in our exclusive Cybersecurity in Medical Devices series, where we’ll dive deep into how to balance these mandatory security control categories for successful FDA 510(k) submissions.

Here’s what you’ll learn:

• The 8 key security categories that the FDA mandates for medical devices
• How to tailor security to your device’s specific risks while maintaining that critical baseline
• Real-world examples of medical devices, their attack surfaces, and how the FDA categories map to mitigate risk

Don’t miss out on this valuable session that could make all the difference in getting your product to market securely and successfully. Sign up now and get the practical advice you need to ace your 510(k) submission!