Bringing a medical device to market? You’ll need more than a great product - you’ll need a cybersecurity strategy that meets today’s FDA expectations
Join Medcrypt CEO Mike Kijewski and VP of Regulatory Services Naomi Schwartz as they walk you through the basics of medical device cybersecurity. We’ll cover what it actually takes to secure your device, how cybersecurity fits into the FDA submission process, and what steps you can take now to avoid delays later. Whether you’re new to cybersecurity or just need a gut check before your next submission, we’ll break it down in a way that’s easy to understand.
What You’ll Learn:
- Why cybersecurity is now a must-have for device approval (not a nice-to-have)
- What the FDA expects when it comes to cybersecurity in your submission
- How to spot common security gaps before the FDA finds them
- Easy ways to build cybersecurity into your development process — even if you're starting late
- Tips to get through the FDA review process faster and with fewer headaches
Our team of FDA analysts and cybersecurity experts provide robust and actionable cybersecurity roadmaps to ensure you meet FDA requirements. Get the Medcrypt advantage today!
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