Navigating the cybersecurity landscape for medical devices requires an understanding of both European Union (EU) and US Food and Drug Administration (FDA) guidance. Ensuring your teams can execute efficiently and meet the distinct yet often overlapping requirements can be a significant undertaking.
Building on our previous joint webinar "Bridging the Gap: Navigating EU and US Medical Device Cybersecurity Regulations", Axel Wirth, Chief Security Strategist of Medcrypt, and Christian Rosenzweig, Medical Device Consultant at the Johner Institut will be providing a deep dive into select cybersecurity topics. Our webinar on Wednesday, June 25th, is designed to equip you with the knowledge and strategies to align with EU and FDA medical device cybersecurity expectations in general and select pre- and post-market topics in specific. Learn how to comply with essential cybersecurity principles and practices relevant to both EU and the FDA regulatory environments.
Don't let the complexities of dual regulatory requirements hinder your progress. Register now and learn how to train your team effectively and efficiently.
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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