Learn from comprehensive presentations by CDRH, industry representatives and regulatory experts
9:00 – 9:45 AM | Destination, Switzerland? The Impact of the Recent Decision of the Swiss Parliament on Medical Devices with FDA Authorization
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9:45 – 10:30 AM | Where We Are with MDR |
10:30 – 11:00 AM | FDA Priorities for 2023 |
11:00 – 11:20 AM | Recent Developments on the “Fraud on the FDA” Theory of False Claim Liability Rick Ball and Coleen Hill from Duane Morris will provide an overview of a theory of liability for pleading claims under the False Claims Act commonly referred to as “Fraud on the FDA.” They will discuss what risks such a theory might pose and delve into how various federal courts have recently accepted or rejected claims based on this theory. |
11:20 – 11:45 AM | Cybersecurity Best Practices for Regulated Medical Devices |
11:45 AM – 12:30 PM | Keynote Presentation & Q&A - Dr. Suzanne Schwartz, Director, Office of Strategic Partnerships and Technology Innovation, CDRH, FDA This session will provide an overview of the latest updates from CDRH’s Office of Strategic Partnerships and Technology, with a specific focus on digital health and cybersecurity. This briefing will be followed by a moderated Q&A session led by Amra Racic of Veeva Systems where you will get the chance to ask your questions directly to Dr. Schwartz! |
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