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Unpacking FDA Guidance: Quality System Considerations and Content of Premarket Submissions

Topics:
FDA readiness, Regulatory, Thought leadership
Unpacking FDA Guidance: Quality System Considerations and Content of Premarket Submissions
Unpacking FDA Guidance: Quality System Considerations and Content of Premarket Submissions
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October 12, 2023
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What do medical device manufacturers need to understand about the final guidance, "Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions."the guidance? Join the free webinar to hear from MedCrypt’s FDA experts Naomi Schwartz and Seth Carmody in a conversation lead by CEO Mike Kijewski.

Speakers

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!

Naomi Schwartz

Naomi Schwartz

Sr Director of Cybersecurity Quality and Safety
Seth Carmody

Seth Carmody

VP of Regulatory Strategy
Mike Kijewski

Mike Kijewski

CEO

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