In 2024, the FDA approved over a hundred AI-enabled medical devices, highlighting rapid innovation in healthcare technology. The FDA also introduced fresh draft guidelines emphasizing continuous validation, lifecycle management, and tighter cybersecurity protocols. Discover how these medical device design standards impact device manufacturers and what steps must be taken now to ensure compliance and patient safety. 

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When it comes to atrial fibrillation treatments, cryoablation vs radiofrequency ablation is a common comparison. In this episode, we’ll break down both methods, highlighting their similarities, differences, and unique applications.

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Pulsed field ablation vs. radiofrequency ablation is an increasingly common comparison among medical practitioners when selecting which to use for treating patients. Find out why in this episode where we discuss these two treatment types.

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Bringing a new concept through the development process and to market is no small feat. That's why understanding the FDA-regulated steps to gain approval and how that is implemented during the medical device product development process, is crucial. Learn the ins and outs of what the FDA requires in our helpful podcast.

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Turning an idea for innovation into a useful, safe, and profitable medical device is an impressive feat. Learn how a go-to-market strategy for medical devices is pivotal for turning a good idea into an impressive product in Vantage MedTech's insightful podcast.

Read more here: https://vantagemedtech.com/medical-device-go-to-market-strategy Connect with us: https://www.linkedin.com/company/vantage-medtech/ https://www.youtube.com/@VantageMedTech Learn more about Vantage MedTech: https://vantagemedtech.com/