ISACA Digital Videos
Experience ISACA through our lens. Explore our educational content, ISACA news and events, in-depth interviews with experts in cybersecurity, IT audit, governance and so much more, plus a link to ISACA’s audio podcast—all right here. Press play and you are on your way.
How the FDA and the Voluntary Improvement Program Support Continuous Improvement in MedTech
82 Views • 6 days ago
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Keisha Thomas, Associate Director for Compliance and Quality at FDA’s Center for Devices and Radiological Health, explains how the Voluntary Improvement Program (VIP) helps medical device organizations move beyond baseline compliance toward a stronger culture of quality, continuous improvement, and organizational innovation. In this conversation, she discusses why quality matters, how FDA supports VIP, what information the agency sees through the program, and how voluntary participation can create more collaborative, proactive relationships between industry and regulators. She also shares why companies on the fence should consider VIP as a practical way to strengthen capabilities, build trust, and invest in better outcomes for patients and the public.
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