Deputy Director, Office of Cardiovascular Devices
FDA
Silver Spring, Maryland, United States
Misti Malone, Ph.D., is the Assistant Director of the Peripheral Interventional Devices Team in the Office of Cardiovascular Devices at FDA. As the Assistant Director, her primary responsibilities involve regulatory oversight of peripheral vascular devices across the total product life cycle, including submission review and supporting internal and external partnerships to bolster efficient device evaluation. She is actively involved in collaborations related to collection of global clinical evidence and real-world evidence to support clinical and regulatory decision-making as part of RAPID (a multi-stakeholder registry collaborative), the US-Japan Harmonization By Doing group promoting global regulatory solutions, and various other groups to support strategic priorities and FDA’s mission. She has authored several publications in various journals to share her group’s review perspectives.
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International Perspective From CDRH
Sunday, March 8, 2026
8:20 AM - 8:30 AM EST
INTERNATIONAL REGISTRY ARCHITECTURE TO ADVANCE REAL-WORLD EVIDENCE INFRASTRUCTURE
Sunday, March 8, 2026
9:55 AM - 11:20 AM EST
Panel Discussion | What Else is Needed to Demonstrate the Feasibility of Global Registries?
Sunday, March 8, 2026
10:35 AM - 11:20 AM EST
Sunday, March 8, 2026
12:00 PM - 12:35 PM EST
Panel Discussion | Future of Renal Denervation Studies and Clinical Implementation
Sunday, March 8, 2026
11:48 AM - 12:05 PM EST
Panel Discussion | From EFS to Real World Data
Tuesday, March 10, 2026
9:50 AM - 10:30 AM EST