Asst Director, PIDT
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.
Disclosure information not submitted.
CRT 2024 | Faculty Assignment [FDA]
Saturday, March 9, 2024
9:00 AM – 9:00 PM ET
DISPARITIES IN PAD AND STRUCTURAL HEART
Sunday, March 10, 2024
3:10 PM – 12:00 AM ET
Disparities in CLTI Treatment and Outcomes
Sunday, March 10, 2024
3:42 PM – 3:50 PM ET
Sunday, March 10, 2024
3:58 PM – 4:13 PM ET
Moving Forward Hypertension Device Trial Design and Endpoints
Sunday, March 10, 2024
2:32 PM – 2:40 PM ET
Panel Discussion: How to Move Renal Denervation for Treatment of Hypertension in 2024
Sunday, March 10, 2024
3:12 PM – 3:27 PM ET