Abernethy: Core FDA priorities will be evidence generation, personalized medicine, drug design
Dr. Amy Abernethy · a16z Podcast | Connecting Hearts, Bodies, and Networks to Cure Cancer · Feb 26, 2019 · at 35:00
Dr. Amy Abernethy, incoming Principal Deputy Commissioner at the U.S. Food and Drug Administration (FDA), discusses her focus areas upon stepping into her regulatory role.
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“When I'm at FDA, I will have a trans-FDA remit, so I will need to spend my time and energy working on the things that the FDA needs me to do, and I'm looking forward to learning more and more about that every day. But I know that I'll at least spend some of my personal extra energy on three core areas, one being accelerating evidence generation. I can't work with One Health anymore, but you can sort of hopefully see how I've been thinking about evidence generation for a long time. The second is as it relates to personalized medicine. This has been a core focus for me for a long time as an oncologist, and that's just as a person. And then the third is patient-informed drug design.”
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