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No. 0 Policy & regulation

Dr. Michelle Tarver, MD, PhD

Director, Center for Devices and Radiological Health, US Food and Drug Administration • United States

Leads the FDA centre that reviews every medical device and clinical AI product seeking the US market.

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The Signal

Tarver directs the FDA device centre at the moment AI-enabled devices, predetermined change control plans and new payment pathways are reshaping how digital health products reach patients, making her decisions central to the sector.

Who Dr. Michelle Tarver, MD, PhD is

Leads the FDA centre that reviews every medical device and clinical AI product seeking the US market.

Tarver directs the FDA device centre at the moment AI-enabled devices, predetermined change control plans and new payment pathways are reshaping how digital health products reach patients, making her decisions central to the sector.

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At a glance

Role
Director, Center for Devices and Radiological Health
Organisation
US Food and Drug Administration
Platforms
LinkedIn
Based in
United States, North America
Influence Score 84.1editorial estimate, see how it is built
Reach (25% weight)70

Audience size across LinkedIn, X, YouTube, podcasts and newsletters.

Engagement (20% weight)66

How much the audience actually reacts, comments, shares and subscribes.

Credibility (25% weight)97

Clinical, research, operating or investing track record behind the commentary.

Consistency (15% weight)70

Publishing cadence and how reliably they show up with original work.

Industry impact (15% weight)96

Whether decision makers, policy and capital actually move on what they say.

Scores are subjective editorial estimates compiled by our research desk from public profiles and published work. They are opinion, not measurement, and they are not a judgement of any person's character or ability.

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