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FDA Publishes Groundbreaking AI/ML Medical Device Draft Guidance | Nelson Mullins Riley & Scarborough LLP
The U.S. Food and Drug Administration (“FDA”) has announced its first-ever draft guidance specifically addressing the use of artificial intelligence/machine learning (“AI/ML”) in.
White house
District of columbia
United states
Paul clowes
Nelson mullins
Patient engagement advisory committee meeting announcement oct
Drug administration
Nelson mullins riley scarborough
Nelson mullins riley
Drug omnibus reform act
Federal food
Cosmetic act
Predetermined change control plans
Draft guidance
Premarket approval
Implement device
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