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New Opportunities, New Challenges: FDA Elaborates on use of Digital Health in Drug and Biological Product Development
This is Part 1 in a series of blog posts on developments from the U.S. Food and Drug Administration (“FDA”) regarding its commitments set forth under the Prescription Drug Under Fee Act.
Reed smith
Steering committee
Drug development tool qualification program
Drug administration
Duke margolis center
Product development
Digital health technologies framework
Clinical trial diversity
Drug omnibus reform act
President biden
Trial diversity
Prescription drug user fee act
Digital health technologies
Biological product development
Remote data acquisition
Clinical investigations
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