Califf: More Expedited Approvals Mean US Clearance Only The Beginning Of Learning About Medical Products

The US FDA commissioner said increased use of expedited approval pathways will help spur clinical research system reform.

Califf speaks to DIA
FDA Commissioner Robert Califf spoke at the DIA Global Annual Meeting in Chicago via video. • Source: Derrick Gingery

CHICAGO – Robert Califf expects sponsors likely will have to adapt development programs to the level of evidence available upon marketing clearance if expedited pathways become even more of the norm.

Califf, US Food and Drug Administration Commissioner, envisions pre-approval development as only the

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