Robert Califf, FDA's deputy commissioner for Medical Products and Tobacco, told attendees at the Drug Information Association annual meeting that the agency is trying to implement reforms to how it handles combination product submissions. The Gray Sheet caught up with Califf to ask him about the reforms. We spoke about that, data transparency and whether he'd consider taking on the role of FDA commissioner. Listen to our exclusive podcast or read the Q&A transcript below.
Califf, a cardiologist, joined FDA earlier this year, moving from his post as director of Duke University’s Translational Medicine Institute and vice chancellor for Clinical and Translational Research
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