Review paper
Generating comparative evidence on new drugs and devices after approval
Abstract
Certain limitations of evidence available on drugs and devices at the time of market approval often persist in the post-marketing period. Often, post-marketing research landscape is fragmented. When regulatory agencies require pharmaceutical and device manufacturers to conduct studies in the post-marketing period, these studies might remain incomplete many years after approval. Even when completed, many post-marketing studies lack meaningful...
Paper Details
Title
Generating comparative evidence on new drugs and devices after approval
Published Date
Mar 1, 2020
Journal
Volume
395
Issue
10228
Pages
998 - 1010
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