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This article was originally published in The Tan Sheet
Agenda for the panel's Jan. 11-12 meeting includes a discussion of issues related to in vitro dissolution testing of immediate-release and extended-release solid oral dosage forms and its relationship to in vivo bioavailability and bioequivalence. The meeting will begin at 8 a.m. on both days in conference rooms D & E of FDA's Parklawn Building
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