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Therapeutic Innovation & Regulatory Science|August 10, 2023
Global Postmarket Pharmacovigilance: A Generic Drug PerspectiveTaylor Dalsey, Edward Kim, Howard Chazin, et al.Therapeutic Innovation & Regulatory Science|June 20, 2020
FDA's Generic Drug Program: Decreasing Time to Approval and Number of Review CyclesHoward Chazin, Jason Woo, Jing Han, et al.Therapeutic Innovation & Regulatory Science|October 27, 2018
Abbreviated New Drug Applications: Generic Drug User Fee Amendments Act Analysis of Application Quality MetricsJason Woo, Jingyu Julia Luan, Zili Li, et al.Pageof 1