Document Type
Article
Publication Date
3-12-2024
Publication Title
BMJ Open
First Page
1
Last Page
12
DOI
doi:10.1136/ bmjopen-2023-076542
Abstract
Pharmaceutical innovation can contribute to reducing the burden of disease in human populations. This research asks whether products approved by the US Food and Drug Administration (FDA) from 2010 to 2019 and expedited review programmes incentivising development of products for serious disease were aligned with the US or global burden of disease.
Recommended Citation
Jackson, Matthew J.; Vaughan, Gregory; and Ledley, Fred D., 2024. Association Between Expedited Review Designations and the US or Global Burden of Disease for Drugs Approved by the US Food and Drug Administration, 2010–2019: A Cross-sectional Analysis, BMJ Open.
Included in
Pharmaceutics and Drug Design Commons, Pharmacy Administration, Policy and Regulation Commons