1.
Clin Pharmacol Ther
; 94(2): 230-42, 2013 Aug.
Artículo
en Inglés
| MEDLINE
| ID: mdl-23588316
RESUMEN
Globalization of clinical research has led to an increase in clinical trials conducted outside of the United States that are submitted to the US Food and Drug Administration (FDA) in new drug applications. This article discusses the FDA's experience with these submissions in specific therapeutic areas, including the extent of this practice, differences between the effectiveness and safety outcomes of studies conducted inside and outside the United States, and the FDA's approach to acceptance of these trials.