Sistema de Información Esencial en Terapéutica y Salud

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Última actualización: 24/6/2019
SIETES contiene 92761 citas

 
 
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Wallach JD, Eqilman AC, Dhruva SS, McCarthy ME, Miller JE, Woloshin S, Schwartz LM, Ross JS. Postmarket studies required by the US Food and Drug Administration for new drugs and biologics approved between 2009 and 2012: cross sectional analysis. BMJ 2018;361:24 de mayo. [Ref.ID 102886]
2. Cita con resumen
Redberg RF, Gartenberg AJ, Peleg A, Dhruva SS. Presumed safe no more: lessons from the Wingspan saga on device regulation. BMJ 2014;348:g93. [Ref.ID 97246]
3. Cita con resumen
Dhruva SS, Redberg RF. Accelerated approval and possible withdrawal of midodrine. JAMA 2010;304:2172-3. [Ref.ID 89668]
4. Cita con resumen
Dhruva SS, Bero LA, Redberg RF. Strenght of study evidence examined by the FDA in premarket approval of cardiovascular devices. JAMA 2009;302:2679-85. [Ref.ID 87398]
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