Sistema de Información Esencial en Terapéutica y Salud

@SIETES7

Última actualización: 21/3/2019
SIETES contiene 92697 citas

 
 
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1. Cita con resumen
Silverman E. STAT Plus: AbbVie is sued for using Humira patent deals to block competition in the U.S.. STAT Daily Recap 2019:20 de marzo. [Ref.ID 103062]
2. Cita con resumen
Taylor P. GSK, J&J say monthly injection keeps HIV controlled. PMLiVE 2019:8 de marzo. [Ref.ID 103051]
4. Cita con resumen
Taylor P. Trump’s Brexit trade plan is bad for NHS, say campaigners. PMLiVE 2019:4 de marzo. [Ref.ID 103046]
5. Cita con resumen
Taylor P. Novartis back in the spotlight over Trump/Cohen links. PMLiVE 2019:28 de febrero. [Ref.ID 103043]
6.Enlace a cita original Cita con resumen
Hurley R. Medical cannabis: no NHS patients have benefited from law change, say campaigners. BMJ 2019;364:15 de febrero. [Ref.ID 103033]
7. Cita con resumen
8.Enlace a cita original Cita con resumen
Hadland SE, Rivera-Aguirre A, Marshall BDL, Cerdá M. Association of pharmaceutical industry marketing of opioid products with mortality from opioid-related overdoses. JAMA Network Open 2019;2:18 de enero. [Ref.ID 103009]
9. Cita con resumen
Thielking M. Federal trial over fentanyl bribes gets underway. STAT Morning Rounds 2019:2. [Ref.ID 103007]
11. Cita con resumen
Thielking M. PhRMA spent a record-breaking $27.5 million on lobbying in 2018. STAT Morning Rounds 2019:1. [Ref.ID 103004]
13. Cita con resumen
Anónimo. Sanofi, Regeneron revise immuno-oncology deal.. DIA Daily 2019:11. [Ref.ID 102998]
14. Cita con resumen
Anónimo. Eli Lilly to acquire Loxo Oncology for around $8 billion.. DIA Daily 2019:10. [Ref.ID 102997]
15. Cita con resumen
McConaghie A. BMS and Celgene announce $74bn merger. PMLiVE 2019:3 de enero. [Ref.ID 102993]
16. Cita con resumen
17. Cita con resumen
Healy D. The Goetzsche affair. Dr. David Healy (blog) 2018:5 de noviembre. [Ref.ID 102892]
18. Cita con resumen
Cooney E. Novartis unit teams up with medical marijuana producer, marking milestone for pharma. STAT Daily Recap 2018:18 de diciembre. [Ref.ID 102888]
19.Enlace a cita original Cita con resumen
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]
20.Enlace a cita originalTiene citas relacionadas Cita con resumen
Pacurariu A, Plueschke K, Olmo CA, Kurz X. Imposed registries within the European postmarketing surveillance system: Extended analysis and lessons learned for regulators. Pharmacoepidemiol Drug Saf 2018;27:julio. [Ref.ID 102879]
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