SEMINARIO DE CAPACITACIÓN
Buenas Prácticas en Investigaciones Clínicas en Medicamentos
Organiza: Biodiseq – Hospital Israelita
Fecha: jueves 11 de diciembre de 2008 - 17 hs a 20.30 hs
Sede
Hospital Israelita
Av. Nazca 1450 – Ciudad de Buenos Aires
Programa analítico: Desarrollo de drogas . Fases de investigación en medicamentos-Aspectos éticos y Regulatorios nacionales e internacionales en investigación clinica farmacológica. – Aspectos éticos y Regulatorios nacionales e Internacionales en investigación Farmacológica
16:30 hs Acreditación
17:00 hs Apertura del Seminario a cargo de el Dr. Marcos Panzuto (Htal.Israelita)
17:15 hs Desarrollo de drogas. Fases de investigación en medicamentos
17:45 hs Aspectos éticos y Regulatorios nacionales e Internacionales en Investigación clínica farmacológica
18.30 hs Intervalo
18-45 hs Responsabilidades de los investigadores y patrocinadores
19:30 hs Presente y futuro de la investigación clínica con medicamentos
20.15 hs Cierre del Seminario
Directores: Dra. Celeste Burrieza – Dra Liliana Vetere
Coordinadores: Dra. Celeste Burrieza – Sr. Jorge Pardo
Disertantes: Dr. Ezequiel KlimovsKy ( Director asociado Quid Consulting SRL)
Período de inscripción 1 / 10 de diciembre de 2008 – Arancel Profesional $80 , Estudiantes $35 , Personal del Hospital Israelita sin cargo. Inscripción previa
Certificación final: Se entregará Certificado de Asistencia
Informes e Inscripción
Tel 5235-3903 cel 15 5953 1392 e-mail celeste.burrieza@biodiseq.com.ar
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