Understanding the European Legislation & Implementing the Guidelines
European Centre for Clinical Research Training (ECCRT)
Archivo
29.01.2015 Brussels, Belgium
07.05.2015 Brussels, Belgium
08.09.2015 - 08.10.2015 Brussels, Belgium
26.11.2015 Brussels, Belgium
Contenido de curso
This 1-day course is designed to provide understanding of the European Clinical Trials Directives 2001/20/EC and 2005/28/EC. The state-of-the-art regarding implementation and implications in the European member states will be presented. Other topics are the latest developments regarding safety reporting and applications of the European Databases. Interactive presentations are intended to better understand the implementation of requirements and guidance documents.
This 1-day course is designed to provide understanding of the European Clinical Trials Directives 2001/20/EC and 2005/28/EC. The state-of-the-art regarding implementation and implications in the European member states will be presented. Other topics are the latest developments regarding safety reporting and applications of the European Databases. Interactive presentations are intended to better understand the implementation of requirements and guidance documents.
Objetivos de formación
Understand the European directives. Comprehend the implementation in the EU. Know the procedures to be compliant and reach successful implementation.
Understand the European directives. Comprehend the implementation in the EU. Know the procedures to be compliant and reach successful implementation.
Destinatario
Everyone involved in clinical research including: pharmaceutical companies, contract research organisations, investigators, site personnel, ethics committee members, etc.
Everyone involved in clinical research including: pharmaceutical companies, contract research organisations, investigators, site personnel, ethics committee members, etc.
Oportunidad de trabajos y los campos profesionales mas buscados por personas ya tituladas
CRA, Clnical research Associate, PM, Project Manager
CRA, Clnical research Associate, PM, Project Manager
Certificación
ISO9001:2008/ Q-for
ISO9001:2008/ Q-for
Organizador local
ECCRT
ECCRT
Información e inscripción:
Ms. Sunita Kelecom
Investigación clínica
Idioma
Inglés
Inglés
Costos
EUR 750,00
EUR 750,00
Cantacto organizador
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
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