European Legislation for Clinical Research - Implementation in Belgium

European Centre for Clinical Research Training (ECCRT)
Archivio
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13.11.2014  Brussels, Belgium
 
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26.02.2015  Brussels, Belgium
 
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30.11.2015  Brussels, Belgium
 
Contenuti (corsi)
This 3.5-hour programme focuses on the legal requirements of performing clinical trials with medicinal products in Belgium.

The Belgian law of 7 May 2004 on experiments on humans, implementing the European directive 2001/20/EC. A number of Royal Decrees and circular letters have also been published, which detail the practical implementation of the law. Including illustrations and practical examples to help participants understand how these Directives should be implemented.
Obiettivi didattici, obiettivi del training
To provide an overview of the implementation of the EU directive into Belgian law
Pubblico target
Everyone involved in clinical research, including: pharmaceutical companies, contract research organisations, investigators, site personnel and ethics committee members.
Opportunità di lavoro e di formazione specialistiche per post-laureati
CRA, Clinical Research Associate, PM, Project Manager
Certificazioni
ISO9001:2008/ Q-for
Organizzatori regionali
ECCRT
 

Informazioni ed Iscrizioni:

Ms. Sunita Kelecom
 
Categorie
Ricerca clinica
Contatto organizzatori
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
 
"Noi, Going International, siamo un’azienda che si è scelta come obiettivo di rendere acessibile la formazione a una grandissima quantità di persone, oltrepassanddo i confini geografici e sociali."

AMREF - African Medical and Research FoundationOÖ Gebietskrankenkasse, Referat für Wissenschaftskooperation Swiss Tropical and Public Health InstitutenewTreeHilfswerk AustriaÄrzte der WeltAGEM - Arbeitsgemeinschaft Ethnologie und MedizinEuropean Public Health Association (EUPHA)