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European Legislation for Clinical Research - Implementation in Belgium

European Centre for Clinical Research Training (ECCRT)
Archiv
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13.11.2014  Brussels, Belgien
 
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26.02.2015  Brussels, Belgien
 
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30.11.2015  Brussels, Belgien
 
Kursinhalte
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.
Lernziele, Trainingsziele
To provide an overview of the implementation of the EU directive into Belgian law
Zielpublikum
Everyone involved in clinical research, including: pharmaceutical companies, contract research organisations, investigators, site personnel and ethics committee members.
Typische Postgraduate Berufsfelder und Berufschancen
CRA, Clinical Research Associate, PM, Project Manager
Zertifizierung
ISO9001:2008/ Q-for
Lokaler Veranstalter
ECCRT
 

Anfragen und Anmeldung:

Frau Sunita Kelecom
 
Kategorien
Klinische Forschung
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
 
"GOING INTERNATIONAL fördert den Zugang zu Aus-, Fort- und Weiterbildung, unabhängig von sozialen, geographischen und nationalen Grenzen."

Österreichisches Rotes KreuzOÖ Gebietskrankenkasse, Referat für Wissenschaftskooperation European Public Health Association (EUPHA)AGEM - Arbeitsgemeinschaft Ethnologie und MedizinAlumni Club Medizinische Universität WiennewTreeÖsterreichische Akademie der ÄrzteCenter of Excellence