European Legislation for Clinical Research - Implementation in Belgium

European Centre for Clinical Research Training (ECCRT)
Archive
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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
 
Course Content
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.
Learning objectives, training objectives
To provide an overview of the implementation of the EU directive into Belgian law
Target Audience
Everyone involved in clinical research, including: pharmaceutical companies, contract research organisations, investigators, site personnel and ethics committee members.
Typical postgraduate careers and job opportunities
CRA, Clinical Research Associate, PM, Project Manager
Certifications
ISO9001:2008/ Q-for
Local Organizer
ECCRT
 

Enquiries and Registration:

Ms. Sunita Kelecom
 
Categories
Clinical Research
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
 
"Going International promotes access to education and training for all regardless of social, geographic and national borders."

Swiss Tropical and Public Health InstituteOÖ Gebietskrankenkasse, Referat für Wissenschaftskooperation European Public Health Association (EUPHA)Anästhesie in Entwicklungsländern e. V.Center of ExcellenceCharité International AcademyÄrzte der WeltEuropean Health Forum Gastein