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European Legislation for Clinical Research - Implementation in Belgium

European Centre for Clinical Research Training (ECCRT)

Archivo

13.11.2014 Brussels, Belgium

26.02.2015 Brussels, Belgium

30.11.2015 Brussels, Belgium

Contenido de curso
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.

Objetivos de formación
To provide an overview of the implementation of the EU directive into Belgian law

Destinatario
Everyone involved in clinical research, including: pharmaceutical companies, contract research organisations, investigators, site personnel and ethics committee members.

Oportunidad de trabajos y los campos profesionales mas buscados por personas ya tituladas
CRA, Clinical Research Associate, PM, Project Manager

Certificación
ISO9001:2008/ Q-for

Organizador local
ECCRT

Información e inscripción:

Ms. Sunita Kelecom