European Legislation for Clinical Research - Implementation in 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

Ms. Sunita Kelecom