Understanding the European Legislation & Implementing the Guidelines

European Centre for Clinical Research Training (ECCRT)
Archive
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29.01.2015  Brussels, Belgium
 
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07.05.2015  Brussels, Belgium
 
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08.09.2015 - 08.10.2015  Brussels, Belgium
 
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26.11.2015  Brussels, Belgium
 
Course Content
This 1-day course is designed to provide understanding of the European Clinical Trials Directives 2001/20/EC and 2005/28/EC. The state-of-the-art regarding implementation and implications in the European member states will be presented. Other topics are the latest developments regarding safety reporting and applications of the European Databases. Interactive presentations are intended to better understand the implementation of requirements and guidance documents.
Learning objectives, training objectives
Understand the European directives. Comprehend the implementation in the EU. Know the procedures to be compliant and reach successful implementation.
Target Audience
Everyone involved in clinical research including: pharmaceutical companies, contract research organisations, investigators, site personnel, ethics committee members, etc.
Typical postgraduate careers and job opportunities
CRA, Clnical 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."

newTreeÄrztekammer für WienCentro per la Formazione Permanente e l'Aggiornamento del Personale del Servizio SanitarioEuropean Health Forum GasteinAGEM - Arbeitsgemeinschaft Ethnologie und MedizinÖsterreichische Akademie der ÄrzteEuropean Public Health Association (EUPHA)Österreichisches Rotes Kreuz