Understanding the European Legislation & Implementing the Guidelines
European Centre for Clinical Research Training (ECCRT)
Archiv
29.01.2015 Brussels, Belgien
07.05.2015 Brussels, Belgien
08.09.2015 - 08.10.2015 Brussels, Belgien
26.11.2015 Brussels, Belgien
Kursinhalte
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.
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.
Lernziele, Trainingsziele
Understand the European directives. Comprehend the implementation in the EU. Know the procedures to be compliant and reach successful implementation.
Understand the European directives. Comprehend the implementation in the EU. Know the procedures to be compliant and reach successful implementation.
Zielpublikum
Everyone involved in clinical research including: pharmaceutical companies, contract research organisations, investigators, site personnel, ethics committee members, etc.
Everyone involved in clinical research including: pharmaceutical companies, contract research organisations, investigators, site personnel, ethics committee members, etc.
Typische Postgraduate Berufsfelder und Berufschancen
CRA, Clnical research Associate, PM, Project Manager
CRA, Clnical research Associate, PM, Project Manager
Zertifizierung
ISO9001:2008/ Q-for
ISO9001:2008/ Q-for
Lokaler Veranstalter
ECCRT
ECCRT
Anfragen und Anmeldung:
Frau Sunita Kelecom
Klinische Forschung
Sprache
Englisch
Englisch
Kosten
EUR 750,00
EUR 750,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
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