Drug Safety and Clinical Trials - A Concise Workshop
European Centre for Clinical Research Training (ECCRT)
Archiv
28.04.2011 Brussels
Kursinhalte
This foundational one day course on the essential aspects of clinical safety is designed for everyone involved in clinical research activities.
This course provides key definitions based on the new European Community legislation as well as on consensus forums such as ICH and the CIOMS Working Groups. Practical examples and workshops are intended to illustrate these definitions and introduce the skills needed to perform clinical safety tasks successfully.
This foundational one day course on the essential aspects of clinical safety is designed for everyone involved in clinical research activities.
This course provides key definitions based on the new European Community legislation as well as on consensus forums such as ICH and the CIOMS Working Groups. Practical examples and workshops are intended to illustrate these definitions and introduce the skills needed to perform clinical safety tasks successfully.
Lernziele, Trainingsziele
Identify key definitions and vocabulary used in clinical safety in the EU. Recognise important aspects in evaluating adverse events. Identify main characteristics of adverse events, etc.
Identify key definitions and vocabulary used in clinical safety in the EU. Recognise important aspects in evaluating adverse events. Identify main characteristics of adverse events, etc.
Zielpublikum
Project Managers, CRAs & CTAs responsible for clinical operations, drug safety personnel, investigators, representatives of organisations including academia running clinical trials and medical managers from the pharmaceutical industry.
Project Managers, CRAs & CTAs responsible for clinical operations, drug safety personnel, investigators, representatives of organisations including academia running clinical trials and medical managers from the pharmaceutical industry.
Typische Postgraduate Berufsfelder und Berufschancen
CRA, Clinical Research Associate, PM, Project Manager, Regulatory, Pharmacovigilance
CRA, Clinical Research Associate, PM, Project Manager, Regulatory, Pharmacovigilance
Zertifizierung
ISO9001:2008
ISO9001:2008
Lokaler Veranstalter
ECCRT
ECCRT
Anfragen und Anmeldung:
Frau Sunita Kelecom
Klinische Forschung
Sprache
Englisch
Englisch
Kosten
EUR 1.000,00
EUR 1.000,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
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