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Clinical Trial Inspections: Preparing for a good outcome

European Centre for Clinical Research Training (ECCRT)
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21.04.2015  Brussels, Belgien
 
Kursinhalte
This one day course is designed to provide a basic understanding of the inspection process - under special consideration of FDA inspections - in clinical drug development and will demonstrate the importance to ensuring good data quality, as a basis of successful inspection outcome.
Inspections are a fact of life when running clinical trials. This course will provide delegates with information about how inspections are conducted, advice on preparing for inspections and providing information to ins
Lernziele, Trainingsziele
Understand how inspections are conducted. Hands on information about how to prepare the team and documentation for a smooth inspection. Data and document requirements specific to inspections. Know how to prepare for sponsor/CRO and site inspections.
Zielpublikum
The course is developed for all staff who may be involved during an inspection, such as clinical operations staff, CRAs, project managers, investigators and their staff.
Typische Postgraduate Berufsfelder und Berufschancen
CRA, Clinical Research Associate, PM, Project Manager
Zertifizierung
ISO9001:2008/ Q-for
Lokaler Veranstalter
ECCRT
 

Anfragen und Anmeldung:

Frau Sunita Kelecom
 
Kategorien
Klinische Forschung
Art des Abschlusses
Teilnahmebescheinigung
Dauer
1 Tag
Sprache
Englisch
Kosten
EUR 850,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
 
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