Clinical Research Training for Investigators

European Centre for Clinical Research Training (ECCRT)
Archivio
-
08.10.2014  Brussels, Belgium
 
Contenuti (corsi)
Investigators are trainer on their specific duties within Clinical Research. In 1 day, they get to understand the regulations, GCP guidelines and their responisbilities with regards to safety reporting and informed consent. Participants will receive a GCP certificate showing their capacity to work according to the current laws and regulations.
Obiettivi didattici, obiettivi del training
To know everything about current clinical practice
To understand the responsabilities of a Medical Doctor withing Clinical Trials
To fully comprehend the safety reporting procedure
To be able to get a voluntary and understandable informed consent
Pubblico target
Medical Doctors looking to participate in Clinical Trials. Investigators conducting Clinical Research.
Certificazioni
ISO 9001:2008 / Q-for
Organizzatori regionali
European Centre for Clinical Research Training
 

Informazioni ed Iscrizioni:

Ms. Sunita Kelecom
 
Categorie
Ricerca clinica
Durata
1 giorno
Lingua
Inglese
Costi
EUR 1.250,00
Contatto organizzatori
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
 
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