ISO 14155 training for CRAs
European Centre for Clinical Research Training (ECCRT)
Archiv
22.05.2014 Brussels, Belgien
Kursinhalte
You are a monitor who needs to understand the counterpart of ICH-GCP for medical device trials. You want to know the rules and responsibilities outlined in ISO14155 and get some practical advice and hints and tips on improving your monitoring skills? This course is made for you and your colleagues!
You are a monitor who needs to understand the counterpart of ICH-GCP for medical device trials. You want to know the rules and responsibilities outlined in ISO14155 and get some practical advice and hints and tips on improving your monitoring skills? This course is made for you and your colleagues!
Lernziele, Trainingsziele
To understand the role of clinical studies in the development of devices
To be familiar with the basic requirements on how clinical trials are carried out
To appreciate the device-specific study elements as compared to drugs studies
To understand the role of clinical studies in the development of devices
To be familiar with the basic requirements on how clinical trials are carried out
To appreciate the device-specific study elements as compared to drugs studies
Zielpublikum
Recently started CRAs or Investigators and study co-ordinators.
Recently started CRAs or Investigators and study co-ordinators.
Zertifizierung
ISO 9001:2008 / Q-for
ISO 9001:2008 / Q-for
Lokaler Veranstalter
European Centre for Clinical Research Training
European Centre for Clinical Research Training
Anfragen und Anmeldung:
Frau Sunita Kelecom
Klinische Forschung
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
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