mail
Druckansicht
 
 

Good Manufacturing Practice (GMP) in relation to GCP

European Centre for Clinical Research Training (ECCRT)
Archiv
-
30.10.2015  Brussels, Belgien
 
Kursinhalte
This one day course is designed for professionals who are involved in the handling of investigational medicinal products. They will get an overview of the latest regulatory standards set by the European Union including Directive 2001/20/EC, 2003/94/EC, 2005/28/EC, Annex 13 of EC-GMP Guideline, ICH GMP Q7 and ICH GCP E6 guidelines.
Lernziele, Trainingsziele
To give a comprehensive overview of the different regulatory references regulating GMP requirements for investigational medicinal products.
To explain steps, roles and responsibilities in the course of IMP manufacturing and processing.
Zielpublikum
Monitors, project managers, site personnel, or administrative persons who are responsible for sending, storing, accountability, final disposition, etc of medicinal products used in clinical trials.
Zertifizierung
ISO 9001:2008/ Q-for
 

Anfragen und Anmeldung:

Frau Sunita Kelecom
 
Kategorien
Klinische Forschung
Dauer
1 Tag
Sprache
Englisch
Kosten
EUR 850,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
 
"GOING INTERNATIONAL fördert den Zugang zu Aus-, Fort- und Weiterbildung, unabhängig von sozialen, geographischen und nationalen Grenzen."

Österreichische Akademie der ÄrzteAGEM - Arbeitsgemeinschaft Ethnologie und MedizinCentro per la Formazione Permanente e l'Aggiornamento del Personale del Servizio SanitarioHelix - Forschung & Beratung WienOÖ Gebietskrankenkasse, Referat für Wissenschaftskooperation Swiss Tropical and Public Health InstituteAMREF - African Medical and Research FoundationÖsterreichisches Rotes Kreuz