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Fast Facts

Monitoring Clinical Trials for GCP Compliance

Jul 21, 2008 - Jul 22, 2008
Regus Southampton, London, England, United Kingdom
 

Highlights

PTI's practical 2-day course gives a complete overview of the modern regulatory GCP framework and takes a detailed look at roles and responsibilities in clinical trials. Delegates will take part in exercises demonstrating how to set up a trial site, make the best use of monitoring visits, and detect inconsistencies using documentation and available data. Participants will also learn how to deal with adverse event reporting quickly and efficiently to avoid non-compliance.

Event Profiles

Speakers: Mark Turkish (training for industry porfessionals, Education Training and Development)

Contact Details

Contact person: Customer Services - PTI
Email address:
Event website: http://www.iir-events.com/IIR-conf/PTI/EventView.aspx?EventID=191
Phone: +44 (0)20 7017 7481

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