SUSARs in the EEA

Venue: Online

Location: Online, United States

Event Date/Time: Mar 14, 2008
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Description

Join us online for a 90 minute webinar to learn more about SUSAR Reporting for Interventional Clinical Trials in the EEA.

WEBINAR HIGHLIGHTS
In this webinar we will look at the following documents:
•Directive 2001/20/EC (alias Clinical Trials Directive and Good Clinical Practice Directive)

•Volume 10: Notice to Applicants. Special emphasis will be given in the areas of responsibilities of the sponsor, adverse event concept, reporting rules to EudraVigilance and prerequisites for reporting to EudraVigilance.

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