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SUSAR's in the EEA

  March 14, 2008  
Drug Information Association, Online
Apr 15 2008

Join us online for a 90 minute webinar to learn more about SUSAR Reporting for Interventional Clinical Trials in the EEA. WEBINAR HIGHLIGHTSIn 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.
Organized by: Drug Information Association
Invited Speakers: THOMAS STEINBACH, MD, PhD, FFPM (Dis) Qualified Person for Pharmacovigilance, SeniorDirector GSSELWyeth Europa Ltd., UK.
Deadline for Abstracts: -
Registration: http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=16993&eventType=Webinar
E-mail: dia@diahome.org
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