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Essentials of Clinical Study Management

June 20, 2008

Drug Information Association, SAS Radisson Hotel Boulogne, Paris, France. Sep 22 2008 The success of a clinical study is very much dependant on its efficient preparation and effective conduct. Study managers should be knowledgable about required quality and regulatory standards, roles and responsibilities of team members and be able to select and oversee internal and external resources. Study managers also should be able to anticipate potential problems, offer creative solutions and develop strategies to mitigate risk. This training course provides a comprehensive overview of the essential elements of study management and the clinical study environment in the context of the overall drug development process.After successful completion of the training course the participants will be able to efficiently plan, execute and manage a clinical study from protocol to final report.

Organized by:			Drug Information Association
Invited Speakers:			Patricia Fitzgerald Managing Director Adamas Consulting Ltd. United Kingdom. Paivi Itkonen Managing Director Crown CRO Oy Finland. Jennifer A Kealy Managing Director Cascade Clinical Consulting Ltd. France. Ingrid Klingmann, Dr. Med, MD President Pharmaplex bvba Belgium. Deborah Malins Russell QA Services United Kingdom. Tamara Schaerer Managing Director SRS Schaerer Research Services Switzerland.

Deadline for Abstracts:			-

Registration:			http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=16881&eventType=Training Course
E-mail:			talana.bertschi@diaeurope.org

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