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Drug Information Association, Four Points by Sheraton Elysee Palace Hotel, Nice, France
Feb 6 2008
The success of a clinical study is very much dependant on its efficient preparation and conduct. Staff involved should be knowledgable about roles and responsibilities of team members, creation of management tools, required quality and regulatory standards. Study managers also should be able to anticipate potential problems and come up with creative solutions. This training course provides a comprehensive overview over all elements of study management, the clinical study environment and the overall drug development process. After successful completion of the training course the participants will be able to prepare and manage a clinical study from protocol to final report.
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Organized by:
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Drug Information Association |
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Invited Speakers:
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1) Ingrid Klingmann (Course Director)Managing Director, Pharmaplex BVBA, Belgium 2) Patricia FitzgeraldManaging Director, Adamas Consulting, UK 3) Päivi ItkonenManaging Director, Crown CRO Oy, Finland 4) Jennifer KealyManaging Director, Cascade Clinical Consulting,France 5) Deborah MalinsGCP QA Consultant, Russell QA Services, UK 6)Tamara Schärer Managing Director, SRS Schärer Research Services,Switzerland.
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Deadline for Abstracts:
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-
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Registration:
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http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=15270&eventType=Training%20Course
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E-mail:
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diaeurope@diaeurope.org
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