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Drug Information Association, Auditorium Madrid Hotel, Avenida de Aragon, 400, Madrid, Spain
Oct 18 2007
As setting up and running clinical trials is now a complex and highly pressurised process, it is essential that clinical research proffessionals have the technical and the interpersonal skills to run clinical trials on time, to meet the increasing demands of regulatory quality requirements and to budget. As the nature of clinical research projects have requirements and issues particular to them, this course has been designed specifically for clinical research proffessionals and will be delivered by an expert in clinical research project management. This highly interactive course will give you practical project management tools and techniques to ensure that your clinical research projects are a success.
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Organized by:
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Drug Information Association |
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Invited Speakers:
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Laura Brown Course Director, MSc. Clinical Research, School of Pharmacy, University of Cardiff and Independent QA and Training Consultant.
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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=14389&eventType=Training%20Course
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E-mail:
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diaeurope@diaeurope.org
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