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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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February 05, 2012 |
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DIA, Horsham, PA USA
Mar 30 2012 8:00AM - 5:00PM
Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies. What You Will Learn · Roles and responsibilities of each member of the study team · Regulations and guidelines that govern clinical investigations · Informed consent elements and processes · Successful patient recruitment and retention strategies · Adverse event handling and reporting · Preparing for audits and audit process Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA. Event Code:
12412
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Organized by:
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DIA |
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Invited Speakers:
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Bernadette Ott
Consultant, Good Clinical Practices/Quality Assurance
United States
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Deadline for Abstracts:
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Call contact
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Registration:
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For registration questions, please contact Vicki Adkinson at (215) 4426162 or Vicki.Adkinson@diahome.org For agenda details, please contact Colleen Buckley at (215) 442-6108 or Colleen.Buckley@diahome.org
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E-mail:
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colleen.buckley@diahome.org
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