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Good Clinical Practices (GCPs)

 
  October 18, 2012  
     
 
Center for Professional Innovation & Education, Inc., Berlin, Germany
Mar 18 - 20, 2013


This is a three-day course designed to provide individuals with an in-depth understanding of the clinical research process, the roles and responsibilities of key players, as well as, regulatory requirements.  The course consists of lecture and exercises designed to focus on the practical implementation of the GCP requirements.   Participants will also be placed in several real life situations such as reviewing pre-study documents and informed consent form for completeness and compliance; conducting drug accountability; reviewing case report form for accuracy and adherence to protocol and performing source document verification.
 
 
Organized by: Center for Professional Innovation & Education, Inc.
Invited Speakers: Contact info@cfpie.com for a list of course instructors
 
Deadline for Abstracts: n/a
 
Registration: http://www.cfpie.com/showitem.aspx?productid=039&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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