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Pediatric Clinical Trial Design

 
  May 01, 2013  
     
 
Center for Professional Innovation & Education, Inc., Los Angeles, CA
Nov. 6 & 7, 2013


This course will review a process for closing the gap between regulatory requirements and study execution. Participants will acquire strategies for risk management in the areas of regulatory compliance, protocol execution and participant safety. Guidance documents important to pediatric research will be reviewed within the context of case studies from completed programs. Participants will be given an opportunity to share their experience during working sessions on protocol design and ethical issues.

In addition, there will be ample time to address specific problems and questions of individual participants.

 
 
Organized by: Center for Professional Innovation & Education
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=115&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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