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Good Laboratory Practices for Pre-Clinical Testing

 
  May 04, 2012  
     
 
Center for Professional Innovation & Education, Inc., King of Prussia, PA
Nov. 1 & 2


This two-day Good Laboratory Practices (GLP) course is designed for all scientists (managerial and laboratory), regulatory affairs and compliance personnel who are active in pre-clinical studies and in other laboratory settings.  It will be of most benefit to professionals whose job function necessitates the generation, evaluation, assurance and submission of data from pre-clinical studies.  Principal Investigators, Study Directors, Study Monitors and professionals aspiring to these positions will derive benefit from the course.
Attendees will develop a strong foundation for compliance requirements for current Good Laboratory Practices, and will be able to apply compliance protocols in all efforts aimed at generating regulated data for evaluation by the US FDA and regulatory agencies overseas.  All participants will gain a fundamental understanding of the basis of the regulations and the necessity of rigorous implementation.  Special attention will be given to incorporating proactive thinking and a robust compliance regimen in all scientific matters. The consequences of non-compliance will be examined, including a thorough review of examples of previous FDA inspectional findings. 
 
 
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=112&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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