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Regulatory Affairs Part I: The IND Phase

 
  February 20, 2011  
     
 
McCormick Place, Chicago, IL
Jun 17 2011 10:30AM - Jun 19 2011 11:45AM


All You Need to know about IND Submissions in Only 3 Days

 

Learn how to apply regulatory concepts to ensure compliant IND submissions to FDA. The course focuses on drug and well characterized biological products and not the regulatory process for devices, generic products, or traditional biologics.

 

Event Code:
11433

 

 
 
Organized by: DIA
Invited Speakers: See website for speaker information
 
Deadline for Abstracts: Call contact
 
Registration:
For detailed program information including faculty and topics, please contact:
Susan Mazak
Tel. +1-215-442-6183

E-mail: susan.mazak@diahome.org
 
   
 
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