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Clinical Trials Logistics & Supply Management

 
  September 01, 2009  
     
 
IQPC, Philadelphia, PA
December 7 – December 9, 2009


IQPC’s Clinical Trials Logistics & Supply conference will address key areas, including:

  • Complying with GMP requirements for global clinical trials
  • Minimizing risk through CTM production
  • Automating clinical trials labelling for improved efficiency and accuracy
  • Accurately forecasting clinical trial supply demands to reduce cost
  • Understanding CTS requirements for adaptive trials
  • Strategic partnerships & alliance management
  • Clinical tools, technology & systems for information management
  • Clinical trial productivity metrics & ROI
 
 
Organized by: IQPC
Invited Speakers: Who should attend? Clinical Supply Operations Clinical Trials Logistics Clinical/Investigational Supplies Shipping and Distribution Clinical Labeling / Packaging Clinical Trials Material Management Clinical Supplies Manufacturing Clinical Quality Assurance/Quality Control Regulatory Affairs Import-Export Trade Compliance Project Management Clinical Research / Planning Drug Supply Management
 
Deadline for Abstracts: no deadline
 
Registration:

Register online:

www.iqpc.com/Event.aspx?id=215922

Register by August 14th to attend for as low as $999

E-mail: info@iqpc.com
 
   
 
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