• Pharmaceutical Supply Chain Integrity - What Needs to be Done and Where!

Featuring presentations by: an excipient manufacturer, a distributor, a pharmaceutical finished product manufacturer, and FDA - plus - a U.S. Customs Official.

• The Excipient Qualification Process - Next Steps

What constitutes an "Excipient Pedigree": necessary elements of a comprehensive Quality Agreement and the supplier-user negotiation process.

• Implementation of IPEC's Excipient Information Package (EIP) -
  It's Current Status and What Lies Ahead

Reports from excipient manufacturers, supplier distributors, and users.

• A Case for a Global Excipient Forum!

Presentations by international spokespersons representing industry segments, the pharmacopeias, and regulatory authorities.

• Current Issues Relating to Excipient Functionality
  and Performance - How Both Fit into Quality by Design
  
  
• Pharmaceutical Development Today - Why Novel Co-Processed Excipients are Essential!
  
  
  Registration now available!
  
  Registration Fees:
  $795 IPEC-Americas member company employees
  $895 Non-member
  $150 Government/Academic
  $50 Student

  
  
  

  
  

If you need immediate information, please contact:

Kim Beals
Executive Director
(703) 875-8712

.