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Excipient GMPs

 
  June 22, 2007  
     
 
The Center for Professional Advancement, New Brunswick, NJ
July 16-18, 2007


Who Should Attend: This course is intended for chemical manufacturers who want to learn about supplying excipients to the industry and for those manufacturers already supplying excipients that need to learn about excipient GMP compliance. It is also intended for pharmaceutical manufacturers that must assess the compliance of their excipient suppliers to appropriate GMP requirements.

Personnel in the following areas have found this course beneficial:

Quality Assurance
Quality Control
Regulatory Affairs
Quality Audit
New Business Development



Description: This course will cover the regulatory, quality, and manufacturing issues involved in providing chemicals for use as excipients (inactive ingredients) in the manufacture of drug products. You will learn about the regulation of chemicals sold for use as excipients by the FDA, the expectations of the pharmaceutical industry, and excipient quality system requirements (GMP). There will also be topical information on current issues facing the industry.


Course Type: A Three Day Intensive Course

 
 
Organized by: The Center for Professional Advancement
Invited Speakers: Please click here for speaker information.
 
Deadline for Abstracts: not applicable
 
Registration: Please click here for registration information.
E-mail: info@cfpa.com
 
   
 
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