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Drug Product Stability and Shelf-Life

 
  July 09, 2007  
     
 
The Center for Professional Advancement, Amsterdam
17-19 December 2007


Who Should Attend:
This course contains in-depth coverage of the science and practice of drug stability and shelf-life, and is designed to benefit the following personnel:

QC/QA Managers/Supervisors
Product Stability Managers
Manufacturing Personnel
Research & Product Development Scientists and Managers
Regulatory Personnel
Pharmaceutical Consultants


Description:
This course focuses on the science and principles concerning stability of pharmaceutical, biotechnology and cosmetic products. Kinetic approaches to chemical stability will be covered and the advantages and limitations of accelerated stability testing will be discussed. Degradation by chemical, physical and microbiological factors will be covered. Data analysis and practical aspects of stability such as the role of packaging in stability will be included. Considerable attention will be given to analytical methodology, data analysis and data management. Current FDA Stability guidelines and ICH Guidelines on stability will be discussed. The course includes a workshop for hands-on experience of data and statistical analysis.

 
 
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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