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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices

 
  March 26, 2012  
     
 
Center for Professional Innovation & Education (CfPIE), Los Angeles, CA
Aug. 27 - 29, 2012


This three-day course is designed for anyone who works in a current Good Manufacturing Practices (cGMP) environment, and anyone who needs to understand the concepts of cGMP and quality in a manufacturing setting.  Participants will gain a thorough understanding of cGMP regulations, as well as important ICH guidelines.  The latest techniques used to devise, implement and maintain compliant cGMP programs will be detailed.  Additionally, attendees will form a foundational understanding of the FDA's “Quality Systems Approach to Pharmaceutical cGMP Regulations."  Other topics such as the selection and qualification of vendors, along with risk management and validation concerns will also be discussed in detail.
 
 
Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
 
Deadline for Abstracts: n/a
 
Registration: http://www.cfpie.com/showitem.aspx?productid=095&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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