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Pharmaceutical cGMPs and FDA Inspections

 
  July 09, 2007  
     
 
The Center for Professional Advancement, Boca Raton, FL
November 12-14, 2007


Who Should Attend:
This is an ideal course to acquire current applications of cGMPs. It offers latitude for discussion of fundamental as well as evolving regulatory initiatives and other complex issues. The course is distinguished for benefit to domestic as well as non-US enterprises, including the following:

Positions
Analysts, Directors, Engineers, Executives, Investigators, Internal Auditors, Managers, Operators, QA/QC, Research, Supervisors, and Trainers

Industries
Academia, Biogeneric, Biological, Biopharmaceutical, Combination Product Manufacturers, Consultants, Contract Manufacturing, Dietary Supplements, Health Care, Legal Pharmaceutical. Regulatory, and Many Others…


Description:
This course takes you through Current Good Manufacturing Practice (cGMP) in the pharmaceutical and allied industries. Topics covered include legal requirement for cGMP in the Federal Food, Drug, and Cosmetic Act and related regulations. It addresses practical aspects of personnel, facilities, equipment, components, manufacturing, laboratory, packaging, labeling and QA/QC and provides an excellent forum for training personnel in cGMPs. The faculty consists of individuals with long and distinguished experience in the field. Throughout this course, the relevance of FDA inspections commonly surfaces. There is special emphasis on discussing procedures and practices of the regulatory agency to help firms comprehend management of FDA relationships.

 
 
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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