home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Courses and Workshops  
 

cGMP for Pharmaceutical Production Supervisors

 
  November 20, 2007  
     
 
The Center for Professional Advancement, New Brunswick, NJ
April 1-3, 2008


Who Should Attend
This practical course is intended for professionals in the pharmaceutical, cosmetic and related industries, including:
  • First-line production
  • Foremen
  • Quality control supervisors
  • Group leaders of incoming inspection
It is most beneficial to manufacturing personnel involved in:
  • Packaging
  • Materials handling
  • In-process inspecting
  • Final inspecting
  • Maintenance and warehousing
  • Processing
Higher level technical and managerial personnel will find the course a worthwhile refresher of the basics and interpretive aspects of the regulations.

Description
This course will provide an orientation and understanding of the Current Good Manufacturing Practice segment of the U.S. Food, Drug, and Cosmetic Act. The course will cover supervisory techniques and practices for complying with the U.S. FDA regulations in packaging, assembly, production and manufacturing. It will provide a practical application of the cGMP on the operating level. Actual experiences and case studies will be included. Ample time will be given to the specific problems of participants. This course will prepare firstline supervisors and other plant manufacturing personnel to successfully discharge their responsibility for implementing a company's cGMP program.

 
 
Organized by: The Center for Professional Advancement
Invited Speakers: Dr. Mary Foster ,VP Regulatory Compliance, Catalent Pharma Solutions (formerly Cardinal Health, PTS)

Dr. Mary Foster is VP Regulatory Compliance for Catalent Pharma Solutions (formerly Cardinal Health, PTS). In this role Dr. Foster is responsible for helping to develop and implement the policies and programs for PTS business units to ensure regulatory compliance. The programs are relative to various regulatory agencies including, USA, EU, Japan, and Australia and cover federal regulations (cGMP, cGCP and cGLP) and guidelines. She has prepared procedural manuals and has adapted this material to training programs for operation personnel. Dr. Foster received her Doctor of Pharmacy and Bachelor of Science degrees from the University of Kentucky.

 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: info@cfpa.com
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.