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Microbiological Control and Validation

  June 06, 2011  
CfPA - The Center for Professional Advancement, Amsterdam, The Netherlands
17-19 October 2011

Who Should Attend
The course is designed for professionals in the medical device, biotechnology and pharmaceutical industries including:

  • Those needing a basic knowledge of microbiology as it
    affects their function
  • Microbiology personnel who wish to get updated on new,
    more reliable rapid testing, monitoring and identification
  • Audit personnel needing more background in the
    microbiological aspects to be considered when auditing
  • Personnel with little background in microbiology, such as
    manufacturing, validation, and facilities staff that need to
    gain a better understanding of how to better deal with
    microbiological issues

This course will present information on microbiological control in manufacturing, laboratory auditing and sterilization. The course will also cover ISO, EP, BP, USP, AAMI and U.S. FDA documents and guidelines. Validation of sterilization processing will be discussed and case studies will be presented. Environmental monitoring programs will be discussed in depth. Design and testing of product packages for sterility assurance will be covered via case studies. All aspects of microbiological control will be covered. Microbiological testing schemes will be presented and the key aspects of GLP/cGMP will be reviewed.

You are invited to bring transparencies of monitoring programs, procedures, flowcharts, etc., for discussions during the case studies on the third day.

Organized by: CfPA - The Center for Professional Advancement
Invited Speakers: William Marshall; President, William G. Marshall and Associates

William G. Marshall, President of William G. Marshall and Associates, has over twenty years experience in the Pharmaceutical and Medical Device Manufacturing Environment. Mr. Marshall has held Director level and Chief Operating Officer positions with large multinational corporations as well as start-up ventures. He has been the Director of a major reference laboratory and has been active in clean room design and validation. In the last five years he has acted as a third party in several consent decrees.

Mr. Marshall is currently a consultant to the worldwide drug and device industry as well as to the FDA. He lectures worldwide in GMP related issues including clean room technology and sterilization.
Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: sberg@cfpa.com
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