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Pharmaceutical Water Systems: Contemporary Technology & Compliance

 
  February 16, 2010  
     
 
The Center for Professional Innovation & Education, Costa Mesa, CA
May 17 & 18, 2010


Who Should Attend

Successful specification, design, installation, validation, management and control of a pharmaceutical water system depends on a coordinated, multi-disciplinary approach.  The course will be valuable for those in pharmaceutical, biotechnology and medical device manufacturing who are responsible for or involved in:

  • Specification and engineering design
  • Technical and validation support
  • Regulatory compliance activities and auditing
  • Risk assessment, troubleshooting and system improvement
  • Water system operation, management and maintenance
  • Quality assurance and validation management
  • Quality control, sampling, microbiological and chemical analysis



Learning Objectives


Upon completion of this course you will:

  • Understand the water types, qualities, uses and applications in pharmaceuticals, biotechnology and medical device manufacture
  • Be familiar with the applications and limitations of the range of treatment technologies and able to choose the most effective combination of techniques for your needs
  • Appreciate the importance of a “common-sense” approach to the implementation of cost-effective design solutions
  • Be aware of the GMP requirements and regulatory expectations relating to water systems and their validation requirements
  • Have gained a practical understanding of systems via examples and discussions
  • Have developed better knowledge and understanding between the different disciplines involved in the operation and management of water systems

The course will also provide interactive workshops and a discussion forum to enable delegates to exchange ideas and experience.



Course Description

This course provides an interactive mix of lectures, workshops and discussions intended to highlight basic principles and technologies and how these are applied in practice to pharmaceutical water systems. The benefits from applying the principles discussed during the course will include:

  • Minimize time spent in troubleshooting deviations and failures
  • Set appropriate alert and action limits to avoid costly batch contamination
  • Avoid regulatory agency’s observations and compliance issues and reduce inspection frequencies by building a history of compliance

The course is intended to raise practical understanding and awareness for water system owners and managers, QA managers, regulatory compliance staff, microbiologists, engineers, validation specialists and operators.

 
 
Organized by: Center for Professional Innovation & Education
Invited Speakers: info@cfpie.com
 
Deadline for Abstracts: n/a
 
Registration: http://www.cfpie.com/showitem.aspx?productid=093&source=hummolgen
E-mail: info@cfpie.com
 
   
 
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