Reducing Ethylene Oxide (EO) Sterilization Costs While Maintaining Regulatory Compliance

In this Ethylene Oxide (EO) Sterilization training, you will learn how to evaluate your sterilization process for cost reduction/process efficiency, and also learn how to implement such changes without jeopardizing product safety and regulatory compliance.

Why Should You Attend:

Many medical device manufacturers are not taking advantage of latest sterilization technologies and knowledge to effectively reduce the sterilization process cost. This is due mainly to: lack of knowledge of latest technologies, fear of getting out of regulatory compliance or belief that changes to the sterilization process are too complex or risky.

Areas Covered in the Seminar:

• Introduction.
• Factors Influencing Lethality and Aeration.
• Finding Opportunities for Cycle Optimization.
  • Negotiate cost reduction
  • Initial Validation Evaluation
  • Microbiological Method
  • Cycle Parameters Evaluation
  • EO residues dissipation curves
  • Product Evaluation
• Cycle/Process Re-engineering
  • BI Incubation reduction
  • Parametric Release
  • PCD/Packaging/Pallet modification
  • Lethality curve development
  • Aeration modification
• References.

Who Will Benefit:

This seminar is designed for professionals with responsibility for validating or making decisions related to the EO sterilization process.

• Sterilization/Quality Managers
• Directors and VP of manufacturing/ quality
• Quality or laboratory personnel
• Product Managers
• Regulatory Affairs
• Quality or laboratory personnel

Event Details:

Date:              August 31, 2012

Time:              10:00 AM - 11:00 AM PDT

Cost:              $249 per attendee per computer terminal

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