How to reduce EO residuals in medical devices 2011

  • 25 Feb 2011
  • Webinar

Description

This Ethylene Oxide Sterilization Residuals regulation based webinar will provide a practical approach to fulfill requirements of the new ISO EO residual limits revised regulation.

Areas Covered in the Seminar:

  • Introduction.
    • Benefits/challenges
    • EO residual limits comparison

  • Factors influencing EO residuals
  • Product/Process Evaluation
    • Initial validation evaluation

    • Product /packaging/pallet configuration Evaluation

  • Process Re-engineering.
    • PCD/packaging/pallet modification
    • Lethality curve development
    • Aeration/Degassing Modification
    • Application of assumed transfer reduction factors

  • 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 or VP
  • Quality or laboratory personnel
  • Chemists
  • Chemistry laboratory Managers
  • Validation specialists

Past Events

Important

Please, check "How to reduce EO residuals in medical devices" official website for possible changes, before making any traveling arrangements

Event Categories

Education: Training
Health & Medicine: Medical laboratories
Industry: Chemicals
Science: Laboratories

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