How to reduce EO residuals in medical devices 2011

25 Feb 2011

Webinar

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

How to reduce EO residuals in medical devices 2011 - 25 Feb 2011, Webinar (9744)

How to reduce EO residuals in medical devices 2026

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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