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EO Sterilization Control and Validation – Necessity and Requirements
- Date: March 17, 2010
- Source: Admin
Abstract:Sterilization validation is a topic of immense relevance as it pulls many audit observations from the FDA and international regulatory bodies. For medical device sterilization, comparing to other modes such as steam sterilization and etc, EO works in relatively low pressure temperature and therefore, has been regarded as one of the most excellent and useful method of medical device sterilization.
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