ETO Sterilizer Validation

ETO Validation is the documented procedure for obtaining, recording and interpreting the results required to establish that the sterilization process will consistently yield a product complying with predetermined specifications (ISO 11135:2014). Validation of the ETO sterilization process yields a documented procedure of consistently confirming the inactivation of all living microorganisms, confirmation that the product or device is sterile, and confirmation that the process is repeatable. The process validation is a key factor in any regulator with standard compliance technique. IETQAN can concurrently validate more than one sterilizer at a time. Reports are traceable and verifiable through IETQAN web site. This way you will be able to share the report with regulatory agencies and clients with high credibility level.

A European Authorised Representative (E.A.R.) serves as a legal entity designated by non European Union (EU) manufacturers, to represent them in the EU and ensure their compliance with the European Directives/Regualtions

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