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STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013)
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Available format(s): Hardcopy, PDF
Superseded date: 07-03-2021
Language(s): English
Published date: 01-07-2006
Publisher: German Institute for Standardisation (Deutsches Institut für Normung)
This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
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