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Provides guidance on the requirements of ISO 11135 that apply when parametric release is used to release the product after exposure to the sterilization process. Provides a path for transition of existing cycles, as well as a path for the development and implementation of a parametric release specification for a new cycle. Highlights the importance and interrelationship of other process factors, i.e. load configuration and equipment performance, which influence reproducibility of an ethylene oxide (EO) sterilization process.