Historical
ANSI/AAMI/ISO 13408-7:2012
Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products
Specifies requirements and provides guidance on alternative approaches to process simulations for the qualification of the aseptic processing of medical devices and combination products that cannot be terminally sterilized and where the process simulation approach according to ISO 13408-1 cannot be applied. This part of ISO 13408 describes how risk assessment can be used during the development of an a septic process to design a process simulation study for medical devices and combination products in those cases where a straightforward substitution of media for product during aseptic processing is not feasible or would not simulate the actual aseptic process.
Content Provider
Association for the Advancement of Medical Instrumentation [aami]
