Standard Swedish standard · SS-ISO 13408-7:2012

Aseptic processing of health care products - Part 7: Alternative processes for atypical medical devices and combination products (ISO 13408-7:2012, IDT)

Status: Valid

This part of ISO 13408 specifes requirements and provides guidance on alternative approaches to process simulations for the qualifcation 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 aseptic 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.


Sterilization and disinfection in general (11.080.01) Disinfectants and antiseptics (11.080.20) Other (11.080.99)

Product information

Language: English

Written by: SIS - Hälso- och sjukvård

International title:

Article no: STD-88280

Edition: 1

Approved: 12/6/2012

No of pages: 32