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ANSI/AAMI/ISO 13408-4:2005/(R)2014

Aseptic processing of health care products—Part 4: Clean-in-place technologies

Summary

This document specifies the general requirements for clean-in-place (CIP) processes applied to product contact surfaces of equipment used in the manufacture of sterile health care products by aseptic processing and offers guidance on qualification, validation, operation and control. This document applies to processes where cleaning agents are delivered to the internal surfaces of equipment designed to be compatible with CIP that may come in contact with the product. Annex 3

Technical characteristics

Publisher Association for the Advancement of Medical Instrumentation (AAMI)
Publication Date 01/01/2005
Confirmation Date 01/01/2014
Page Count 0
Themes Sterilization—Industrial
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