Back

ISO 13408-4:2005

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

General information
Valid from 28.10.2005
Directives or regulations
None
Standard history
Status
Date
Type
Name
28.10.2005
Main
ISO 13408-4:2005 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. ISO 13408-4:2005 is applicable to processes where cleaning agents are delivered to the internal surfaces of equipment designed to be compatible with CIP, which may come in contact with the product. ISO 13408-4:2005 is not applicable to processes where equipment is dismantled and cleaned in a washer. ISO 13408-4:2005 does not supersede or replace national regulatory requirements, such as Good Manufacturing Practices (GMPs) and/or compendial requirements that pertain to particular national or regional jurisdictions.
*
*
*
PDF
101.81 € incl tax
Paper
101.81 € incl tax
Standard monitoring