ISO-13408-4 Aseptic processing of health care products - Part 4: Clean-in-place technologies

ISO-13408-4 - 1ST EDITION - CURRENT


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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.

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Document Number

ISO 13408-4:2005

Revision Level

1ST EDITION

Status

Current

Publication Date

Nov. 1, 2005

Committee Number

ISO/TC 198