EN ISO 13408-5:2011

Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006) EN ISO 13408-5:2011

Publication date:   Aug 17, 2011

General information

60.60 Standard published   Jun 29, 2011

CEN

CEN/TC 204 Sterilization of medical devices

European Norm

11.080.01   Sterilization and disinfection in general

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Scope

ISO 13408-5:2006 specifies the general requirements for sterilization in place (SIP) applied to product contact surfaces of the equipment used in the manufacture of sterile health care products by aseptic processing and offers guidance on qualification, validation, operation and control.
ISO 13408-5:2006 applies to processes where sterilizing agents are delivered to the internal surfaces of equipment that can come in contact with the product.

Related legislation

Legislation related to this standard

98/79/EC

In vitro diagnostic medical devices

Harmonized/Supporting
93/42/EEC

Medical devices

Harmonized/Supporting
90/385/EEC

Active implantable medical devices

Harmonized/Supporting

Life cycle

PREVIOUSLY

WITHDRAWN
EN 13824:2004

NOW

PUBLISHED
EN ISO 13408-5:2011
60.60 Standard published
Jun 29, 2011

Relations

Adopted from ISO 13408-5:2006 IDENTICAL