Aseptic processing of health care products - Clean-in-place technologies1 Scope This part of ISO 13408 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 part of ISO 13408 is applicable to processes where cleaning agents are delivered to the internal surfaces of equipment designed to be compatible with

extensions

values and descriptions within new or revised TC 192 standards and to ensure such definitions are clearer

variable focal length lenses

IEC 61508-3:1998

BS EN 3745-305 specifies a method of measuring the immunity of optical fibre or cable to the coupling of power coming from an external light source

insulating and protective material

It is unsuitable for rough-surfaced materials

Power Distribution Companies

Four classes of gear are specified

including wall-fixed mirrors

Note: The method does not apply completely to alloys having silicon contents greater than 1 % (m/m)

Healthcare operators/hospitals/clinics