This part of YY/T 0567 specifies the basic requirements for the cleaning-in-place (CIP) process of product contact surfaces of equipment used to produce medical care products according to aseptic processes, and provides guidance for identification, validation, operation and control. This section applies to processes using cleaning agents on internal surfaces of equipment designed to be CIP-compatible and that may come into contact with product. This section does not apply to the process of disassembling equipment and cleaning it in a cleaning machine. This section does not replace or supersede national regulatory requirements, such as good manufacturing practices (GMP) and/or pharmacy requirements belonging to a specific country or region.
YY/T 0567.4-2011 Referenced Document
GB/T 19003 Software engineering.Guidelines for the application of GB/T 19001-2000 to computer software
YY/T 0567.1 Aseptic processing of health care products.Part 1:General requirements*, 2013-10-21 Update
YY/T 0567.4-2011 history
2011YY/T 0567.4-2011 Aseptic processing of health care products.Part 4:Clean-in-place technologies