GB/T 36030-2018
ActiveGeneral technical requirements of CIP and SIP for pharmaceutical machinery
制药机械(设备）在位清洗、灭菌通用技术要求
Application Summary AI generated
This standard specifies the general technical requirements for Clean-in-Place (CIP) and Sterilization-in-Place (SIP) systems used in pharmaceutical machinery. It is applied in the design, manufacturing, and validation of equipment for the pharmaceutical industry, ensuring that internal surfaces of tanks, pipes, and processing equipment can be effectively cleaned and sterilized without disassembly. The standard is critical for maintaining hygiene and preventing cross-contamination in drug production facilities.
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Transparency note: The application summary and key sentences on this page were automatically generated by AI from the standard's original text. This content has not been human-verified and should not be used for compliance or regulatory purposes. Always refer to the official standard document from the issuing authority.