GB/T 42502-2023
ActiveSpecification for auditing quality management of pharmaceutical logistics
医药物流质量管理审核规范
Application Summary AI generated
This standard specifies the auditing requirements for quality management systems in pharmaceutical logistics, including storage, transportation, and distribution processes. It is applied by logistics service providers, pharmaceutical companies, and regulatory auditors to ensure compliance with Good Distribution Practice (GDP) and product integrity throughout the cold chain. The standard is particularly relevant in China for verifying temperature control, documentation, and handling procedures in the pharmaceutical supply chain.
Related Standards
GB/T 2828.1-2012
Sampling procedures for inspection by attributes — Part 1: Sampling schemes indexed by acceptance quality limit (AQL) for lot-by-lot inspection
GB/T 19011-2013
Guidelines for auditing management systems
GB/T 19000-2008/ISO 9000:2005
Quality management systems - Fundamentals and vocabulary
GB/T 19004-2011
Managing for the sustained success of an organization — Quality management approach
GB/T 2828.1-2003
Sampling procedures for inspection by attributes--Part 1: Sampling schemes indexed by acceptance quality limit(AQL) for lot-by-lot inspection
GB/T 19022-2003
Measurement management systems--Requirements for measurement processes and measuring equipment
GB/T 6379.1-2004
Accuracy(trueness and precision)of measurement methods and results--Part 1:General principles and definitions
GB/T 6379.2-2004
Accuracy(trueness and precision)of measurement methods and results--Part 2:Basic method for the determination of repeatability and reproducibility of a standard measurement method
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.