GB/T 22275.7-2008
ActiveRequirements of conduct for good laboratory practice - Part 7: The application of the GLP principles to the organisation and management of multi-site studies
良好实验室规范实施要求 第7部分：良好实验室规范原则在多场所研究的组织和管理中的应用
Application Summary AI generated
This standard specifies the requirements for applying Good Laboratory Practice (GLP) principles to the organization and management of studies conducted across multiple test sites. It is used by laboratories, contract research organizations, and regulatory bodies in China to ensure data integrity and quality control when a single study involves different locations, such as in chemical safety testing or pharmaceutical development. The standard applies to the planning, coordination, and documentation of multi-site studies to maintain compliance with GLP regulations.
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 19004-2011
Managing for the sustained success of an organization — Quality management approach
GB/T 19000-2008/ISO 9000:2005
Quality management systems - Fundamentals and vocabulary
GB/T 19011-2013
Guidelines for auditing management systems
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.