This document provides guidance to pathologists, test facility management, study directors and quality assurance personnel on how the peer review of histopathology should be planned, managed, documented and reported in order to meet GLP expectations...

This document provides guidance concerning the establishment and control of archives compliant with the principles of Good Laboratory Practice, and is intended for use by test facilities, contract archives and quality assurance units and comliance...

This document facilitates the proper application and interpretation of the GLP Principles for the organisation and management of in vitro studies, and provides guidance for the appropriate application of the GLP Principles to in vitro studies.

This document provides guidance on the issues that are involved in the planning, performance, monitoring, recording, reporting and archiving of multi-site non-clinical health and environmental safety studies.

This document sets out recommended procedures to use when requesting and carrying out inspections and study audits in another country under the Principles of Good Lab Practice and Compliance Monitoring.

This document defines the role and responsibility of the sponsor in the application of the Principles of Good Laboratory Practice.

This document specifies the application of the Principles of Good Lab Practice regarding the use of computerised systems.

This document suggests elements and/or concepts that can contribute to a useful report of a Good Laboratory Practice inspection and study audit. It may be used by Member countries as a component of their compliance monitoring programme.

This document defines the roles and responsibilities of the Study Director in Good Laboratory Practice studies.

This document cites the appropriate OECD Principles of GLP and gives guidance on their interpretation in relation to short-term studies in a series of notes.

This document specifies the application of the Good Laboratory Practice principles to field studies, interpreting such concepts as study, test site, study director, management responsibilities, quality assurance, etc. for application in this specific...

This document offers advice to both test facility management and suppliers as to how they might meet GLP requirements through national accreditation schemes and/or working to formal national or international standards, or by adopting other measures.

This document defines quality assurance programmes required to meet Good Laboratory Practice princples.

This document provides guidance for the conduct of laboratory inspections and study audit under the Principles of Good Laboratory Practice.

This document provides detailed practical guidance to OECD Member countries on the structure, mechanisms and procedures they should adopt when establishing national Good Laboratory Practice compliance monitoring programmes.

This document provides the full text of the OECD Principles of Good Laboratory Practice as revised in 1997. These principles cover the organisational process and the conditions under which laboratory studies are planned, performed, monitored,...

This document reiterates the decisions and the recommendations related to the role and responsibilities of governments, national GLP compliance monitoring authorities and inspectors with regard to outsourcing.