Requirements

OECD Series on Principles of Good Laboratory Practice (GLP) and Compliance Monitoring - OECD

• No.1, OECD Principles on Good Laboratory Practice
• No.2, Revised Guides for Compliance Monitoring Procedures for Good Laboratory Practice
• No.3, Revised Guidance for the Conduct of Laboratory Inspections and Study Audits
• No.4, Quality Assurance and GLP
• No.5, Compliance of Laboratory Suppliers with GLP Principles
• No.6, The Application of the GLP Principles to Field Studies
• No.7, The Application of the GLP Principles to short-term Studies
• No.8, The Role and Responsibilities of the Study Director in GLP Studies
• No.9, Guidance for the Preparation of GLP Inspection Reports
• No.11, The Role and Responsibility of the Sponsor in the Application of the Principles of GLP
• No.12, Requesting and Carrying out Inspections and Study Audits in another country
• No.13, The Application of the OECD Principles of GLP to the Organisation and Management of Multi-site Studies
• No.14, The Application of the Principles of GLP to in vitro Studies
• No.15, Establishment and Control of Archives that Operate in Compliance with the Principles of GLP
• No.16, Guidance on the GLP Requirements for Peer Review of Histopathology
• No.17, Application of GLP Principles to Computerised Systems
• No.19, Management, Characterisation and Use of Test Items
• No.22, GLP Data Integrity
• No. 23, Advisory Document of the Working Party on Good Laboratory Practice on Quality Assurance and GLP

OECD documents