Good Laboratory Practice (GLP) 

This area of the website is devoted to those who are interested in Good Laboratory Practice (GLP) issues. We aim to provide the latest information on international regulatory guidelines and laws, intelligence across the discipline and information on the sectors developments.

Please click on the RQA GLP Committee to find out information on the Committee and its activities.

---

Have a Say in updates to the OECD GLP Consensus & Advisory Documents

Submit your input by 13 March 2026.

The OECD GLP IDG (Industry Discussion Group) has an opportunity to provide the OECD GLP Working Party (WP) with recommendations regarding the possible revision of GLP Consensus and Advisory Documents. We sincerely hope that you take the opportunity to contribute and tell us through the questionnaire which documents need to be revised/updated, with why, and what should be modified. To facilitate the collection of comments we propose the use the attached form. The survey has 2 objectives: 1. Revision list- Need for revisions of the GLP Consensus and Advisory Documents. 2. Additional Questions – Other topics that require guidance, issues with GLP certificates or routine MA inspection programmes, real life situations relating to collecting test item characterization data from Sponsors/CMOs. The due date is Friday 13 March 2026. All comments will be considered to prepare the document that will be submitted to the OECD GLP WP.

Link: OECD GLP Industry Discussion Group (IDG) Survey (United Kingdom) – Fill in form