This guidance provides clarity for test facilities on the expectations of national Good Laboratory Practice (GLP) compliance monitoring authorities on how test items are transported, received, identified, labelled, sampled, handled, stored, characterised, archived and disposed. The document consolidates existing OECD guidance on test items that are used in studies conducted in compliance with the Principles of GLP. It also aims to promote a consistent approach that is appropriate to the objective of the study and the nature of the test item.
Management, Characterisation and Use of Test Items used in GLP studies
Report
Share
Facebook
Twitter
LinkedIn
Abstract
In the same series
-
2 December 202413 Pages
-
18 July 202215 Pages
-
7 May 202014 Pages
-
Report23 July 201919 Pages
-
Report9 February 201612 Pages
Related publications
-
2 July 2026115 Pages
-
Report2 July 202632 Pages
-
2 July 202615 Pages
-
Report
Assay for the Detection of Glucocorticoid Receptor Agonist and Antagonist Activity of Chemicals
2 July 202634 Pages -
Report
Assays addressing the Adverse Outcome Pathway key event on covalent binding to proteins
2 July 202663 Pages -
Report
Assays addressing the Adverse Outcome Pathway Key Event on Keratinocyte activation
2 July 202698 Pages