The purpose of this document is to facilitate the proper application and interpretation of the GLP Principles for the organisation and management of in vitro studies, and to provide guidance for the appropriate application of the GLP Principles to in vitro studies, both for test facilities (management, QA, study director and personnel), and for national GLP compliance monitoring authorities. This Advisory Document intends to provide such additional interpretation of the Principles and guidance for their application to in vitro studies carried out for regulatory purposes. It is organised in such a way as to provide easy reference to the GLP Principles by following the sequence of the different parts of these GLP Principles.
The Application of the Principles of GLP to in vitro 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
-
19 April 201820 Pages
Related publications
-
15 December 2025169 Pages
-
Report3 December 202594 Pages
-
30 June 2025193 Pages
-
Working paper30 June 2025250 Pages
-
30 June 2025329 Pages
-
Working paper30 June 2025270 Pages