Mark | Date Date | Title Title | |||
---|---|---|---|---|---|
No. 10 | 05 Oct 1995 |
The Application of the Principles of GLP to Computerised Systems
This document specifies the application of the Principles of Good Lab Practice regarding the use of computerised systems. |
|||
No. 14 | 01 Dec 2004 |
The Application of the Principles of GLP to in vitro Studies
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. |
|||
No. 8 | 15 Sept 1999 |
The Role and Responsibilities of the Study Director in GLP Studies
This document defines the roles and responsibilities of the Study Director in Good Laboratory Practice studies. |
|||
No. 11 | 22 Jan 1998 |
The Role and Responsibility of the Sponsor in the Application of the Principles of GLP
This document defines the role and responsibility of the sponsor in the application of the Principles of Good Laboratory Practice. |
|||
03 Sept 2014 |
‘Outsourcing' of Inspection Functions by Glp Compliance Monitoring Authorities
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. |
OECD Series on Principles of Good Laboratory Practice and Compliance Monitoring
- Discontinued
This is the complete set of the series on OECD Principles of Good Laboratory Practice (GLP) which set the quality standards for the organisation and management of test facilities and for performing and reporting studies related to the safety of chemical substances and preparations. The GLP Principles cover all aspects of a laboratory’s daily activity, such as the layout of testing and storage areas to prevent contamination, cleaning and calibration of equipment, handling of test animals, and recording and archiving of test results. The GLP Principles thereby help ensure that studies submitted to regulatory authorities, to notify or register chemicals, are of sufficient quality and rigour and are verifiable.
Also available in: French
- ISSN: 2077785X (online)
- https://doi.org/10.1787/2077785x