Lexikon

Good Laboratory Practice (GLP) is a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported. (Source: REACH Glossary)
OECD Guidelines on Good Laboratory Practice part 1, available at: http://www.oecd.org/findDocument/0,2350,en_26...

GLP = Good Laboratory Practices
According to 2004/10/EC, Good Laboratory Practice (GLP) is defined as a quality system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported. The main objective of GLP is to ensure test data produced by different laboratories can be mutually recognized so as to avoid repeat testing. GLP provides an assurance to regulatory authorities that the data submitted are a true reflection of the results obtained during the study and can therefore be relied upon when making risk/safety assessments.

Member States of the European Union have to take measures to comply with the principle of GLP when evaluating chemicals safety according to 67/548/EEC. SGS has a worldwide network of laboratories that are GLP compliant contractual laboratories for physico-chemical, toxicological and ecotoxicological tests.

Source: REACH, Glossary