Good Laboratory Practice a Process to Assure Reliable Data in the Testing of Chemicals

Authors

  • Milan Škrlj

DOI:

https://doi.org/10.5644/Radovi.311

Abstract

Good laboratory practice is an expression of a need for harmonization of the work in laboratory Services to ensure adequate product quality. The system of laboratory work should be accompanied by an inspection and study audit. The document Principles of Good Laboratory Practice in Chemicals investigation, adopted by the OECD Council in 1981, represents a basis for international exchange of information of toxicological and other data. The GLP includes responsibilities in management, quality of work, facilities, documentation, study plan, objectives of the study, equipment, personnel etc. The inspection and study audit on GLP performance should be realized through relevant authority (government).

References

Good Laboratory Practice in the Testing of Chemicals, OECD, Paris, 1982.

Application of GMP Rtdes in the Control Laboratorv, Zbornik radova izloženih na Seminaru u Budimpešti od 10—12. juna 1981. godine.

Good Laboratorv Practice — a Process to Assure the Quality of Test Data in the Testing of Chemicals, ENV/CHEM/MC/82.5, OECD, Pariz, 1982.

Certification Scheme on the Quality of Pharmacentical Products Moving in International Commerce, PHARM/82.4, WH0, Ženeva.

Published

13.09.1991

Issue

Section

Works

How to Cite

Good Laboratory Practice a Process to Assure Reliable Data in the Testing of Chemicals. (1991). Acta Medica Academica, 25, 277-283. https://doi.org/10.5644/Radovi.311