Good Laboratory Practice and Study Management for the Validation of In Vitro Toxicity Studies

Alternatives to Laboratory Animals

Volumn 25, Issue 5, 1997, Pages 527-537

  Cooper Hannan, Robin ^a  

^a Qualitas   (United Kingdom)

Author keywords

GLP; Good Laboratory Practice; In vitro toxicity studies; Interlaboratory; Principal Investigator; Study Director; Study management; Validation

Indexed keywords

EID: 2542553441     PISSN: 02611929     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Balls, M., Blaauboer, B.J, Fentem, J.H., Bruner, L., Combes, R.D., Ekwall, B., Fielder, R.J, Guillouzo, A., Lewis, R.W., Lovell, D.P., Reinhardt, C-A., Repetto, G., Sladowski, D., Spielmann, H. & Zucco, F (1995). Practical aspects of the validation of toxicity test procedures. The report and recommendations of ECVAM workshop 5. ATLA 23, 129-147.
2. Anon. (1996). Final Report of the OECD Workshop on Harmonization of Validation and Acceptance Criteria for Alternative Toxicological Test Methods, 60 pp. Paris: OECD
3. Anon. (1992). Environment Monograph No. 45: The OECD Principles of Good Laboratory Practice 1, 29 pp. Paris. OECD.
4. Anon. (1995), Environment Monograph No. 116: OECD: The Application of the Principles of GLP to Computerised Systems, 15 pp. Paris. OECD.