Genetic toxicology testing requirements: Official and unofficial views from europe

Author:

Kirkland D. J.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Genetics (clinical),Epidemiology

Reference12 articles.

1. The prospects for a simplified and internationally harmonized approach to the detection of possible human carcinogens and mutagens

2. CPMP (1989): Commission of the European Communities; The rules governing medicinal products in the European Community, Volume III. Guidelines on the quality, safety and efficacy of medicinal products for human use, January 1989, p 103.

3. CPMP (1990): CPMP Working Party on Safety of Medicinal Products. Note for Guidance. Recommendations for the development of non-clinical testing strategies. III/58/89-EN. Draft Number 7, 5 July 1990.

4. Department of;DH,1989

5. EEC (1984): Annex V to EEC Directive 79/831/EEC, Part B: Methods for the Determination of Toxicity. Official Journal of the European Communities, L251, Vol. 27, 19 September 1984. K H Narjes, EEC, Brussels.

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