Current status and use of short/medium-term models for assessment of carcinogenicity of human pharmaceuticals: regulatory perspectives

Author:

van der Laan Jan Willem

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference11 articles.

1. Carcinogenicity testing and evaluation of regulatory requirements for pharmaceuticals;Contrera;Regul. Pharmacol. Toxicol.,1997

2. Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA;De Vries;Nature,1995

3. Neonatal mouse assay for tumorigenicity: alternative to the chronic rodent bioassay;Flammang;Regul. Pharmacol. Toxicol.,1997

4. Evaluation of the newborn mouse model for chemical tumorigenesis;Fujii;Carcinogenesis,1991

5. ICH, 1997. International Conference on Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use. Harmonised guideline. Testing for Carcinogenicity of Pharmaceuticals, CPMP/ICH/299/95.

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