| Literature DB >> 10088208 |
L G Friedlander1, S D Brynes, A H Fernández.
Abstract
The pre-approval risk assessment process for new animal drugs is described in this article. The toxicological and residue chemistry data needed by the FDA for the human food safety evaluation of a new animal drug is also discussed.Entities:
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Year: 1999 PMID： 10088208 DOI： 10.1016/s0749-0720(15)30203-6
Source DB: PubMed Journal: Vet Clin North Am Food Anim Pract ISSN： 0749-0720 Impact factor: 3.357