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Pharmaceutical toxicology or safety assessment is, through and through, a translational discipline. All aspects of preclinical safety activities aim at identifying potential hazards, predicting and quantifying risks for healthy trial subjects or patients, and, if necessary, assessing suitable means for eliminating or reducing unacceptable risks. However, there are many uncertainties in this approach. For practical reasons, only a limited number of aspects can be addressed in preclinical animal and in vitro studies. Furthermore, considerable species differences leading to changes in biological activity or pharmacokinetic properties as well as individual variations in susceptibility to certain effects and compounds add to uncertainties in the risk-assessment process. Thus, any toxicological risk-assessment process for pharmaceutical or other compounds is always incomplete and associated with uncertainties. Such uncertainties are compensated for by empirically derived safety factors.
Case Report: Journal of Drug Metabolism & Toxicology
Commentary: Journal of Drug Metabolism & Toxicology
Review Article: Journal of Drug Metabolism & Toxicology
Research Article: Journal of Drug Metabolism & Toxicology
Editorial: Journal of Drug Metabolism & Toxicology
Research Article: Journal of Drug Metabolism & Toxicology
Editorial: Journal of Drug Metabolism & Toxicology
Research Article: Journal of Drug Metabolism & Toxicology
Research Article: Journal of Drug Metabolism & Toxicology
Scientific Tracks Abstracts: Medicinal & Aromatic Plants
Posters-Accepted Abstracts: Journal of Pharmaceutical Care & Health Systems
Posters & Accepted Abstracts: Biochemistry & Pharmacology: Open Access