Pharmaceutical Toxicology in Practice: A Guide to Non-Clinical Development PDF (Adobe DRM) download by Alberto Lodola

Pharmaceutical Toxicology in Practice: A Guide to Non-Clinical Development

Wiley
Publication date: March 2011
ISBN: 9780470909904
Digital Book format: PDF (Adobe DRM)

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This book describes, with references to key source materials, the background to, and conduct of, the principal nonclinical studies that are central to drug development. The chapters provide an understanding of the key components of the preclinical phase of drug development with a hands-on description, with core chapters addressing study conduct, types, and reporting. As such, it is a practical guide through toxicology testing and an up-to-date reference on current issues, new developments, and future directions in toxicology. Opening with a practical description of toxicology and its role in the development of pharmaceuticals, the book proceeds to detail international regulations (including the impact of the new REACH standards for chemical safety), interdisciplinary interactions among scientists in drug development, steps in toxicity testing, and risk management. Further, the book covers the methods of genetic toxicology (assays, genomics, in vivo screening) as a complement to “traditional” toxicology in the risk assessment and risk management of pharmaceuticals.
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Pharmaceutical Toxicology in Practice: A Guide to Non-Clinical Development PDF (Adobe DRM) download by Alberto Lodola
Wiley, March 2011
ISBN: 9780470909904
EAN:  9780470909904
PDF (Adobe DRM)
List Price: $94.99 eBook price: $91.99
Pharmaceutical Toxicology in Practice: A Guide to Non-Clinical Development ePub (Adobe DRM) download by Alberto Lodola
Wiley, March 2011
ISBN: 9780470922729
EAN:  9780470922729
ePub (Adobe DRM)
eBook price: $91.99