9780470448618 - pediatric non-clinical drug testing: principles, requirements, and practice (7 Ergebnisse)
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Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
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Zustand: New. pp. 356.
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HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
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EUR 127,60
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Zustand: New. ALAN M. HOBERMAN, PhD, DABT, Fellow ATS, is Executive Director of Site Operations and Toxicology at Charles River Preclinical Services, Horsham, PA.ELISE M. LEWIS, PhD, is Director of Reproductive and Neurobehavioral Toxicology at Charles River Preclinical .
- Hardcover
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Zustand: New. This book explains the importance and practice of pediatric drug testing for pharmaceutical and toxicology professionals. Editor(s): Hoberman, Alan M.; Lewis, Elise M. Num Pages: 356 pages, Illustrations. BIC Classification: MJ; MM; PN. Category: (P) Professional & Vocational. Dimension: 162 x 241 x 28. Weight in G…rams: 708. . 2012. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.
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Anbieter: AHA-BUCH GmbH, Einbeck, DeutschlandAHA-BUCH GmbH
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EUR 174,00
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Buch. Zustand: Neu. Neuware - Enables readers to successfully perform non-clinical drug testing, meeting international requirementsAlthough the non-clinical and clinical testing needs of drugs for pediatric populations have been discussed and debated for more than forty years, many ethical, political, and practical issues remain… unresolved, making pediatric drug testing and labeling a challenge for pharmaceutical and toxicology professionals. Written and edited by a team of leading international experts, this book explains both the importance and the practice of non-clinical pediatric drug testing. Moreover, it guides readers through the complex set of international rules and regulations governing the practice today.Following the authors' clear advice, readers will be able to meet FDA guidelines for non-clinical pediatric drug testing, from initial study design to submission of results for approval. Moreover, the authors describe key differences between the FDA guidelines and European Medicines Agency (EMA) legislation, enabling readers to devise and conduct studies, analyze the results, and then compile appropriate information for submission to both agencies.Pediatric Non-Clinical Drug Testing offers clear guidance for managing the key challenges of non-clinical testing models, helping readers overcome the difficulties associated with:Lack of fully comparable modelsInadequate historical experienceSpecific needs and effects associated with testing animalsPractical problems using the clinical route of exposure in animal modelsThe book's appendix features a sample juvenile toxicity testing protocol that readers can use as a template for their own experimental designs.In addition to toxicologists and pharmacokineticists, this book is recommended for drug regulators who need to develop and enforce drug testing standards to protect children. It is also recommended as a textbook for toxicology and pediatric medicine courses.
