This book explains the importance and practice of pediatric drug testing for pharmaceutical and toxicology professionals. It describes the practical and ethical issues regarding non-clinical testing to meet US FDA Guidelines, differences resulting from the new European EMEA legislation, and how to develop appropriate information for submission to both agencies. It also provides practical study designs and approaches that can be used to meet international requirements. Covering the full scope of non-clinical testing, regulations, models, practice, and relation to clinical trials, this text offers a comprehensive and up-to-date resource.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
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 Services, Horsham, PA.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : killarneybooks, Inagh, CLARE, Irlande
Hardcover. Etat : Near Fine. 1st Edition. Hardcover, xv + 339 pages, NOT ex-library. Printed in the USA. Interior is clean and bright throughout, with unmarked text, free of inscriptions and stamps, firmly bound. Minor handling marks on page edges externally. Boards show gentle shelfwear. Issued without a dust jacket. -- This work serves as a comprehensive and practical guide to the principles and practice of non-clinical (animal) safety testing for drugs intended for pediatric populations. It provides a detailed overview of the specific regulatory requirements from key agencies like the FDA and EMA. The book systematically covers the design and execution of juvenile animal studies, addressing the unique challenges of toxicology testing in developing organisms. It details age-appropriate study design, endpoint selection, and the interpretation of data in the context of developmental milestones. The volume is an essential reference for toxicologists, pharmacologists, and regulatory affairs professionals involved in the development of medicines for children. N° de réf. du vendeur 011890
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Vendeur : Basi6 International, Irving, TX, Etats-Unis
Etat : Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service. N° de réf. du vendeur ABEOCT25-92420
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Vendeur : Romtrade Corp., STERLING HEIGHTS, MI, Etats-Unis
Etat : 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. N° de réf. du vendeur ABBB-52077
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Vendeur : Books Puddle, New York, NY, Etats-Unis
Etat : New. pp. 356 Index. N° de réf. du vendeur 264660321
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Vendeur : GreatBookPrices, Columbia, MD, Etats-Unis
Etat : New. N° de réf. du vendeur 5767217-n
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Etat : New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed. N° de réf. du vendeur SNTA-52077
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Vendeur : Majestic Books, Hounslow, Royaume-Uni
Etat : New. pp. 356. N° de réf. du vendeur 3187646
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Vendeur : Brook Bookstore On Demand, Napoli, NA, Italie
Etat : new. N° de réf. du vendeur 48c648f5ded9cdb3719338503b115ad1
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Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
Etat : New. pp. 356 Acknowledgements. N° de réf. du vendeur 184660331
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Vendeur : PBShop.store UK, Fairford, GLOS, Royaume-Uni
HRD. Etat : New. New Book. Shipped from UK. Established seller since 2000. N° de réf. du vendeur FW-9780470448618
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