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Da: Basi6 International, Irving, TX, U.S.A.
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Da: SMASS Sellers, IRVING, TX, U.S.A.
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Da: SMASS Sellers, IRVING, TX, U.S.A.
Condizione: New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
Condizione: New. pp. vi + 258 Index.
EUR 86,98
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Aggiungi al carrelloCondizione: New. pp. vi + 258 Illus.
Da: Romtrade Corp., STERLING HEIGHTS, MI, U.S.A.
Condizione: 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.
Condizione: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
Da: SMASS Sellers, IRVING, TX, U.S.A.
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Da: SMASS Sellers, IRVING, TX, U.S.A.
Condizione: New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
Da: GreatBookPrices, Columbia, MD, U.S.A.
Condizione: New.
Da: INDOO, Avenel, NJ, U.S.A.
EUR 106,38
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EUR 102,94
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Aggiungi al carrelloCondizione: New. pp. vi + 258.
Lingua: Inglese
Editore: John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Da: Grand Eagle Retail, Bensenville, IL, U.S.A.
Prima edizione
Hardcover. Condizione: new. Hardcover. 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. 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. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 117,27
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Da: GreatBookPricesUK, Woodford Green, Regno Unito
EUR 132,22
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Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: Mispah books, Redhill, SURRE, Regno Unito
EUR 122,70
Quantità: 1 disponibili
Aggiungi al carrelloHardcover. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
Da: GreatBookPrices, Columbia, MD, U.S.A.
Condizione: As New. Unread book in perfect condition.
Da: Ubiquity Trade, Miami, FL, U.S.A.
EUR 154,70
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Da: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irlanda
Prima edizione
EUR 142,42
Quantità: 15 disponibili
Aggiungi al carrelloCondizione: New. 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. Editor(s): Lodola, Alberto; Stadler, Jeanne. Num Pages: 258 pages, Illustrations. BIC Classification: MMGT. Category: (P) Professional & Vocational. Dimension: 236 x 165 x 19. Weight in Grams: 512. . 2011. 1st Edition. Hardcover. . . . .
Condizione: New. 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. Editor(s): Lodola, Alberto; Stadler, Jeanne. Num Pages: 258 pages, Illustrations. BIC Classification: MMGT. Category: (P) Professional & Vocational. Dimension: 236 x 165 x 19. Weight in Grams: 512. . 2011. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.
Lingua: Inglese
Editore: John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Da: CitiRetail, Stevenage, Regno Unito
Prima edizione
EUR 143,53
Quantità: 1 disponibili
Aggiungi al carrelloHardcover. Condizione: new. Hardcover. 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. 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. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
EUR 140,20
Quantità: Più di 20 disponibili
Aggiungi al carrelloGebunden. Condizione: New. 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 .
Da: UK BOOKS STORE, London, LONDO, Regno Unito
EUR 200,95
Quantità: 17 disponibili
Aggiungi al carrelloCondizione: New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.
Lingua: Inglese
Editore: John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Da: AussieBookSeller, Truganina, VIC, Australia
Prima edizione
EUR 207,48
Quantità: 1 disponibili
Aggiungi al carrelloHardcover. Condizione: new. Hardcover. 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. 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. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.