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Idioma: Inglés
Publicado por John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Librería: Grand Eagle Retail, Bensenville, IL, Estados Unidos de America
Original o primera edición
EUR 131,33
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Añadir al carritoHardcover. Condición: 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.
Librería: GreatBookPricesUK, Woodford Green, Reino Unido
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Idioma: Inglés
Publicado por John Wiley and Sons Ltd, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Librería: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irlanda
Original o primera edición
EUR 142,42
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Añadir al carritoCondición: 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. . . . .
Idioma: Inglés
Publicado por John Wiley and Sons Ltd, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Librería: Kennys Bookstore, Olney, MD, Estados Unidos de America
EUR 177,18
Cantidad disponible: 15 disponibles
Añadir al carritoCondición: 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.
Idioma: Inglés
Publicado por John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Librería: CitiRetail, Stevenage, Reino Unido
Original o primera edición
EUR 143,53
Cantidad disponible: 1 disponibles
Añadir al carritoHardcover. Condición: 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
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Añadir al carritoGebunden. Condición: 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 .
Librería: UK BOOKS STORE, London, LONDO, Reino Unido
EUR 200,95
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Añadir al carritoCondición: 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.
Idioma: Inglés
Publicado por John Wiley & Sons Inc, New York, 2011
ISBN 10: 0470371374 ISBN 13: 9780470371374
Librería: AussieBookSeller, Truganina, VIC, Australia
Original o primera edición
EUR 207,48
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Añadir al carritoHardcover. Condición: 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.