{"product_id":"pharmaceutical-toxicology-in-practice-9780470371374","title":"Pharmaceutical Toxicology in Practice","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eThis book describes, with references to key source materials,the background to, and conduct of, the principal nonclinical studiesthat 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, andrisk management.Further, the book covers the methods of genetic toxicology (assays, genomics, in vivo screening) as a complement to traditional \u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\"So, overall, this is a wonderful book for all those who want to learn more about pharmaceutical toxicology and for those who start working in the field.\" (The British Toxicology Society, 1 May 2011)  \u003cp\u003e \"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\". (Quote.com, 19 January 2011)\u003c\/p\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cb\u003eCONTRIBUTORS.\u003c\/b\u003e  \u003cp\u003eChapter 1: Introduction (\u003ci\u003eAlberto Lodola and Jeanne Stadler\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 2: The Regulatory Environment (\u003ci\u003eClaudio Bernardi and Marco Brughera\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 3: Toxicological development: Roles and Responsibilities (\u003ci\u003eFranck Chuzel and Bernard Ruty\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 4: Contract Research Organizations (\u003ci\u003eMaurice Cary\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 5: Safety Pharmacology (\u003ci\u003eClaudio Arrigoni and Valeria Perego\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 6: Formulations, Impurities and Toxicokinetics (\u003ci\u003eClaude Charuel\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 7: General Toxicology (\u003ci\u003eAlberto Lodola\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 8: Genetic Toxicology (\u003ci\u003ePeggy Guzzie-Peck, Jennifer Sasaki and Sandy Weiner\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 9: Developmental and reproductive toxicology (\u003ci\u003eJeanne Stadler\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 10: Data analysis, report writing and regulatory documentation (\u003ci\u003eMonique Y. Wells\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003eChapter 11: Risk Management (\u003ci\u003eAlberto Lodola\u003c\/i\u003e).\u003c\/p\u003e \u003cp\u003e\u003cb\u003eINDEX.\u003c\/b\u003e\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49525370356055,"sku":"9780470371374","price":96.5,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780470371374.jpg?v=1731860261","url":"https:\/\/bookcurl.com\/products\/pharmaceutical-toxicology-in-practice-9780470371374","provider":"Book Curl","version":"1.0","type":"link"}