9781118949658 - Metabolite Safety in Drug Development (20 resultados)

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Hardcover. Condición: new. Hardcover. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Reviews the analytical techniques and experimental designs critical for metabolite studies Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

Hardback. Condición: New. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA.    Reviews the analytical techniques and experimental designs critical for metabolite studies.    Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation.    Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions.    Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines.

Hardcover. Condición: New.

Condición: New. pp. 608.

Couverture rigide. Condición: Comme neuf. Edition originale. Paris 2016. 1 Volume/1. - Hardback - 352 pages ************************** '' A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. . Reviews the analytical techniques and experimental designs critical for metabolite studies . Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation . Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions . Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines.

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Condición: New. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Editor(s): Iverson, Suzanne L.; Smith, Dennis A. Num Pages: 352 pages. BIC Classification: TDCW. Category: (P) Professional & Vocational. Dimension: 242 x 158 x 23. Weight in Grams: 618. . 2016. Hardcover. . . . .

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Condición: New. pp. 608.

Hardcover. Condición: new. Hardcover. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Reviews the analytical techniques and experimental designs critical for metabolite studies Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Condición: As New. Unread book in perfect condition.

Hardcover. Condición: Brand New. 1st edition. 352 pages. 9.25x6.25x0.75 inches. In Stock.

Hardback. Condición: New. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA.    Reviews the analytical techniques and experimental designs critical for metabolite studies.    Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation.    Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions.    Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines.

Condición: New. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Editor(s): Iverson, Suzanne L.; Smith, Dennis A. Num Pages: 352 pages. BIC Classification: TDCW. Category: (P) Professional & Vocational. Dimension: 242 x 158 x 23. Weight in Grams: 618. . 2016. Hardcover. . . . . Books ship from the US and Ireland.

Hardcover. Condición: new. Hardcover. A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Reviews the analytical techniques and experimental designs critical for metabolite studies Covers methods including chirality, species differences, mass spectrometry, radiolabels, and in vitro / in vivo correlation Discusses target pharmacology, in vitro systems aligned to toxicity tests, and drug-drug interactions Includes perspectives from authors with firsthand involvement in industry and the study of drug metabolites, including viewpoints that have influenced regulatory guidelines A reference on drug metabolism and metabolite safety in the development phase, this book reviews the analytical techniques and experimental designs critical for metabolite studies. It features case studies of lessons learned and real world examples, along with regulatory perspectives from the US FDA and EMA. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.