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A Comprehensive Guide to Toxicology in Nonclinical Drug Development, Second Edition, is a valuable reference designed to provide a complete;
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central to drug development. The chapters provide an understanding of the key components of the preclinical phase of drug development with a hands;
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in Nonclinical Safety Assessment is written by experts who have direct, firsthand involvement in drug development in the regions where they are located;
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in its own right. This text brings together for the first time in a single volume a comprehensive survey of methods important to the nonclinical;
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, bioinformatics and machine learning approaches with nonclinical and clinical experimentation to accelerate drug development. This book discusses the;
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, bioinformatics and machine learning approaches with nonclinical and clinical experimentation to accelerate drug development. This book discusses the;
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risk factors before a drug is put to market. The book covers both clinical and nonclinical aspects for understanding drug-drug interactions as;
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The Nonhuman Primate in Drug Development and Safety Assessment is a valuable reference dedicated to compiling the latest;
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of histopathological lesions observed in drug development. In addition, it will provide information to assist the pathologist in making determinations of the;
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As a guide for pharmaceutical professionals to the issues and practices of drug discovery toxicology, this book integrates and reviews the;
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The purpose of this third edition of Developmental and Reproductive Toxicology is to provide a practical guide to developmental and;
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modeling and simulation in drug development, a review of ICH preclinical guidelines, and experimental methods used to study membrane drug transport;
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Explaining the assessment of potential drug compounds, this is an ideal introductory reference for those new to drug discovery. It includes;
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, Resolving Erroneous Reports in Toxicology and Therapeutic Drug Monitoring provides an up-to-date introduction to the tests and methodologies used;
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in nonclinical toxicology studies designed to detect potential human toxicity of drugs, agrochemicals, industrial chemicals, and environmental hazards;
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relating to drug and toxin exposures. Each case study includes contemporary clinical and forensic toxicologist studies that include a comprehensive;
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detecting, understanding, predicting and preventing adverse events' was a critical path to the future of drug safety. This book brings together a;
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, governmental and industrial environments, to provide a unique, comprehensive look at: - Why hair can serve as an invaluable bio-resource in toxicology;
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, does what it needs to do, and is subsequently cleared from the body, the practice of safety assessment will have to change. Nonclinical Drug;
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This publication contains a verbatim reproduction of 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies.;
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techniques at earlier stages of drug development can speed the development of a drug candidate. Written by experts who have pioneered green;
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Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the;
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This issue of Clinics in Laboratory Medicine, edited by Dr. Martin Bluth, will cover a wide array of topics related to drug testing and;
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Drug-drug interactions (DDIs) occur when a patient is exposed simultaneously to multiple pharmaceuticals, which can result in variations;
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) instrumentation for Therapeutic DrugMonitoring (TDM) and toxicology drug assays and reviews the clinical pharmacologyof major classes of drugs and their;
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Written by a leading researcher in the field, Transporters in Drug Discovery and Development provides a comprehensive and practical guide;
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