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Pharmaceutical toxicology in practice : a guide for non-clinical development /

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 descripti...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Lodola, Alberto, Stadler, Jeanne
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Hoboken, N.J. : Wiley, ©2011.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Pharmaceutical toxicology in practice :  |b a guide for non-clinical development /  |c edited by Alberto Lodola, Jeanne Stadler. 
260 |a Hoboken, N.J. :  |b Wiley,  |c ©2011. 
300 |a 1 online resource (vi, 258 pages) :  |b illustrations 
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505 0 |a Frontmatter -- Introduction / Alberto Lodola, Jeanne Stadler -- The Regulatory Environment / Claudio Bernardi, Marco Brughera -- Toxicological Development: Roles and Responsibilities / Franck Chuzel, Bernard Ruty -- Contract Research Organizations / Maurice Cary -- Safety Pharmacology / Claudio Arrigoni, Valeria Perego -- Formulations, Impurities, and Toxicokinetics / Claude Charuel -- General Toxicology / Alberto Lodola -- Genetic Toxicology / Peggy Guzzie-Peck, Jennifer C Sasaki, Sandy K Weiner -- Developmental and Reproductive Toxicology / Jeanne Stadler -- Data Analysis, Report Writing, and Regulatory Documentation / Monique Y Wells -- Risk Management / Alberto Lodola -- Index. 
504 |a Includes bibliographical references and index. 
505 0 |a Introduction / Alberto Lodola and Jeanne Stadler -- The regulatory environment / Claudio Bernardi and Marco Brughera -- Toxicological development : roles and responsibilities / Franck Chuzel and Bernard Ruty -- Contract research organizations / Maurice Cary -- Safety pharmacology / Claudio Arrigoni and Valeria Perego -- Formulations, impurities, and toxicokinetics / Claude Charuel -- General toxicology / Alberto Lodola -- Genetic toxicology / Peggy Guzzie-Peck, Jennifer C. Sasaki, and Sandy K. Weiner -- Developmental and reproductive toxicology / Jeanne Stadler -- Data analysis, report writing, and regulatory documentation / Monique Y. Wells -- Risk management / Alberto Lodola. 
520 |a 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. 
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650 0 |a Drugs  |x Toxicity testing. 
650 0 |a Drugs  |x Side effects. 
650 2 |a Drug Evaluation, Preclinical  |x standards 
650 2 |a Drug-Related Side Effects and Adverse Reactions 
650 2 |a Toxicity Tests  |x standards 
650 6 |a Médicaments  |x Toxicité. 
650 6 |a Médicaments  |x Effets secondaires. 
650 7 |a MEDICAL  |x Pharmacology.  |2 bisacsh 
650 7 |a Drugs  |x Side effects  |2 fast 
650 7 |a Drugs  |x Toxicity testing  |2 fast 
700 1 |a Lodola, Alberto. 
700 1 |a Stadler, Jeanne. 
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776 0 8 |i Print version:  |t Pharmaceutical toxicology in practice.  |d Hoboken, N.J. : Wiley, ©2011  |z 9780470909904  |w (OCoLC)710018916 
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