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A comprehensive guide to toxicology in nonclinical drug development /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Faqi, Ali S. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London, United Kingdom : Academic Press is an imprint of Elsevier, [2016]
Edición:Second edition.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 2 |a A comprehensive guide to toxicology in nonclinical drug development /  |c edited by Ali Said Faqi. 
250 |a Second edition. 
264 1 |a London, United Kingdom :  |b Academic Press is an imprint of Elsevier,  |c [2016] 
264 4 |c �2017 
300 |a 1 online resource (xiii, 971 pages) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Includes index. 
588 0 |a Online resource; title from PDF title page (ScienceDirect, viewed November 22, 2016). 
505 0 |a 1. Introduction; 2. ADME in Drug Discovery; 3. Pharmacokinetics and Toxicokinetics; 4. Acute, Sub-Acute, Sub-Chronic and Chronic, Dermal and Inhalation Toxicology; 5. Contemporary Practices in Core Safety Pharmacology Assessments; 6. Genetic Toxicology Testing; 7. Clinical Pathology; 8. Best Practice in Toxicologic Pathology; 9. Molecular Pathology: Applications in Nonclinical Drug Development; 10. Infusion Toxicology and Techniques; 11. The Preparation of a Nonclinical Dossier to Support an Investigational New Drug (IND) Application and First-in-Human Clinical Trials; 12. Developmental and Reproductive Toxicology; 13. Immunotoxicology Assessment in Drug Development; 14. Juvenile Toxicity Testing to Support Clinical Trials in the Pediatric Population; 15. Photosafety: Current Methods and Future Direction; 16. Dermal Toxicology; 17. Inhalation Toxicology; 18. 
505 0 |a Nonclinical Evaluation of Carcinogenicity using the Rodent Two-Year Bioassay and Carcinogenicity Evaluations using Genetically Engineered Animals; 19 Current Strategies for Abuse Liability Assessment of New Chemical Entities; 20. Nonclinical Development of Monoclonal Antibodies; 21. Nonclinical Development of Non-Oncogenic Drugs (Small and Large Molecules); 22. Nonclinical Development of Oncology Drugs; 23. Safety Evaluation of Ocular Drugs; 24. Nonclinical toxicology of Vaccines; 25. Stem Cells In Nonclinical Toxicology; 26. Overview of the Nonclinical Development Strategies and Class-Effects of Oligonucleotide-Based Therapeutics; 27. Nonclinical Safety Assessment of Botanical Drugs; 28. Regulatory Toxicology; 29. Biostatistics for Toxicologists; 30. Role of Study Director and Study Monitor in Drug Development; 31. Use of Imaging for Nonclinical Evaluation; 32. Biomarkers in Toxicology; 33. Predictive Toxicology: Biological Assay Platforms; 34. 
505 0 |a Toxicometabolomics: Technology and Applications; 35. Toxicogenomics in Nonclinical Development; 36. Nonclinical Testing of Medical Devices; 37. The Pitfalls of Drug Development 
650 0 |a Drugs  |x Toxicology. 
650 0 |a Drug development. 
650 6 |a M�edicaments  |x Toxicologie.  |0 (CaQQLa)201-0007218 
650 6 |a M�edicaments  |x D�eveloppement.  |0 (CaQQLa)201-0306620 
650 7 |a MEDICAL  |x Pharmacology.  |2 bisacsh 
650 7 |a Drug development  |2 fast  |0 (OCoLC)fst00898670 
650 7 |a Drugs  |x Toxicology  |2 fast  |0 (OCoLC)fst00898958 
700 1 |a Faqi, Ali S.,  |e editor. 
776 0 8 |i Print version:  |t Comprehensive guide to toxicology in nonclinical drug development.  |b Second edition.  |d London, United Kingdom : Academic Press is an imprint of Elsevier, [2016]  |z 0128036206  |z 9780128036204  |w (OCoLC)942707459 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128036204  |z Texto completo