Comprehensive Guide to Toxicology in Preclinical Drug Development
- 25 %
Der Artikel wird am Ende des Bestellprozesses zum Download zur Verfügung gestellt.

Comprehensive Guide to Toxicology in Preclinical Drug Development

 EPUB
| Lieferzeit:3-5 Tage I

Unser bisheriger Preis:ORGPRICE: 184,45 €

Jetzt 137,55 €*

ISBN-13:
9780123878168
Einband:
EPUB
Seiten:
1024
Autor:
Ali S. Faqi
eBook Typ:
Adobe Digital Editions
eBook Format:
EPUB
Kopierschutz:
Adobe DRM [Hard-DRM]
Sprache:
Englisch
Beschreibung:

A Comprehensive Guide to Toxicology in Preclinical Drug Development is a resource for toxicologists in industry and regulatory settings, as well as directors working in contract resource organizations, who need a thorough understanding of the drug development process. Incorporating real-life case studies and examples, the book is a practical guide that outlines day-to-day activities and experiences in preclinical toxicology. This multi-contributed reference provides a detailed picture of the complex and highly interrelated activities of preclinical toxicology in both small molecules and biologics. The book discusses discovery toxicology and the international guidelines for safety evaluation, and presents traditional and nontraditional toxicology models. Chapters cover development of vaccines, oncology drugs, botanic drugs, monoclonal antibodies, and more, as well as study development and personnel, the role of imaging in preclinical evaluation, and supporting materials for IND applications. By incorporating the latest research in this area and featuring practical scenarios, this reference is a complete and actionable guide to all aspects of preclinical drug testing.Chapters written by world-renowned contributors who are experts in their fieldsIncludes the latest research in preclinical drug testing and international guidelinesCovers preclinical toxicology in small molecules and biologics in one single source
A Comprehensive Guide to Toxicology in Preclinical Drug Development is a resource for toxicologists in industry and regulatory settings, as well as directors working in contract resource organizations, who need a thorough understanding of the drug development process. Incorporating real-life case studies and examples, the book is a practical guide that outlines day-to-day activities and experiences in preclinical toxicology. This multi-contributed reference provides a detailed picture of the complex and highly interrelated activities of preclinical toxicology in both small molecules and biologics. The book discusses discovery toxicology and the international guidelines for safety evaluation, and presents traditional and nontraditional toxicology models. Chapters cover development of vaccines, oncology drugs, botanic drugs, monoclonal antibodies, and more, as well as study development and personnel, the role of imaging in preclinical evaluation, and supporting materials for IND applications. By incorporating the latest research in this area and featuring practical scenarios, this reference is a complete and actionable guide to all aspects of preclinical drug testing.Chapters written by world-renowned contributors who are experts in their fieldsIncludes the latest research in preclinical drug testing and international guidelinesCovers preclinical toxicology in small molecules and biologics in one single source