Pediatric Non-Clinical Drug Testing: Principles, Requirements, and Practice - Hardcover

Hardcover

ISBN 10: 047044861X ISBN 13: 9780470448618

Publisher: Wiley, 2012

Synopsis

This book explains the importance and practice of pediatric drug testing for pharmaceutical and toxicology professionals. It describes the practical and ethical issues regarding non-clinical testing to meet US FDA Guidelines, differences resulting from the new European EMEA legislation, and how to develop appropriate information for submission to both agencies. It also provides practical study designs and approaches that can be used to meet international requirements. Covering the full scope of non-clinical testing, regulations, models, practice, and relation to clinical trials, this text offers a comprehensive and up-to-date resource.

About this title

About the Author

ALAN M. HOBERMAN, PhD, DABT, Fellow ATS, is Executive Director of Site Operations and Toxicology at Charles River Preclinical Services, Horsham, PA.

ELISE M. LEWIS, PhD, is Director of Reproductive and Neurobehavioral Toxicology at Charles River Preclinical Services, Horsham, PA.

From the Back Cover

Enables readers to successfully perform non-clinical drug testing, meeting international requirements

Although the non-clinical and clinical testing needs of drugs for pediatric populations have been discussed and debated for more than forty years, many ethical, political, and practical issues remain unresolved, making pediatric drug testing and labeling a challenge for pharmaceutical and toxicology professionals. Written and edited by a team of leading international experts, this book explains both the importance and the practice of non-clinical pediatric drug testing. Moreover, it guides readers through the complex set of international rules and regulations governing the practice today.

Following the authors' clear advice, readers will be able to meet FDA guidelines for non-clinical pediatric drug testing, from initial study design to submission of results for approval. Moreover, the authors describe key differences between the FDA guidelines and European Medicines Agency (EMA) legislation, enabling readers to devise and conduct studies, analyze the results, and then compile appropriate information for submission to both agencies.

Pediatric Non-Clinical Drug Testing offers clear guidance for managing the key challenges of non-clinical testing models, helping readers overcome the difficulties associated with:

• Lack of fully comparable models

• Inadequate historical experience

• Specific needs and effects associated with testing animals

• Practical problems using the clinical route of exposure in animal models

The book's appendix features a sample juvenile toxicity testing protocol that readers can use as a template for their own experimental designs.

In addition to toxicologists and pharmacokineticists, this book is recommended for drug regulators who need to develop and enforce drug testing standards to protect children. It is also recommended as a textbook for toxicology and pediatric medicine courses.

Although the non-clinical and clinical testing needs of drugs for pediatric populations have been discussed and debated for more than forty years, many ethical, political, and practical issues remain unresolved, making pediatric drug testing and labeling a challenge for pharmaceutical and toxicology professionals. Written and edited by a team of leading international experts, this book explains both the importance and the practice of non-clinical pediatric drug testing. Moreover, it guides readers through the complex set of international rules and regulations governing the practice today.

Following the authors' clear advice, readers will be able to meet FDA guidelines for non-clinical pediatric drug testing, from initial study design to submission of results for approval. Moreover, the authors describe key differences between the FDA guidelines and European Medicines Agency (EMA) legislation, enabling readers to devise and conduct studies, analyze the results, and then compile appropriate information for submission to both agencies.

Pediatric Non-Clinical Drug Testing offers clear guidance for managing the key challenges of non-clinical testing models, helping readers overcome the difficulties associated with:

• Lack of fully comparable models

• Inadequate historical experience

• Specific needs and effects associated with testing animals

• Practical problems using the clinical route of exposure in animal models

The book's appendix features a sample juvenile toxicity testing protocol that readers can use as a template for their own experimental designs.

In addition to toxicologists and pharmacokineticists, this book is recommended for drug regulators who need to develop and enforce drug testing standards to protect children. It is also recommended as a textbook for toxicology and pediatric medicine courses.

Edition details

• Publisher: Wiley
• Publication date: 2012
• Language: English
• ISBN 10: 047044861X
• ISBN 13: 9780470448618
• Binding: Hardcover
• Edition number: 1
• Number of pages: 384
• Editor: Hoberman Alan M., Lewis Elise M.