Author:
Edition: 1
Publisher: Wiley
Binding: Hardcover
ISBN: 047044861X
Pediatric Non-Clinical Drug Testing: Principles, Requirements, and Practice
This book explains the importance and practice of pediatric drug testing for pharmaceutical and toxicology professionals. Medical books Pediatric Non-Clinical Drug Testing. Medical books Pediatric Non-Clinical Drug Testing Ebook. Buy Pediatric Non-Clinical Drug Testing by and Read this Book on Kobo's Free Apps. Discover Kobo's Vast Collection of Ebooks Today - Over 3 Million Titles, Including 2 Million Free Ones!
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Buy Pediatric Non-Clinical Drug Testing by and Read this Book on Kobo's Free Apps. Discover Kobo's Vast Collection of Ebooks Today - Over 3 Million Titles, Including 2 Million Free Ones!
Store Search search Title, ISBN and Author Pediatric Non-clinical Drug Testing by Alan M. Hoberman, Elise M. Lewis Estimated delivery 3-12 business days Format Hardcover Condition Brand New After more than forty years, ethical, political and practical concerns continue to plague pediatric testing and labeling. This book explores ways to meet FDA guidelines for non-clinical testing, differences resulting from new EMEA legislation, how to develop appropriate information for submission to both age
"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 off
"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 off
Medical Book Pediatric Non-Clinical Drug Testing
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.
