logo
Product categories

EbookNice.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link.  https://ebooknice.com/page/post?id=faq


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookNice Team

(Ebook) Safety Efforts in Pediatric Drug Development by Conor D. Byrne ISBN 9781612093680, 161209368X

  • SKU: EBN-51356196
Zoomable Image
$ 32 $ 40 (-20%)

Status:

Available

0.0

0 reviews
Instant download (eBook) Safety Efforts in Pediatric Drug Development after payment.
Authors:Conor D. Byrne
Pages:149 pages.
Year:2009
Editon:1
Publisher:Nova Science Publishers, Incorporated
Language:english
File Size:4.19 MB
Format:pdf
ISBNS:9781612093680, 161209368X
Categories: Ebooks

Product desciption

(Ebook) Safety Efforts in Pediatric Drug Development by Conor D. Byrne ISBN 9781612093680, 161209368X

This book focuses on the safety efforts being implemented in pediatric drug development. Although children suffer from many of the same diseases as adults and are often treated with the same drugs, only about one-third of the drugs that are prescribed for children have been studied and labeled for pediatric use. This has placed children taking drugs for which there have not been adequate pediatric drug studies at risk of being exposed to ineffective treatment or receiving incorrect dosing. In order to encourage the study of more drugs for pediatric use, Congress passed the Best Pharmaceuticals for Children Act (BPCA) in 2002 to provide marketing incentives to drug manufacturers for conducting pediatric drug studies. Drug manufacturers may obtain six months of additional market exclusivity for drugs on which they have conducted pediatric studies in accordance with pertinent law and regulations. This book also evaluates the impact of BPCA on labeling drugs for pediatric use and the process by which the labeling was changed, and illustrates the range of diseases treated by the drugs studied under BPCA. Additionally this book provides guidance on the role and timing of animal studies in the nonclinical safety evaluation of therapeutics intended for the treatment of pediatric patients. The guidance discusses some conditions under which juvenile animals can be meaningful predictors of toxicity in pediatric patients and makes recommendations on nonclinical testing. This book consists of public documents which have been located, gathered, combined, reformatted, and enhanced with a subject index, selectively edited and bound to provide easy access.
*Free conversion of into popular formats such as PDF, DOCX, DOC, AZW, EPUB, and MOBI after payment.

Related Products