[PDF.21zh] New Drug Development: A Regulatory Overview (NEW DRUG DEVELOPMENT ( MATHIEU))

New Drug Development: A Regulatory Overview (NEW DRUG DEVELOPMENT ( MATHIEU))

[PDF.wq26] New Drug Development: A Regulatory Overview (NEW DRUG DEVELOPMENT ( MATHIEU))

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 | #320224 in Books |  Parexel International Corporation |  2005-05 | Original language:English | PDF # 1 |  11.00 x8.50 x1.00l, | File type: PDF | 389 pages

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||3 of 4 people found the following review helpful.| Regulatory Affairs Textbook Standard|By Catherine V. Velazquez|The book is a comprehensive collection of Regulatory Affairs information. The book lacks an index. Thankfully, the table of contents is detailed enough to find most of the information one might be looking for.|2 of 5 people found the following review helpful.| $189.00????|B

Go inside the drug development and FDA regulatory process with today's most authoritative and popular reference on the topic. In its all-new 2008 edition, New Drug Development: A Regulatory Overview addresses the most cutting-edge developments redefining how new drugs are developed and regulated today, including:

* How the FDA Amendments Act of 2007 will affect everything from drug reviews to postmarketing requirements.

* How the CDER's efforts to integrate...

You can specify the type of files you want, for your device.New Drug Development: A Regulatory Overview (NEW DRUG DEVELOPMENT ( MATHIEU))   |  Mark P. Mathieu, Anne G. Evans. A good, fresh read, highly recommended.

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