{
"item_title" : "Formulation and Analytical Development for Low-Dose Oral Drug Products",
"item_author" : [" Jack Zheng "],
"item_description" : "There are unique challenges in the formulation, manufacture, analytical chemistry, and regulatory requirements of low-dose drugs. This book provides an overview of this specialized field and combines formulation, analytical, and regulatory aspects of low-dose development into a single reference book. It describes analytical methodologies like dissolution testing, solid state NMR, Raman microscopy, and LC-MS and presents manufacturing techniques such as granulation, compaction, and compression. Complete with case studies and a discussion of regulatory requirements, this is a core reference for pharmaceutical scientists, regulators, and graduate students.",
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Overview
There are unique challenges in the formulation, manufacture, analytical chemistry, and regulatory requirements of low-dose drugs. This book provides an overview of this specialized field and combines formulation, analytical, and regulatory aspects of low-dose development into a single reference book. It describes analytical methodologies like dissolution testing, solid state NMR, Raman microscopy, and LC-MS and presents manufacturing techniques such as granulation, compaction, and compression. Complete with case studies and a discussion of regulatory requirements, this is a core reference for pharmaceutical scientists, regulators, and graduate students.
This item is Non-Returnable
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Details
- ISBN-13: 9780470056097
- ISBN-10: 0470056096
- Publisher: Wiley
- Publish Date: February 2009
- Dimensions: 9.3 x 6.2 x 1.1 inches
- Shipping Weight: 1.75 pounds
- Page Count: 500
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