Основной контент книги Formulation and Analytical Development for Low-Dose Oral Drug Products
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Volume 492 pages
Formulation and Analytical Development for Low-Dose Oral Drug Products
$168
About the book
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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Age restriction:
0+Release date on Litres:
21 August 2019Volume:
492 p. ISBN:
9780470386354Total size:
6.9 МБTotal number of pages:
492Copyright holder:
John Wiley & Sons Limited