Formulation and analytical development for low-dose oral drug products /
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...
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| Other Authors: | |
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| Format: | Electronic eBook |
| Language: | English |
| Published: |
Hoboken, N.J. :
John Wiley & Sons,
©2009.
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| Subjects: | |
| Online Access: | CONNECT |
| Summary: | 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. |
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| Item Description: | Wiley EBA |
| Physical Description: | 1 online resource (xxiii, 461 pages) : illustrations |
| Bibliography: | Includes bibliographical references and index. |
| ISBN: | 9780470386361 0470386363 9780470386354 0470386355 1282031058 9781282031050 9786612031052 6612031050 |
