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|a Pharmaceutical Analysis
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|a Hoboken
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|a Half title; Series title; Title; Contents; Contributors; Preface; 1 Quality control and regulation, C.J. Moores; 2 Development of achiral separation methods in pharmaceutical analysis, George N. Okafo and John K. Roberts; 3 Chiral analysis of pharmaceuticals, W. John Lough; 4 Nuclear magnetic resonance spectroscopy in pharmaceutical analysis, Richard J. Smith and Andrew J. Edwards; 5 Mass spectrometry in pharmaceutical analysis, Neville Haskins; 6 Vibrational spectroscopy in pharmaceutical analysis, Clare L. Anderton
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| 505 |
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|a 7 Solid-state analysis and polymorphism, Ulrich J. Griesser and Joseph G. Stowell8 Microscopy and imaging in pharmaceutical analysis, Robert A. Carlton; 9 Process analysis in the pharmaceutical industry, Martin Warman and Steve Hammond; Index;
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| 520 |
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|a The use of analytical sciences in the discovery, development and manufacture of pharmaceuticals is wide-ranging. From the analysis of minute amounts of complex biological materials to the quality control of the final dosage form, the use of analytical technology covers an immense range of techniques and disciplines. This book concentrates on the analytical aspects of drug development and manufacture, focusing on the analysis of the active ingredient or drug substance. It provides those joining the industry or other areas of pharmaceutical research with a source of reference to a broad range
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