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Most popular at the top
- Springer New York 2008; US$ 169.99
This handbook is the first to cover all aspects of stability testing in pharmaceutical development. Written by a group of international experts, the book presents a scientific understanding of regulations and balances methodologies and best practices. more...
- Springer Milan 2009; US$ 17.85
Le droghe vegetali, a differenza dei farmaci di sintesi (o artificiali), contengono piů sostanze farmacologicamente attive: tra queste si stabiliscono dei sinergismi e degli antagonismi che caratterizzano l?azione terapeutica del preparato vegetale (fitoterapico). Tuttavia, per molte droghe vegetali queste interazioni non sono state ancora del tutto... more...
- IOS Press 2009; US$ 159.00
The number of novel medications in the global industry pipeline is insufficient to suffice demand of the markets, the financial performance of several companies is declining, and sales and marketing costs are rising. This title addresses the development in synthetic and medicinal chemistry with the emphasis on global challenges. more...
- Wiley 2013; US$ 140.00 US$ 121.33
Compatibility of Pharmaceutical Products and Contact Materials Dennis Jenke Important safety aspects of compatibility for therapeutic products and their manufacturing systems, delivery devices, and containers Compatibility of Pharmaceutical Products and Contact Materials helps pharmaceutical, toxicology, analytical, and regulatory affairs professionals... more...
- BRILL 2007; US$ 175.00
This book offers a critical Arabic edition, annotated English translation, introductory study, and two-way glossaries of a pharmacological masterpiece composed around the middle of the 12th century CE in Baghdad by the Nestorian physician Ibn at-Tilm??. more...
- Wiley 2009; US$ 140.00 US$ 121.33
A consolidated and comprehensive reference on ligand-binding assays Ligand-binding assays (LBAs) stand as the cornerstone of support for definition of the pharmaco-kinetics and toxicokinetics of macromolecules, an area of burgeoning interest in the pharmaceutical industry. Yet, outside of the Crystal City Conference proceedings, little guidance... more...
- Wiley 2006; US$ 305.00 US$ 264.33
This handbook provides the first-ever inside view of today's integrated approach to rational drug design. Chemoinformatics experts from large pharmaceutical companies, as well as from chemoinformatics service providers and from academia demonstrate what can be achieved today by harnessing the power of computational methods for the drug discovery process.... more...
- Wiley 2006; US$ 309.00 US$ 267.80
The new edition of this practice-oriented handbook features thoroughly updated contents, including recent developments in parallel synthesis. A new chapter on screening complements the overview of combinatorial strategy and synthetic methods. "Experimental details and complete reaction data [...] are a constant theme running through this work"... more...