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- Springer New York 2009; US$ 219.00
Various chapters in the book are written by authors from academia, regulatory agencies and industries who are experts in their respective fields. The book includes over 600 bibliographic citations, numerous tables and illustrations. more...
- Springer New York 2013; US$ 99.00
Explains the basic science and the applications of biotechnology-derived pharmaceuticals Serves as a complete one-stop source for undergraduate pharmacists, pharmaceutical science students, and for those in the pharmaceutical industry Includes additional coverage on the newer approaches more...
- Springer US 2011; US$ 209.00
Volume focused entirely on sample preparation and extraction of pharmaceutical dosage forms A valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug product Presents multiple examples and case studies to highlight various potential issues and solutions more...
- CRC Press 2008; US$ 179.95
During the onset of any clinical trial there are many factors and variables to consider. Funding, time restraints, and regulatory agency guidelines are factors that often influence which variables will be studied, leaving other important information out of the study. Preformulation in Solid Dosage Form Development covers every topic of critical... more...
- Elsevier Science 2011; US$ 205.00
This book offers pertinent basic science information on strategies used for the rational design and discovery of novel anticancer agents, and, in addition, translational studies involving clinical trial design and execution with these novel, mostly cytostatic agents. This book covers basic science strategies that are being used in drug discovery and... more...
- Taylor and Francis 2007; US$ 199.95
Completely revised and updated to reflect the significant advances in pharmaceutical production and regulatory expectations, this third edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and competitive. The many chapters added to the prior compilation examine validation... more...
- Wiley 2006; US$ 255.00
This timely and original handbook paves the way to success in plant-based drug development, systematically addressing the issues facing a pharmaceutical scientist who wants to turn a plant compound into a safe and effective drug. Plant pharmacologists from around the world demonstrate the potentials and pitfalls involved, with many of the studies and... more...
- Wiley 2011; US$ 153.00
Discusses chiral separations and offers guidance for selecting the optimum method for desired results Chiral separations represent the most intriguing and, by some measures, most difficultseparations of chemical compounds. This book provides researchers and students an under-standing of chiral separations and offers a convenient route to selecting... more...
- Elsevier Science 2003; US$ 335.00
The United States Food and Drug Administration (FDA) and other regulatory bodies around the world require that impurities in drug substance and drug product levels recommended by the International Conference on Harmonisation (ICH) be isolated and characterized. Identifying process-related impurities and degradation products also helps us to understand... more...
- Elsevier Science 2005; US$ 295.00
High pressure liquid chromatography?frequently called high performance liquid chromatography (HPLC or, LC) is the premier analytical technique in pharmaceutical analysis and is predominantly used in the pharmaceutical industry. Written by selected experts in their respective fields, the Handbook of Pharmaceutical Analysis by HPLC Volume 6 , provides... more...