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Most popular at the top
- Wiley 2009; US$ 144.00
Drug Efficacy, Safety, and Biologics Discovery: Emerging Technologies and Tools covers key emerging technologies in pharmaceutical R & D and how they have substantially impacted (or are currently impacting) drug discovery. The cross-disciplinary collaborations implicit in integrating these technologies with drug discovery operations will... more...
- Springer 2008; US$ 89.99
Die pharmazeutische Industrie weist gegenüber anderen Branchen einige Besonderheiten auf, die in der allgemeinen Industriebetriebslehre nicht ausreichend berücksichtigt werden. Das vorliegende Buch befasst sich daher mit den speziellen volkswirtschaftlichen und betriebswirtschaftlichen Aspekten der pharmazeutischen Industrie. Neueinsteigern in diese... more...
- Springer 2011; US$ 279.00
This book features a special subsection of Nanomedicine, an application of nanotech nology to achieve breakthroughs in healthcare. It exploits the improved and often novel physical, chemical and biological properties of materials only existent at the nanometer scale. As a consequence of small scale, nanosystems in most cases are efficiently uptaken... more...
- Springer 2010; US$ 489.00
In the view of most experts pharmacology is on drugs, targets, and actions. In the context the drug as a rule is seen as an active pharmaceutical ingredient and not as a complex mixture of chemical entities of a well defined structure. Today, we are becoming more and more aware of the fact that delivery of the active compound to the target site is... more...
- Royal Society of Chemistry 2011; US$ 160.00
The modern synthetic chemist applies all the tools available to identify the drug-like molecules with the best chances of becoming novel drugs. This book will act as a primer for graduates and postgraduates interested in a career in drug discovery. It covers both synthetic technologies currently impacting medicinal chemistry and emerging areas. The... more...
- Taylor and Francis 2005; US$ 189.95
A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the... more...
- Taylor and Francis 2007; US$ 159.95
With the advent of analytical techniques and capabilities to measure particle sizes in nanometer ranges, there has been tremendous interest in the use of nanoparticles for more efficient methods of drug delivery. Nanoparticulate Drug Delivery Systems addresses the scientific methodologies, formulation, processing, applications, recent trends, and... more...
- Taylor and Francis 2011; US$ 154.95
Written to help companies comply with GMP, GLP, and validation requirements imposed by the FDA and regulatory bodies worldwide, Quality Control Training Manual: Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories presents cost-effective training courses that cover how to apply advances in the life sciences... more...
- Springer 2013; US$ 209.00
This comprehensive book encompasses various facets of sterile product development. Key concepts relevant to the successful development of sterile products are illustrated through case studies and are covered under three sections in this book: â?¢ Formulation approaches that discuss a variety of dosage forms including protein therapeutics, lipid-based... more...
- Taylor and Francis 2005; US$ 299.95
Applying basic theories to industrial practices in pharmaceutical development, this Second Edition explains how new and emerging technologies are utilized in the production of pharmaceutical granulation-demonstrating cost-effective strategies to manufacture solid-dosage forms with consistent physical properties while complying with current regulatory... more...