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- Taylor and Francis 2013; US$ 159.95
Preformulation studies are the physical, chemical, and biological studies needed to characterize a drug substance for enabling the proper design of a drug product, whereas the effectiveness of a drug product is determined during the formulation studies phase. Though the two disciplines overlap in practice, each is a significantly distinct phase of... more...
- Taylor and Francis 2013; US$ 169.95
An invaluable source instruction on the principles, instrumentation, design, implementation, operation, and maintenance of an effective clean-in-place system (CIP), this guide illustrates best practices and successful applications of CIP in both pharmaceutical and biotechnology facilities. Offering reader-friendly descriptions of the various types... more...
- Taylor and Francis 2013; US$ 179.95
Thoroughly updated and expanded, this new Third Edition provides the latest information on dosage, forms, film defects, and polymer characterization. Written by renowned leaders in the field, Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms is easily the most comprehensive book available on the market today. New to the Third Edition... more...
- Taylor and Francis 2013; US$ 149.95
This title demonstrates how designed experiments are the most scientific, efficient, and cost effective method of data collection for validation in a laboratory setting. Intended as a learn-by-example guide, Pharmaceutical and Medical Device Validation by Experimental Design demonstrates why designed experiments are the most logical and rational approach... more...
- Taylor and Francis 2013; US$ 159.95
Increasingly, pharmaceutical scientists must not only be specialists in their field but must also be familiar with legislation that governs the use of equipment in their industry. The regulation of test and measuring equipment changes continually as new regulations are introduced and new equipment is developed. Calibration in the Pharmaceutical Laboratory... more...
- Taylor and Francis 2013; US$ 239.95
Spanning every critical element of validation for any pharmaceutical, diagnostic, medical device or equipment, and biotech product, this Second Edition guides readers through each step in the correct execution of validating processes required for non-aseptic and aseptic pharmaceutical production. With 14 exclusive environmental performance evaluations,... more...
- Wiley 2013; US$ 205.00
Systematically examining current methods and strategies, this ready reference covers a wide range of molecular structures, from organic-chemical drugs to peptides, proteins and nucleic acids, in line with emerging new drug classes derived from biomacromolecules. A leader in the field and one of the pioneers of this young discipline has assembled here... more...
- Wiley 2005; US$ 165.00
An indispensable tool for those working at the front lines of new drug development Written for busy professionals at the forefront of new drug development, Drug Delivery gets readers quickly up to speed on both the principles and latest applications in the increasingly important field of drug delivery. Recent developments in such areas as combinatorial... more...
- Springer 2007; US$ 239.00
Comprises the relevant aspects for the clinical application of biologics. This book describes the "differential therapy" with biologics namely in the fields of dermatology, rheumatology, gastroenterology, and neurology. It is intended for researchers and clinicians. more...
- Springer 2008; US$ 259.00
Multifunctional Pharmaceutical Nanocarriers intends to bring together the experts in the field of multifunctional nanopharmaceuticals to provide the reader with the cutting edge information, a critical overview of the field, and analysis of the current and future tendencies and developments to aid in the rapid developments in the field. more...