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- Taylor and Francis 2007; 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 2001; 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 2006; 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 2014; US$ 125.00
Provides a comprehensive review of all types of medical therapeutic delivery solutions from traditional pharmaceutical therapy development to innovative medical device therapy treatment to the recent advances in cellular and stem cell therapy development • Provides information to potentially allow future development of treatments with greater... 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...
- Taylor and Francis 2008; US$ 139.95
Encompassing the full spectrum of project management?s role and responsibility encountered in the pharmaceutical industry, Pharmaceutical Project Management outlines the key objectives, risks, and challenges of each stage of the pharmaceutical lifecycle, from discovery and preclinical phases through clinical development, manufacturing, registration,... more...
- Taylor and Francis 1995; US$ 169.95
One of the most rapidly growing areas in pharmaceutical technology, the targeting of drugs via drug delivery systems offers the promise of reduced toxicity as well as more efficient and cost-effective treatment of disease. Drug Delivery Systems provides the most complete coverage available of this new and increasingly important field of study. more...