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- iSmithers Rapra Publishing 2006; US$ 460.00
Pharmaceutical packaging can pose a serious problem for manufacturers. As legislation on the display of ingredients, side effects and safety warnings increases, the demands on the labelling and packaging become extreme. This can lead to pages of instructions and disclaimers included in the pack to meet regulations and cover pharmaceutical companies... more...
- Taylor and Francis 2014; US$ 159.95
Since the completion of the first edition of this book, major developments have occurred in the pharmaceutical industry that have shaped the field of near-infrared (NIR) spectroscopy. A new initiative from the U.S. Food and Drug Administration (FDA) to modernize regulations of pharmaceutical manufacturing and drug quality has helped position NIR spectroscopy... more...
- Taylor and Francis 2004; US$ 220.00
Recent years have seen a greater industrial emphasis in undergraduate and postgraduate courses in the pharmaceutical and chemical sciences. However, textbooks have been slow to adapt, leaving the field without a text/reference that is both instructional and practical in the industrial setting ? until now. A Handbook of Bioanalysis and Drug Metabolism... more...
- World Health Organization 2008; US$ 30.00
The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for medicines' quality assurance. Standards are developed by the Committee through worldwide consultation and an international consensus building process. The forty-second meeting adopted 11 new monographs... more...
- PharmaMed Press 2009; US$ 50.00
"Analysis of drugs and pharmaceuticals forms the backbone of research and development in Pharmaceutical industry and Academia. This book focuses on various Physico-Chemical and instrumental techniques and their wider application for large number of drugs. The book is conveniently divided into several chapters, each chapter dealing with a method... more...
- Springer 2010; US$ 219.00
"New Drug Development: Second Edition" provides an overview of the design concepts and statistical practices involved in therapeutic drug development. This wide spectrum of activities begins with identifying a potentially useful drug candidate that can perhaps be used in the treatment or prevention of a condition of clinical concern, and... more...
- World Health Organization 2009; US$ 40.00
The Expert Committee on Specifications for Pharmaceutical Preparations gives recommendations and provides independent international standards and guidelines in the area of quality assurance for implementation by WHO Member States international organizations United Nations agencies regional and interregional harmonization efforts as well as WHO's... more...
- World Health Organization 2009; US$ 25.00
This report presents the recommendations of the WHO Expert Committee responsible for updating the WHO Model List of Essential Medicines. The first part contains a review of the report of a meeting of the Expert Subcommittee on the Selection and Use of Essential Medicines held in October 2008. It also provides details of new applications for paediatric... more...
- Bentham Science Publishers 2010; US$ 39.00
Reviews in Pharmaceutical and Biomedical Analysis - Reviews in Pharmaceutical and Biomedical Analysis contains coverage and review of new trends and applications in all areas of pharmaceutical, biomedical and analytical chemistry. Authors have contributed review articles according to their expertise on various relevant topics.The books aim is... more...
- Springer 2013; US$ 189.00
Essential Elements for a GMP Analytical Chemistry Department is a systematic approach to understanding the essential elements required for a successful GMP Analytical Department to function as an efficient and effective organization. It describes in detail a department structure which allows for the necessary processes to become available to... more...