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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...
- 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...
- 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...
- CRC Press 2005; US$ 167.95
Historical Development of Dissolution Testing. Compendial Testing Equipment: Calibration, Qualification, and Sources of Error. Compendial Requirements of Dissolution Testing. The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective. Physiological Parameters Relevant to Dissolution Testing: Composition of Fluids... more...
- CRC Press 2003; US$ 209.95
Regulatory basis for process validation, John M. Dietrick and Bernard T. Loftus; prospective process validation, Allen Y. Chao, F. St Forbes, and Reginald F. Johnson; retrospective process validation, Chester J. Trubinski; sterilization validation, Michael J. Akers and Neil R. Anderson; validation of solid dosage forms, Jeffrey S. Rudolph and Robert... more...
- CRC Press 2003; US$ 159.95
Principles and theory: principles of capillary electrophoresis; theory of affinity electrophoresis. Application of affinity capillary electrophoresis in pharmaceutics: determination of physicochemical parameters; affinity of drugs to excipients; affinity of drugs to pharmaceutical vehicle systems - micelles. Application of affinity capillary electrophoresis... more...
- Elsevier Science 2013; US$ 72.95
Membrane Electrodes in Drug-Substances Analysis discusses the analytical control of drugs using ion-selective membrane electrodes. This book is divided into three parts, comprised of 18 chapters organized according to the topics they cover. The first part covers the general aspects of membrane electrodes, which includes topics such as theoretical... more...