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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...
- 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...
- Wiley 2013; US$ 159.95 US$ 138.62
Consolidates the information LC-MS bioanalytical scientists need to analyze small molecules and macromolecules The field of bioanalysis has advanced rapidly, propelled by new approaches for developing bioanalytical methods, new liquid chromatographic (LC) techniques, and new mass spectrometric (MS) instruments. Moreover, there are a host of guidelines... more...
- CRC Press 2005; US$ 167.95
An expertly written source on the devices, systems, and technologies used in the dissolution testing of oral pharmaceutical dosage forms, this reference provides reader-friendly chapters on currently utilized equipment, equipment qualification, consideration of the gastrointestinal physiology in test design, the analysis and interpretation of data... more...
- CRC Press 2003; US$ 79.95
This reference presents the most recent breakthroughs and techniques in affinity capillary electrophoresis (ACE) to measure and determine the physicochemical and thermodynamic parameters of drug compounds. The authors offer strategies to explore and characterize interactions between drugs, drug vehicles, and biological membranes to facilitate developments... more...
- CRC Press 2001; US$ 239.95
Exploring the analysis of pharmaceuticals, including polymorphic forms, this book discusses regulatory requirements in pharmaceutical product development and pharmaceutical testing. It covers methods of drug separation and procedures such as capillary electrophoresis for chromatographic separation of molecules. Additional topics include drug formulation... more...