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Most popular at the top
- iSmithers Rapra Publishing 2010; US$ 165.00
Impurities originating from any part of the manufacturing or storage of drug products can potentially result in expensive product recalls and damage to a company's reputation - not to mention the serious threat posed to patient safety. Nowadays extractables and leachables assessment of all materials - and especially elastomeric and plastic components... more...
- Bentham Science Publishers 2009; US$ 24.00
This Ebook covers the emerging and most important theories underlying artificial intelligence applications in a variety of medical problems. It is written for physicians, researchers, engineers, statisticians and advanced students who wish to increase their familiarity with different topics of modern mathematics related to predictive medicine. Both... more...
- Bentham Science Publishers 2012; US$ 39.00
This e-book explores an open problem in academic literature with a stimulating discussion on chemoinformatics with respect to neglected diseases, pointing out perspectives on using molecular modeling and theoretical approaches. It is a handy reference guide for students and advanced researchers. more...
- iSmithers Rapra Publishing 2011; US$ 165.00
The examination of extractables and leachables from materials in contact with a drug product or the patient is growing in importance due to increased regulatory scrutiny from organisations such as the Food and Drugs Administration (FDA) and the European Medicines Agency (EMEA). Regulators are concerned with the interaction of various drug delivery... more...
- Organisation for Economic Co-operation and Development 2006; US$ 63.00
What are the specific characteristics of innovation in pharmaceutical biotechnology? How do biopharmaceutical innovation systems in OECD countries perform and which policies are suitable to foster performance?. This publication examines the innovation system in pharmaceutical biotechnology in eight OECD countries - Belgium, Finland, France, Germany,... more...
- SAGE Publications 2011; US$ 144.00
This handbook aims to provide updated information on the current progress of biosimilar medicines in the European Union (EU). The first edition of this short guide to biosimilar medicines was published in 2007. At the time of first publication, only 5 biosimilar medicines had been approved in Europe, and both the legislation and concepts for these... more...
- Sage Publications Ltd. 2011; US$ 144.00
Questo manuale si propone di fornire informazioni aggiornate sullo stato di avanzamento dei medicinali biosimilari nell'Unione Europea. La prima edizione di questa breve guida è stata pubblicata nel 2007. Al momento della prima pubblicazione, soli 5 medicinali biosimilari erano stati approvati in Europa, e sia la legislazione che l'esperienza e la... more...
- iSmithers Rapra Publishing 2011; US$ 130.00
The preferred route for drug delivery remains the oral route, but oral drug delivery has now developed beyond traditional dosage forms such as tablets and capsules. Nowadays it is possible to use polymers to allow drugs to be targeted to specific sites in the gastrointestinal tract, and to extend the drug release profile. In addition, polymers can... more...
- 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...