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- 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...
Rift-lines within european regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into accountDiplomica Verlag 2014; US$ 39.75
Biopharmaceutical medicinal products (biologics) represent a huge financial market. Thus upon patent protection expiry of the innovator (reference) biologic there is interest from industry to gain a portion of this market by launching a 'similar' biologic at a reduced development cost, thus boosting potential gains. The EMA responded to this desire... 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...
- Pharma Book Syndicate 2006; US$ 50.00
This book has made an attempt to present the physical pharmacy experiments covering almost full requirements of various universities in a simple and understandable manner. Though it has been accepted to use only SI units in all scientific disciplines, pharmacy not being an exception, we are yet to completely transform to the new system of units. The... more...
- Studium Press 2010; US$ 110.00
Herbal drugs have a prolonged history of frequent use and documentation in texts of established systems of medicine indigenous to a particular country. There is a great demand for these medicines in the developed as well as developing countries because of their wide biological activities, higher safety margin than the synthetic drugs and lesser costs.... more...
- Studium Press 2010; US$ 110.00
Nature has been providing products that have implications as pharmacological agents. There is even a traditional belief that all the plants grown on this planet have some or other therapeutic/physiological attributes. Natural products isolated in original form are often not fit for their use in human or animal medicine. Sometimes they don?t have the... more...
- Pharmaceutical Press 2010; US$ 93.73
The second edition of this practical guide to the safe administration of medicines via enteral feeding tubes has been revised and updated to include 40 new monographs adding to the comprehensive collection. Ten chapters provide the background knowledge to inform clinical decisions, including information on: types of enteral feeding tubes, syringes... 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...