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- 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...
- 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...
- Pharma Book Syndicate 2008; US$ 50.00
Dispensing of medication remains an art and a most exacting science, which pharmacists are supposed to master. Obviously modern pharmacists have to cope with their changing role and this has been the focal theme in presenting this text on Modern Dispensing Pharmacy. Attempt has been made to inculcate the newer concepts and latest knowledge relevant... more...
- Duncker & Humblot 2008; US$ 74.48
Hauptbeschreibung Der Bereich der Arzneimittelwerbung erfährt in Deutschland und in Europa eine starke Regulierung. Die Einschränkungen der Arzneimittelwerbung durch nationale und europäische Vorschriften basieren vorrangig auf der Einstufung von Arzneimitteln als besonders gefährliche Verbrauchsgüter, somit vorrangig auf Erwägungen des Gesundheitsschutzes.... more...
- Wiley 2014; US$ 125.00
Polymers have played a critical role in the rational design and application of drug delivery systems that increase the efficacy and reduce the toxicity of new and conventional therapeutics. Beginning with an introduction to the fundamentals of drug delivery, Engineering Polymer Systems for Improved Drug Delivery explores traditional drug delivery... more...
- Taylor and Francis 2014; US$ 99.95
Notoriously cumbersome to isolate and challenging to synthesize, the path of natural products to viable drugs is an arduous journey. Yet compounds isolated from nature have long been known to possess fascinating structures, biological profiles and pharmaceutical potential far greater than anything made by man. Natural Products Chemistry: Sources,... 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$ 49.24
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...
- Elsevier Science 1991; US$ 72.95
Biotechnological Innovations in Health Care provides insight and information on how modern biotechnology may be applied to produce useful medicinal products. This book begins with a general introduction to biotechnology, summarizing its historical development, possible role in health care, and impact on society. The stages involved in developing... more...
- Taylor and Francis 2014; US$ 159.95
A great deal of confusion and uncertainty over genotoxic impurity (GTI) identification, assessment, and control exists in the pharmaceutical industry today. Pharmaceutical Industry Practices on Genotoxic Impurities strives to facilitate scientific and systematic consensus on GTI management by presenting rationales, strategies, methods, interpretations,... more...
- Learning Express, LLC 2014; US$ 9.99
This handy eBook guide helps users master more than 600 of the most-tested terms and concepts on the PTCE and ExCPT tests, so users can score well on these certification exams and achieve their goals of becoming pharmacy technicians. more...