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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...
- Future Medicine Ltd 2012; US$ 260.00
Emulsions are the next most widely used adjuvants in human vaccines after alum-based formulations. Their importance in modern vaccines is underscored by their demonstrated record of stability, safety, and enabling of antigen dose-sparing. more...
- Wiley 2013; US$ 159.95 US$ 138.62
Biotechnology and Biopharmaceuticals: Transforming Proteins and Genes into Drugs, Second Edition addresses the pivotal issues relating to translational science, including preclinical and clinical drug development, regulatory science, pharmaco-economics and cost-effectiveness considerations. The new edition also provides an update on new proteins... more...
- CRC Press 2008; US$ 45.95
Get Through MRCP Part 1: BOFs provides over 600 questions and answers, allowing the reader to test their knowledge in preparation for the MRCP Part 1 examination. Questions are presented in the style used in the real examination, and answers are supplemented with useful additional explanatory material to help the reader understand why their answer... more...
- Elsevier Science 2013; 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 and... more...
- Wiley 2014; US$ 212.00 US$ 183.73
This second edition of a global bestseller has been completely redesigned and extensively rewritten to take into account the new Quality by Design (QbD) and lifecycle concepts in pharmaceutical manufacturing. As in the first edition, the fundamental requirements for analytical method validation are covered, but the second edition describes how these... more...
- Taylor and Francis 2015; US$ 43.95
In recent years medicalization, the process of making something medical, has gained considerable ground and a position in everyday discourse. In this multidisciplinary collection of original essays, the authors expertly consider how issues around medicalization have developed, ways in which it is changing, and the potential shapes it will take in... more...
- Pharmaceutical Press 2015; US$ 46.00
This book covers the technical, practical and legal aspects that you should consider before prescribing or administering drugs via enteral feeding tubes. more...