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Most popular at the top
- Pan Stanford Publishing 2015; US$ 149.95
Recent years have seen the development of novel technologies that use nanoparticles and microparticles to deliver vaccines by the oral and microneedle-based transdermal route of administration. These new technologies enable the formulation of vaccine particles containing vaccine antigens, without loss of their biological activity during the formulation... more...
- World Scientific Publishing Company 2012; US$ 119.00
Nanomaterials, with their unique size-dependent physical and chemical properties, have shown promising advantages as drug and gene delivery vehicles, ultra-sensitive intracellular detectors and novel therapeutic drugs. Nanopharmaceutics is one of the disciplines that will benefit the most from this technology.Nanotechnology will have a revolutionary... more...
- Springer New York 2008; US$ 269.00
This book explores various fundamental aspects of nanotechnology-based drug delivery systems. It also covers the applications of these systems for the delivery of small molecules, proteins, peptides, oligonucleotides and genes. more...
- Elsevier Science 2013; US$ 174.95
Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics is a complete reference devoted to the nonclinical safety assessment of novel biopharmaceuticals, biosimilars, vaccines, cell and gene therapies and blood products. This book compares and contrasts these types of biologics with one another and with small molecule... more...
- Springer Berlin Heidelberg 2008; US$ 99.00
Die pharmazeutische Industrie weist gegenüber normalen Industriebetrieben eine Reihe von Besonderheiten auf, die in der allgemeinen Industriebetriebslehre nicht ausreichend berücksichtigt werden. Die Entwicklung einer eigenständigen Pharmabetriebslehre erscheint daher notwendig. Das vorliegende Buch befasst sich mit den speziellen volkswirtschaftlichen... more...
- CRC Press 2003; US$ 157.95
Written especially for the pharmaceutical industry professional, this book addresses each part of the life-cycle of engineering change control. It covers issues in the EU and US and describes the operational requirements and responsibilities that ensure change controls are effectively applied and recorded. Providing guidance on how to demonstrate that... more...
- Wiley 2008; US$ 232.00
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more... more...
- Wiley 2008; US$ 228.00
With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug... more...
- CRC Press 2007; US$ 157.95
This title demonstrates how designed experiments are the most scientific, efficient, and cost effective method of data collection for validation in a laboratory setting. Intended as a learn-by-example guide, Pharmaceutical and Medical Device Validation by Experimental Design demonstrates why designed experiments are the most logical and rational approach... more...
- Elsevier Science 2002; US$ 310.00
The Pharmaceutical Engineering Series is a comprehensive reference for the pharmaceutical professional covering all aspects from quality, documentation and validation through manufacturing processes to facility design and management. In 'Quality', Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the... more...