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Validation of Pharmaceutical Processes
CRC Press 2007; US$ 356.00Completely revised and updated to reflect the significant advances in pharmaceutical production and regulatory expectations, this third edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and competitive. The many chapters added to the prior compilation examine validation... more...
Enhancement in Drug Delivery
CRC Press 2006; US$ 239.95Focusing on research, this book provides a comprehensive review and detailed coverage of all routes of drug administration. It presents both the basics of the route of administration and the methods for enhancing it. It includes a chapter devoted to chemical enhancers that apply to more than one route of administration. more...
Nanotechnology in Drug Delivery
Springer 2008; US$ 109.99The reader will be introduced to various aspects of the fundamentals of nanotechnology based drug delivery systems and the application of these systems for the delivery of small molecules, proteins, peptides, oligonucleotides and genes. How these systems overcome challenges offered by biological barriers to drug absorption and drug targeting will also... more...
Stimuli Responsive Drug Delivery Systems
iSmithers Rapra Publishing 2010; US$ 250.00Stimuli responsive drug delivery systems have emerged as one of the most innovative classes of polymer materials of modern materials science. The polymer architectures exhibiting a large change in their physico chemical behaviors in response to minor signals from the environments have fabricated potentially useful materials for pharmaceutical and biomedical... more...
Biologics in General Medicine
Springer 2007; US$ 159.99Comprises the relevant aspects for the clinical application of biologics. This book describes the "differential therapy" with biologics namely in the fields of dermatology, rheumatology, gastroenterology, and neurology. It is intended for researchers and clinicians. more...
Sources of Contamination in Medicinal Products and Medical Devices
Wiley 2012; US$ 150.00The first one-volume guide to sources of contamination in pharmaceuticals and medical devices Most books dealing with contaminants in medicinal products often focus on analytical methods for detecting nonspecific impurities. Key to the work of the pharmaceutical chemist, this unique reference helps identify the sources of contamination in medicinal... more...
Microbial Limit and Bioburden Tests
Taylor & Francis 2008; US$ 209.95A guide to microbial limit methodologies. It includes chapters that provide coverage of biofilms, environmental monitoring, and microbial identification. It also addresses topics, such as water testing. more...
Isolation Technology
CRC Press 2004; US$ 279.95The most significant changes in isolation technology during the past five years have not been in the technology itself but in its increased acceptance. This acceptance is clearly demonstrated by the series of monographs, guidelines, and standards produced by regulatory bodies to describe best practice in the design and operation of isolators. Thoroughly... more...
Guide to Microbiological Control in Pharmaceuticals and
CRC Press 2005; US$ 189.95A comprehensive review of the practical issues facing the industrial microbiologist of today including the appreciation of the developing role of rapid methods and the accompanying regulatory requirements. more...
Current Trends of Supercritical Fluid Technology in Pharmaceutical, Nutraceutical and Food Processing Industries
Bentham Science Publishers 2010; US$ 59.00Supercritical fluid technology can be seen as a green and environmentally friendly alternative to conventional. Current information on these topics is spread through different publications in different peer-reviewed journals. The editors were therefore of the opinion that this information should be gathered in an Ebook which presents some reviews on... more...
