Wiley, 2012. - 886 p. - Cost-effective manufacturing of biopharmaceutical products is rapidly gaining in importance, while healthcare systems across the globe are looking to contain costs and improve efficiency. To adapt to these changes, industries need to review and streamline their manufacturing processes. This two volume handbook systematically addresses the key steps and challenges in the production process and provides valuable information for medium to large scale producers of biopharmaceuticals. It is divided into seven major parts: - Upstream Technologies - Protein Recovery - Advances in Process Development - Analytical Technologies - Quality Control - Process Design and Management - Changing Face of Processing With contributions by around 40 experts from academia as well as small and large biopharmaceutical companies, this unique handbook is full of first-hand knowledge on how to produce biopharmaceuticals in a cost-effective and quality-controlled manner.
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The 10th ed. — Philadelphia-Baltimore-NY: Wolters Kluwer, 2014. — 794 p. The purpose of this text is to introduce pharmacy students to the principles, practices, and technologies applied in the preparation of pharmaceutical dosage forms and drug delivery systems. An integrated presentation is used in this textbook to demonstrate the interrelationships between pharmaceutical and...
1 edition. — Wiley-Interscience, 2008. — 1384 p. — ISBN: 978-0-470-25958-0. This Handbook of Manufacturing Techniques focuses on a new aspect of the drug development challenge: producing and administering the physical drug products that we hope are going to provide valuable new pharmacotherapeutic tools in medicine. These 34 chapters cover the full range of approaches to...
Wiley-Interscience, 2008. — 856 p. — ISBN: 978-0-470-25959-7. This Handbook of Manufacturing: Regulations and Quality focuses on all regulatory aspects and requirements that govern how drugs are produced for evaluation (and later, sale to and use in) humans. The coverage ranges from what the issues are at the early stages (when the amounts are small and the materials of limited...
Wiley-Interscience, John Wiley & Sons, Inc., 2007. — 1659 p. — ISBN: 978-0-471-21386-4. This Handbook of Pharmaceutical Biotechnology represents a unique attempt to overview the full range of approaches to discovering, selecting, and producing potentially new therapeutic moieties resulting from biological process. Such moieties are the backbone of both the pharmaceutical...
Wiley, 2002. - 313 p. This volume focuses on pharmaceutical biotechnology as a key area of life sciences. The complete range of concepts, processes and technologies of biotechnology is applied in modern industrial pharmaceutical research, development and production. The results of genome sequencing and studies of biological-genetic function are combined with chemical,...
Monograph, Oxford Cambridge UK, Woodhead Publishing Limited, 2013. - 370 p. Failure to adequately control any microbial challenge associated within process or product by robust sterilisation will result in a contaminated marketed product, with potential harm to the patient. Sterilisation is therefore of great importance to healthcare and the manufacturers of medical devices and...