How to Optimize Fluid Bed Processing Technology: Part of the Expertise in Pharmaceutical Process Technology Series addresses the important components of fluid bed granulation, providing answers to problems that commonly arise and using numerous practical examples and case studies as reference. This book covers the theoretical concepts involved in fluidization, also providing a description of the choice and functionality of equipment. Additional chapters feature key aspects of the technology, including formulation requirements, process variables, process scale-up, troubleshooting, new development, safety, and process evaluation.

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Developing Solid Oral Dosage Forms: Pharmaceutical Theory and Practice, Second Edition illustrates how to develop high-quality, safe, and effective pharmaceutical products by discussing the latest techniques, tools, and scientific advances in preformulation investigation, formulation, process design, characterization, scale-up, and production operations. This book covers the essential principles of physical pharmacy, biopharmaceutics, and industrial pharmacy, and their application to the research and development process of oral dosage forms. Chapters have been added, combined, deleted, and completely revised as necessary to produce a comprehensive, well-organized, valuable reference for industry professionals and academics engaged in all aspects of the development process.

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Dieses Buch gibt einen fundierten Einstieg in die Grundlagen und neuesten Trends beim Coating pharmazeutischer Produkte. Es richtet sich an Studierende der Pharmatechnik und der Pharmazie ebenso wie an den Praktiker, der an einer schnellen und gründlichen Einführung in die Thematik interessiert ist oder einen Überblick über neueste Entwicklungen im Bereich Coatingtechnik und Coatingmaterialien benötigt.

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Enhancing awareness to increase the development of excipients, this source

provides guidelines for testing new excipients - offers information to ensure that the product ingredients are in compliance with regulatory and quality requirements, and to guarantee the manufacturing and supply chain is in control

includes excipient harmonization activities -  features descriptions on the development and ways of optimal utilization of excipients for the pharmaceutical and biotechnology industries - presents multiple case studies for numerous 

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Uniquely, the Handbook of Pharmaceutical Excipients collects together the essential data on the physical properties of excipients, drug safety and potential drug toxicity. Information is presented in a structured and easy-to-use format.

Written concisely by leading international experts, the Handbook has become the best first drug reference point for users of excipients across many industries.

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Handbook of Cosmeceutical Excipients summarises the current evidence relating to the side effects of cosmeceuticals and highlights the important information that practitioners and consumers need to know.

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Previously published as Hard Capsules, this updated and expanded second edition covers all aspects of capsule technology, including history, standards, methods and equipment used in manufacture, filling, printing, weighing, cleaning and inspecting of both hard and soft capsules.

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This book provides an overview of excipients, their functionalities in pharmaceutical dosage forms, regulation, and selection for pharmaceutical products formulation. It includes development, characterization methodology, applications, and up-to-date advances through the perspectives of excipients developers, users, and regulatory experts.

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The book describes the properties, analytical methods and the applications of different polyvinylpyrrolidone excipients (povidone, crospovidone, copovidone etc.) for use in pharmaceutical preparations. This group of excipients is one of the most important excipients used in modern technology to produce drugs. The book is intended for all persons working in the research, development and quality control of drugs. It gives a survey of all applications in solid, liquid and semisolid dosage forms including many drug formulation examples and more than 600 references to the literature.

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Although the official compendia define a drug substance as to identity, purity, strength, and quality, they normally do not provide other physical or chemical data, nor do they list methods of synthesis or pathways of physical or biological degradation and metabolism. Such information is scattered throughout the scientific literature and the files of pharmaceutical laboratories. Analytical Profiles of Drug Substances and Excipients, brings the latest information together in one source.

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This comprehensive resource covers the fundamentals, formulation, and biopharmaceutical issues of lipid-based drug delivery. It presents the principles of lipid absorption and covers formulation issues, such as dissolution testing and stability testing, and physiological and biopharmaceutical issues, including the role of specific enzymes, the evaluation of transport systems in the body, and the mechanisms governing the transport of water-insoluble drugs.

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