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, pharmacological and toxicological characteristics - when they are a component of pharmaceutical products and formulations. The book discusses in detail;
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;particle interaction;manufacturing processes;quality by design;and a general discussion of the industry. Pharmaceutical Powder and Particles;
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pharmaceutical products, including currently approved products and innovative products such as small proteins, instantly liquifiable powders, and;
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Nanoparticles, products of nanotechnology, are of increasing interest to the pharmaceutical community. They can increase drug solubility;
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Design and Manufacturing of Plastics Products: Integrating Conventional Methods and Innovative Technologies brings together detailed;
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(API's) and 2) Drug Product Design, Development and Modeling. The active pharmaceutical ingredients book puts the focus on the chemistry;
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design and pharmaceutical production processes design/synthesis; modeling and simulation of the pharmaceutical processing unit operation;
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and behavior, there has been no text that explores the power of particulate science in the design, manufacture, and control of quality;
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This book is a structured approach to designing a product and its associated manufacturing process. It shows pharmaceutical engineers and;
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. Written by a top biostatistics researcher, Biosimilars: Design and Analysis of Follow-on Biologics is the first book entirely devoted to the;
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. Written by a top biostatistics researcher, Biosimilars: Design and Analysis of Follow-on Biologics is the first book entirely devoted to the;
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for specialists and researchers in pharmaceutical drug development, regulation, manufacturing, and others in the pharmaceutical sciences.;
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Sterile Pharmaceutical Products: Process Engineering Applications addresses the key concepts and applications of the sterile pharmaceutical;
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In 2002, the U.S. Food and Drug Administration (FDA) launched the Pharmaceutical Quality for the 21st Century Initiative to encourage;
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/>The book is essential reading for specialists and researchers in pharmaceutical drug development, regulation, manufacturing, and others in the;
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regulation of all pharmaceutical delivery systems including transdermal and topical products have been happening on a continuous basis. In light;
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regulation of all pharmaceutical delivery systems including transdermal and topical products have been happening on a continuous basis. In light;
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This authoritative guide will serve as the most current source on the design and manufacturing of parenteral dispersed systems-showcasing;
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, process analytical technology and quality-by-design * Contains contributions from researchers in leading pharmaceutical companies, the FDA, and;
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advanced specialist topics that can be systematically applied to industry Pharmaceutical Quality by Design offers a guide to the principles and;
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nanoparticles and smart, thermally responsive particles. They also cover surface tailoring of various organic and inorganic nanoparticles by polymers;
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This authoritative guide will serve as the most current source on the design and manufacturing of parenteral dispersed systems-showcasing;
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Pharmaceutical manufacturers are constantly facing quality crises of drug products, leading to an escalating number of product recalls and;
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Nanoparticles are a result of rapid scientific progress. Nanoparticles refer to particles that are sized between 1-100 nm in at least one;
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Monodispersed Particles, Second Edition, covers all aspects of monodispersed particles, including inorganic and polymer particles and their;
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Design and Development of New Nanocarriers focuses on the design and development of new nanocarriers used in pharmaceutical applications;
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European Good Manufacturing Practice guidelines, Good Pharmaceutical Manufacturing Practice: Rationale and Compliance gleans the most important;
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