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Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Dissolution Testing Devices Automation;
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An expertly written source on the devices, systems, and technologies used in the dissolution testing of oral pharmaceutical dosage forms;
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in dissolution testing, dissolution of suspensions, and drug release of non-oral products. Of particular interest to the industrial pharmaceutical;
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book captures the essence of major pharmaceutical applications (assays, stability testing, impurity testing, dissolution testing, cleaning;
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Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug;
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: Tablets, Volume Three examines: automation in tablet manufacture setting dissolution specifications testing and evaluating tablets;
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, analytical development, formulation development, dissolution testing, manufacturing, stability studies, bioequivalence testing, risk and assessment;
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, some physical parameters, potency, and disintegration and dissolution profile) of Losartan potassium tablets from different pharmaceutical;
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reference book. It describes analytical methodologies like dissolution testing, solid state NMR, Raman microscopy, and LC-MS and presents;
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This book is a research work which is quite unique, knowledgeable and resourceful. Hence, areas of pharmaceutical research that focus on;
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A one-stop resource for researchers, developers, and post graduate students in pharmaceutical science. This handbook and ready reference;
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Pharmaceutical packaging requires a greater knowledge of materials and a greater intensity of testing than most other packed products, not;
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issues in the solid state science and particularly in the pharmaceutical world. In this context, multi-component crystalline materials like co;
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leading statisticians, scientists, and clinicians from the pharmaceutical industry, academia, and regulatory agencies, Multiple Testing Problems;
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dissolution testing and explores current issues and recent developments in stability studies. To ensure the safety of consumers, professionals;
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dissolution testing and explores current issues and recent developments in stability studies. To ensure the safety of consumers, professionals;
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involved in the testing and use of pharmaceuticals on human beings Investigates issues such as whether choice of drug should lie with the;
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Design and Manufacture of Pharmaceutical Tablets offers real world solutions and outcomes of formulation and processing challenges;
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Martin's Physical Pharmacy and Pharmaceutical Sciences is considered the most comprehensive text available on the physical, chemical, and;
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This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and;
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This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and;
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is adopted globally by both individuals and organizations working within pharmaceutical research and development, manufacture, and testing worldwide;
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the principles of lipid absorption and covers formulation issues, such as dissolution testing and stability testing, and physiological and;
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Pharmaceutical Microbiology encompasses those aspects of Microbiology which impact directly upon the development, production and use;
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global experts in dissolution testing In Vitro Drug Release Testing of Special Dosage Forms will find a place on the bookshelves of anyone;
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Recent regulations on heavy metal testing have required the pharmaceutical industry to monitor a suite of elemental impurities;
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Recent regulations on heavy metal testing have required the pharmaceutical industry to monitor a suite of elemental impurities;
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