Usp38-Nf33
| Author | : United States Pharmacopeial Convention |
| Publisher | : |
| Total Pages | : |
| Release | : 2014-11-01 |
| Genre | : Medicine |
| ISBN | : 9781936424320 |
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Usp38 Nf33 PDF Download
Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download Usp38 Nf33 PDF full book. Access full book title Usp38 Nf33.
USP 38 - NF 33 The United States Pharmacopeia and National Formulary 2015
| Author | : |
| Publisher | : |
| Total Pages | : 3000 |
| Release | : 2014 |
| Genre | : |
| ISBN | : 9783769263152 |
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Nonclinical Statistics for Pharmaceutical and Biotechnology Industries
| Author | : Lanju Zhang |
| Publisher | : Springer |
| Total Pages | : 705 |
| Release | : 2016-01-13 |
| Genre | : Medical |
| ISBN | : 3319235583 |
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This book serves as a reference text for regulatory, industry and academic statisticians and also a handy manual for entry level Statisticians. Additionally it aims to stimulate academic interest in the field of Nonclinical Statistics and promote this as an important discipline in its own right. This text brings together for the first time in a single volume a comprehensive survey of methods important to the nonclinical science areas within the pharmaceutical and biotechnology industries. Specifically the Discovery and Translational sciences, the Safety/Toxiology sciences, and the Chemistry, Manufacturing and Controls sciences. Drug discovery and development is a long and costly process. Most decisions in the drug development process are made with incomplete information. The data is rife with uncertainties and hence risky by nature. This is therefore the purview of Statistics. As such, this book aims to introduce readers to important statistical thinking and its application in these nonclinical areas. The chapters provide as appropriate, a scientific background to the topic, relevant regulatory guidance, current statistical practice, and further research directions.
Solid State Development and Processing of Pharmaceutical Molecules
| Author | : Michael Gruss |
| Publisher | : John Wiley & Sons |
| Total Pages | : 576 |
| Release | : 2021-09-14 |
| Genre | : Science |
| ISBN | : 3527823069 |
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Solid State Development and Processing of Pharmaceutical Molecules A guide to the lastest industry principles for optimizing the production of solid state active pharmaceutical ingredients Solid State Development and Processing of Pharmaceutical Molecules is an authoritative guide that covers the entire pharmaceutical value chain. The authors—noted experts on the topic—examine the importance of the solid state form of chemical and biological drugs and review the development, production, quality control, formulation, and stability of medicines. The book explores the most recent trends in the digitization and automation of the pharmaceutical production processes that reflect the need for consistent high quality. It also includes information on relevant regulatory and intellectual property considerations. This resource is aimed at professionals in the pharmaceutical industry and offers an in-depth examination of the commercially relevant issues facing developers, producers and distributors of drug substances. This important book: Provides a guide for the effective development of solid drug forms Compares different characterization methods for solid state APIs Offers a resource for understanding efficient production methods for solid state forms of chemical and biological drugs Includes information on automation, process control, and machine learning as an integral part of the development and production workflows Covers in detail the regulatory and quality control aspects of drug development Written for medicinal chemists, pharmaceutical industry professionals, pharma engineers, solid state chemists, chemical engineers, Solid State Development and Processing of Pharmaceutical Molecules reviews information on the solid state of active pharmaceutical ingredients for their efficient development and production.
Applications in Food Sciences
| Author | : Atta-ur-Rahman |
| Publisher | : Bentham Science Publishers |
| Total Pages | : 304 |
| Release | : 2016-04-12 |
| Genre | : Science |
| ISBN | : 1681081431 |
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Applications of NMR Spectroscopy is a book series devoted to publishing the latest advances in the applications of nuclear magnetic resonance (NMR) spectroscopy in various fields of organic chemistry, biochemistry, health and agriculture. The fourth volume of the series features several reviews focusing on NMR spectroscopic techniques in food sciences. Readers will find references on methods used to test food quality, food color analysis, the role of Tannins in wine taste as well as NMR studies on lipid oxidation and large protein complexes.
Good Manufacturing Practices for Pharmaceuticals, Seventh Edition
| Author | : Graham P. Bunn |
| Publisher | : CRC Press |
| Total Pages | : 369 |
| Release | : 2019-02-04 |
| Genre | : Medical |
| ISBN | : 1351646990 |
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This book provides insight into the world of pharmaceutical quality systems and the key elements that must be in place to change the business and organizational dynamics from task-oriented procedure-based cultures to truly integrated quality business systems that are self-detecting and correcting. Chapter flow has been changed to adopt a quality systems organization approach, and supporting chapters have been updated based on current hot topics including the impact of the worldwide supply chain complexity and current regulatory trends.
Advanced Functional Materials
| Author | : Nevin Tasaltin |
| Publisher | : BoD – Books on Demand |
| Total Pages | : 327 |
| Release | : 2020-11-26 |
| Genre | : Technology & Engineering |
| ISBN | : 1839624795 |
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This book was written by authors in the field of preparation of advanced functional materials and their wide-ranging applications. The topics in the book include: preparation of several advanced functional materials, and their applications in sensors, health, concrete, textile, glasses, and pharmacy. In this book, the authors focused on recent studies, applications, and new technological developments in fundamental properties of advanced functional materials.
Profiles of Drug Substances, Excipients and Related Methodology
| Author | : |
| Publisher | : Academic Press |
| Total Pages | : 455 |
| Release | : 2016-02-26 |
| Genre | : Medical |
| ISBN | : 0128051760 |
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Volumes in this widely revered series present comprehensive reviews of drug substances and additional materials, with critical review chapters that summarize information related to the characterization of drug substances and excipients. This organizational structure meets the needs of the pharmaceutical community and allows for the development of a timely vehicle for publishing review materials on this topic. The scope of the Profiles series encompasses review articles and database compilations that fall within one of the following six broad categories: Physical profiles of drug substances and excipients; Analytical profiles of drug substances and excipients; Drug metabolism and pharmacokinetic profiles of drug substances and excipients; Methodology related to the characterization of drug substances and excipients; Methods of chemical synthesis; and Reviews of the uses and applications for individual drug substances, classes of drug substances, or excipients. Contributions from leading authorities Informs and updates on all the latest developments in the field
Pharmaceutical Dosage Forms
| Author | : Larry L. Augsburger |
| Publisher | : CRC Press |
| Total Pages | : 436 |
| Release | : 2017-10-30 |
| Genre | : Medical |
| ISBN | : 1841849774 |
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Pharmaceutical Dosage Forms: Capsules covers the development, composition, and manufacture of capsules. Despite the important role that capsules play in drug delivery and product development, few comprehensive texts on the science and technology of capsules have been available for the research and academic environments. This text addresses this gap, discussing how capsules provide unique capabilities and options for dosage form design and formulation.
Measuring Elemental Impurities in Pharmaceuticals
| Author | : Robert Thomas |
| Publisher | : CRC Press |
| Total Pages | : 483 |
| Release | : 2018-01-29 |
| Genre | : Medical |
| ISBN | : 135198439X |
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Recent regulations on heavy metal testing have required the pharmaceutical industry to monitor a suite of elemental impurities in pharmaceutical raw materials, drug products and dietary supplements. These new directives s are described in the new United States Pharmacopeia (USP) Chapters , , and , together with Q3D, Step 4 guidelines for elemental impurities, drafted by the ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use), a consortium of global pharmaceutical associations, including the European Pharmacopeia (Ph.Eur.), the Japanese Pharmacopeia (JP) and the USP. This book provides a complete guide to the analytical methodology, instrumental techniques and sample preparation procedures used for measuring elemental impurities in pharmaceutical and nutraceutical materials. It offers readers the tools to better understand plasma spectrochemistry to optimize detection capability for the full suite of elemental PDE (Permitted Daily Exposure) levels in the various drug delivery categories. Other relevant information covered in the book includes: The complete guide to measuring elemental impurities in pharmaceutical and nutraceutical materials. Covers heavy metals testing in the pharmaceutical industry from an historical perspective. Gives an overview of current USP Chapters and and ICH Q3D Step 4 Guidelines. Explains the purpose of validation protocols used in Chapter , including how J-values are calculated Describes fundamental principles and practical capabilities of ICP-MS and ICP-OES. Offers guidelines about the optimum strategy for risk assessment Provides tips on how best to prepare and present your data for regulatory inspection. An indispensable resource, the fundamental principles and practical benefits of ICP-OES and ICP-MS are covered in a reader-friendly format that a novice, who is carrying out elemental impurities testing in the pharmaceutical and nutraceutical communities, will find easy to understand.
