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Handbook Of Modern Pharmaceutical Analysis

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Handbook of Modern Pharmaceutical Analysis

Handbook of Modern Pharmaceutical Analysis Book
Author : Satinder Ahuja,Stephen Scypinski
Publisher : Academic Press
Release : 2001
ISBN : 9780120455553
Language : En, Es, Fr & De

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Book Description :

This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories. No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.

Handbook of Modern Pharmaceutical Analysis

Handbook of Modern Pharmaceutical Analysis Book
Author : Satinder Ahuja,Stephen Scypinski
Publisher : Academic Press
Release : 2010-11-11
ISBN : 9780123759818
Language : En, Es, Fr & De

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Book Description :

Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations Features detailed coverage of QA, ethics, and regulatory guidance (quality by design, good manufacturing practice), as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS

Handbook of Modern Pharmaceutical Analysis

Handbook of Modern Pharmaceutical Analysis Book
Author : Satinder Ahuja,Stephen Scypinski
Publisher : Elsevier
Release : 2001-08-02
ISBN : 9780080488929
Language : En, Es, Fr & De

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Book Description :

This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories. No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.

Handbook of Isolation and Characterization of Impurities in Pharmaceuticals

Handbook of Isolation and Characterization of Impurities in Pharmaceuticals Book
Author : Satinder Ahuja,Karen Mills Alsante
Publisher : Academic Press
Release : 2003-08
ISBN : 9780120449828
Language : En, Es, Fr & De

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Book Description :

The United States Food and Drug Administration (FDA) and other regulatory bodies around the world require that impurities in drug substance and drug product levels recommended by the International Conference on Harmonisation (ICH) be isolated and characterized. Identifying process-related impurities and degradation products also helps us to understand the production of impurities and assists in defining degradation mechanisms. When this process is performed at an early stage, there is ample time to address various aspects of drug development to prevent or control the production of impurities and degradation products well before the regulatory filing and thus assure production of a high-quality drug product. This book, therefore, has been designed to meet the need for a reference text on the complex process of isolation and characterization of process-related (synthesis and formulation) impurities and degradation products to meet critical requlatory requirements. It's objective is to provide guidance on isolating and characterizing impurities of pharmaceuticals such as drug candidates, drug substances, and drug products. The book outlines impurity identification processes and will be a key resource document for impurity analysis, isolation/synthesis, and characterization. - Provides valuable information on isolation and characterization of impurities. - Gives a regulatory perspective on the subject. - Describes various considerations involved in meeting regulatory requirements. - Discusses various sources of impurities and degredation products.

Pharmaceutical Principles of Solid Dosage Forms

Pharmaceutical Principles of Solid Dosage Forms Book
Author : Jens T. Carstensen
Publisher : CRC Press
Release : 1993-08-16
ISBN : 9780877629559
Language : En, Es, Fr & De

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Book Description :

This comprehensive guide presents the principles underlying the formation, properties and manufacturing of solid dosage forms. Developed by a leading pharmaceutical expert with 25 years of experience, this book is a precise handbook to powder dosage forms, hard shell capsules, milling, tablet, granulation and drying, stability, crystalline solids, DSC and amorphates, hygroscopicity, packaging, micromeritics, sustained release, and more. Designed for use by development pharmacists, analytical chemists, production pharmacists, and pharmacy professors and students, this book emphasizes U.S. validation principles; the interrelationship between formulation, manufacturing and existing USP and FDA guidelines; and aspects of pharmaceutics important to IND and NDA submission and subsequent supplements.

Remington

Remington Book
Author : David B. Troy,Paul Beringer
Publisher : Lippincott Williams & Wilkins
Release : 2006
ISBN : 9780781746731
Language : En, Es, Fr & De

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Book Description :

For over 100 years, Remington has been the definitive textbook and reference on the science and practice of pharmacy. This Twenty-First Edition keeps pace with recent changes in the pharmacy curriculum and professional pharmacy practice. More than 95 new contributors and 5 new section editors provide fresh perspectives on the field. New chapters include pharmacogenomics, application of ethical principles to practice dilemmas, technology and automation, professional communication, medication errors, re-engineering pharmacy practice, management of special risk medicines, specialization in pharmacy practice, disease state management, emergency patient care, and wound care. Purchasers of this textbook are entitled to a new, fully indexed Bonus CD-ROM, affording instant access to the full content of Remington in a convenient and portable format.

Pharmaceutical Stress Testing

Pharmaceutical Stress Testing Book
Author : Steven W. Baertschi,Karen M. Alsante,Robert A. Reed
Publisher : CRC Press
Release : 2016-04-19
ISBN : 1439801800
Language : En, Es, Fr & De

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Book Description :

The second edition of Pharmaceutical Stress Testing: Predicting Drug Degradation provides a practical and scientific guide to designing, executing and interpreting stress testing studies for drug substance and drug product. This is the only guide available to tackle this subject in-depth. The Second Edition expands coverage from chemical stability into the physical aspects of stress testing, and incorporates the concept of Quality by Design into the stress testing construct / framework. It has been revised and expanded to include chapters on large molecules, such as proteins and antibodies, and it outlines the changes in stress testing that have emerged in recent years. Key features include: A renowned Editorial team and contributions from all major drug companies, reflecting a wealth of experience. 10 new chapters, including Stress Testing and its relationship to the assessment of potential genotoxic degradants, combination drug therapies, proteins, oligonucleotides, physical changes and alternative dosage forms such as liposomal formulations Updated methodologies for predicting drug stability and degradation pathways Best practice models to follow An expanded Frequently Asked Questions section This is an essential reference book for Pharmaceutical Scientists and those working in Quality Assurance and Drug Development (analytical sciences, formulations, chemical process, project management).

Modern Methods of Particle Size Analysis

Modern Methods of Particle Size Analysis Book
Author : Howard G. Barth
Publisher : John Wiley & Sons
Release : 1984-09-11
ISBN : 9780471875710
Language : En, Es, Fr & De

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Book Description :

Specialists in the field discuss the latest developments in particle size analysis, presenting an overview of state-of-the-art methodologies and data interpretation. Topics include commercial instrumentation, photon correlation spectroscopy, Fraunhofer Diffraction, field-flow fractionation, and detection systems for particle chromatography.

Handbook of Powder Science and Technology

Handbook of Powder Science and Technology Book
Author : Mohammed E. Fayed,Lambert Otten
Publisher : Springer
Release : 1984-05-30
ISBN : 0987650XXX
Language : En, Es, Fr & De

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Book Description :

Now in its second edition, this authoritative reference provides comprehensive coverage of the fundamentals of powder science and technology and builds upon them.

The Law of Chemical and Pharmaceutical Invention

The Law of Chemical and Pharmaceutical Invention Book
Author : Jerome Rosenstock
Publisher : Aspen Publishers Online
Release : 1999
ISBN : 0735502641
Language : En, Es, Fr & De

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Book Description :

Protecting new inventions requires legal acuity and technical expertise. The Law of Chemical and Pharmaceutical Invention combines insightful analysis of the relevant intellectual property law with practical advice on how best to protect your clients' interests, providing the nuts and bolts of both patent and non-patent approaches. You'll find incisive and practical expert guidance on: Eligibility -- Genetic engineering -- Biotechnological patents -- Novelty -- Obviousness -- Patent review -- Patent term extensions -- Enforcement of patent rights -- Infringement defenses. -- Appeals practice -- Ownership and transfer of invention rights -- Patent termination. The book also includes sample diagrams of chemical structures, sample filing forms, claim formats, sample design formats and trademarks, and other convenient practice materials.

Handbook of Forensic Drug Analysis

Handbook of Forensic Drug Analysis Book
Author : Fred Smith
Publisher : Elsevier
Release : 2004-12-31
ISBN : 9780080472898
Language : En, Es, Fr & De

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Book Description :

The Handbook of Forensic Drug Analysis is a comprehensive chemical and analytic reference for the forensic analysis of illicit drugs. With chapters written by leading researchers in the field, the book provides in-depth, up-to-date methods and results of forensic drug analyses. This Handbook discusses various forms of the drug as well as the origin and nature of samples. It explains how to perform various tests, the use of best practices, and the analysis of results. Numerous forensic and chemical analytic techniques are covered including immunoassay, gas chromatography, and mass spectrometry. Topics range from the use of immunoassay technologies for drugs-of-abuse testing, to methods of forensic analysis for cannabis, hallucinogens, cocaine, opioids, and amphetamine. The book also looks at synthetic methods and law enforcement concerns regarding the manufacture of illicit drugs, with an emphasis on clandestine methamphetamine production. This Handbook should serve as a widely used reference for forensic scientists, toxicologists, pharmacologists, drug companies, and professionals working in toxicology testing labs, libraries, and poison control centers. It may also be used by chemists, physicians and those in legal and regulatory professions, and students of graduate courses in forensic science. Contributed to by leading scientists from around the world The only analysis book dedicated to illicit drugs of abuse Comprehensive coverage of sampling methods and various forms of analysis

Purity Determinations by Thermal Methods

Purity Determinations by Thermal Methods Book
Author : Roger L. Blaine,Clifford K. Schoff
Publisher : ASTM International
Release : 1984-04
ISBN : 9780803102224
Language : En, Es, Fr & De

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Book Description :

Download Purity Determinations by Thermal Methods book written by Roger L. Blaine,Clifford K. Schoff, available in PDF, EPUB, and Kindle, or read full book online anywhere and anytime. Compatible with any devices.

Sigma Aldrich Labware

Sigma  Aldrich Labware Book
Author : Anonim
Publisher : Unknown
Release : 2020-12-03
ISBN : 0987650XXX
Language : En, Es, Fr & De

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Book Description :

Download Sigma Aldrich Labware book written by , available in PDF, EPUB, and Kindle, or read full book online anywhere and anytime. Compatible with any devices.

Book Review Index

Book Review Index Book
Author : Gale Group
Publisher : Book Review Index Cumulation
Release : 2003-08
ISBN : 9780787665791
Language : En, Es, Fr & De

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Book Description :

'Book Review Index' provides quick access to reviews of books, periodicals, books on tape and electronic media representing a wide range of popular, academic and professional interests. More than 600 publications are indexed, including journals and national general interest publications and newspapers. 'Book Review Index' is available in a three-issue subscription covering the current year or as an annual cumulation covering the past year.

Drugs Pharmaceutical Technology Handbook

Drugs   Pharmaceutical Technology Handbook Book
Author : NIIR Board
Publisher : ASIA PACIFIC BUSINESS PRESS Inc.
Release : 2004-01-01
ISBN : 8178330547
Language : En, Es, Fr & De

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Book Description :

Drugs and pharmaceutical industry plays a vital role in the economic development of a nation. It is one of the largest and most advanced sectors in the world, acting as a source for various drugs, medicines and their intermediates as well as other pharmaceutical formulations. India has come a long way in this field, from a country importing more than 95% of its requirement of drugs and pharmaceuticals; India now is exporting it even to developed countries. Being the intense knowledge driven industry, it offers innumerable business opportunities for the investors/ corporate the world over. The existence of well defined and strong pharmaceutical industry is important for promoting and sustaining research and developmental efforts and initiatives in an economy as well as making available the quality medicines to all at affordable prices. That is, it is essential to improve the health status of the individuals as well as the society as a whole, so that positive contributions could be made to the economic growth and regional development of a country. On the global platform, India holds fourth position in terms of volume and thirteenth position in terms of value of production in pharmaceuticals. The pharmaceutical industry has been producing bulk drugs belonging to all major therapeutic groups requiring complicated manufacturing processes as well as a wide range of pharmaceutical machinery and equipments. The modern Indian Pharmaceutical Industry is recent and its foundation was laid in the beginning of the current century. The pharmaceutical industry can be broadly categorised as bulk drugs, formulations, IV fluids and pharmaceutical aids (such as medical equipment, hospital disposables, capsules, etc.). Special feature of the pharmaceutical industry is a large number of manufacturers in the small scale sector. The government is also encouraging the SSI sector providing some incentives. The recent developments in the technology and R & D work in this field have led to the increased growth rate of industries and have established Indian Pharmaceutical industries in the international market. The content of the book includes information about properties, general methods of analysis, methods of manufacture, of different types of drugs and pharmaceuticals. Some of the fundamentals of the book are polymeric materials used in drug delivery systems , theoretical aspects of friction and lubrication , a convenient method for conversion of quinine to quinidine, formulation and evaluation of bio-available enteric-coated erythromycin and metronidazole tablets, extraction of virginiamycin, antipyretics and analgesics, column chromatographic assay of aspirin tablets, differentiating titration of phenacetin and caffeine, infrared spectra of some compounds of pharmaceutical interest etc. This book covers an intensive study on manufacturing, production, formulation and quality control of drugs and pharmaceuticals with technology involved in it. This book is an invaluable resource for technologists, professionals and those who want to venture in this field.

Handbook of Analytical Therapeutic Drug Monitoring and Toxicology 1996

Handbook of Analytical Therapeutic Drug Monitoring and Toxicology  1996  Book
Author : Steven H.Y. Wong,Irving Sunshine
Publisher : CRC Press
Release : 2017-11-22
ISBN : 1351364278
Language : En, Es, Fr & De

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Book Description :

Adapting modern advances in analytical techniques to daily laboratory practices challenges many toxicologists, clinical laboratories, and pharmaceutical scientists. The Handbook of Analytical Therapeutic Drug Monitoring and Toxicology helps you keep abreast of the innovative changes that can make your laboratory - and the studies undertaken in it - a success. This volume simplifies your search for appropriate techniques, describes recent contributions from leading investigators, and provides valuable evaluations and advice.

Handbook of Analysis of Oligonucleotides and Related Products

Handbook of Analysis of Oligonucleotides and Related Products Book
Author : Jose V. Bonilla,G. Susan Srivatsa
Publisher : CRC Press
Release : 2011-02-23
ISBN : 1439819939
Language : En, Es, Fr & De

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Book Description :

Oligonucleotides represent one of the most significant pharmaceutical breakthroughs in recent years, showing great promise as diagnostic and therapeutic agents for malignant tumors, cardiovascular disease, diabetes, viral infections, and many other degenerative disorders. The Handbook of Analysis of Oligonucleotides and Related Products is an essential reference manual on the practical application of modern and emerging analytical techniques for the analysis of this unique class of compounds. A strong collaboration among thirty leading analytical scientists from around the world, the book provides readers with a comprehensive overview of the most commonly used analytical techniques and their advantages and limitations in assuring the identity, purity, quality, and strength of an oligonucleotide intended for therapeutic use. Topics discussed include: Strategies for enzymatic or chemical degradation of chemically modified oligonucleotides toward mass spectrometric sequencing Purity analysis by chromatographic or electrophoretic methods, including RP-HPLC, AX-HPLC, HILIC, SEC, and CGE Characterization of sequence-related impurities in oligonucleotides by mass spectrometry and chromatography Structure elucidation by spectroscopic methods (IR, NMR, MS) as well as base composition and thermal melt analysis (Tm) Approaches for the accurate determination of molar extinction coefficient of oligonucleotides Accurate determination of assay values Assessment of the overall quality of oligonucleotides, including microbial analysis and determination of residual solvents and heavy metals Strategies for determining the chemical stability of oligonucleotides The use of hybridization techniques for supporting pharmacokinetics and drug metabolism studies in preclinical and clinical development Guidance for the presentation of relevant analytical information towards meeting current regulatory expectations for oligonucleotide therapeutics This resource provides a practical guide for applying state-of-the-art analytical techniques in research, development, and manufacturing settings.

Handbook of Pharmaceutical Wet Granulation

Handbook of Pharmaceutical Wet Granulation Book
Author : Ajit S. Narang,Sherif I.F. Badawy
Publisher : Academic Press
Release : 2018-08-31
ISBN : 0323481035
Language : En, Es, Fr & De

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Book Description :

Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide spectrum of relevant and contemporary wet granulation topics, techniques and processes. The books' focus on process analytical technology, quality by design principles, granulation equipment, modeling, scale-up, control and real time release makes it a timely and valuable resource for all those involved in pharmaceutical wet granulation. Discusses fundamentals of theory and current industrial practice in the field of wet granulation, including product and process design and role of material properties in wet granulation Examines the modern evolution of wet granulation through current topics such as established and novel process analytical technologies (PATs), and product development and scale-up paradigms Written for scientists working within the pharmaceutical industry, as well as academics, regulatory officials and equipment vendors who provide PAT tools and granulation equipment

Chemical Stability of Pharmaceuticals

Chemical Stability of Pharmaceuticals Book
Author : Kenneth A. Connors,Gordon L. Amidon,Valentino J. Stella,Valentino J Stella
Publisher : John Wiley & Sons
Release : 1986-10-13
ISBN : 9780471879558
Language : En, Es, Fr & De

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Book Description :

Provides a sound theoretical basis for understanding chemical kinetics and its uses in studying drug stability. Treats the calculations, approximations, and estimates that are useful to the pharmacist in professional practice, and presents a collection of selected drug-stability data from the pharmaceutical literature. This Handbook makes accessible to the pharmacist much of the information necessary to make pharmaceutical decisions about drug stability. Changes in this edition include thorough revision of the chapter on oxidation, addition of a new chapter on solid-state stability, and a tripling of the number of stability monographs. All monographs figures have been redrawn, most of them from published data, and all sources are cited.

Analytical Instrumentation Handbook

Analytical Instrumentation Handbook Book
Author : Jack Cazes
Publisher : CRC Press
Release : 2004-11-30
ISBN : 9780849390395
Language : En, Es, Fr & De

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Book Description :

Compiled by the editor of Dekker's distinguished Chromatographic Science series, this reader-friendly reference is as a unique and stand-alone guide for anyone requiring clear instruction on the most frequently utilized analytical instrumentation techniques. More than just a catalog of commercially available instruments, the chapters are wri