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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.

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).

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.

Sigma Aldrich Labware

Sigma  Aldrich Labware Book
Author : Anonim
Publisher : Unknown
Release : 2021-05-08
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.

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 : 9780735502642
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.

Practical Instrumental Analysis

Practical Instrumental Analysis Book
Author : Manish Thimmaraju
Publisher : Unknown
Release : 2018-04-05
ISBN : 9781987576139
Language : En, Es, Fr & De

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Book Description :

The book Practical Instrumental Analysis is a genuine attempt to improve the practical knowledge of Pharm D students. The book is designed as per PCI regulations covering wide spectrum of Instrumental techniques like Spectroscopy, Colorimetric, Chromatography which includes Paper, Thin, Radial, Gradient &Isocratic HPLC, FTIR and Electrochemical analysis.The main objective of this book is to create interest in science of testing Active Pharmaceutical Ingredients and testing the purity in different dosage forms by various instrumental methods of analysis. Salient features of the book* Based on PCI prescribed syllabus for Pharm D* Provides basics of theory and practical in Instrumental analysis which includes principle and procedures.* To understand the different modern techniques of Pharmaceutical Analysis.* To appreciate the advantages of Instrumental methods in drug discovery.

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.

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.

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 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 Drug Analysis

Handbook of Drug Analysis Book
Author : Ray H. Liu,Daniel E. Gadzala
Publisher : Amer Chemical Society
Release : 1997
ISBN : 0987650XXX
Language : En, Es, Fr & De

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Book Description :

Covers preliminary test and chromatographic methods in forensic drug testing. Reviews identification methods such as molecular spectrophotometry, nuclear magnetic resonance, and mass spectrometry. Discusses the fundamental relationship between instrumentation and drug analysis. Evaluates the characteristics and pretreatment approaches for common sample categories. Presents in-depth test result interpretation on issues commonly encountered in workplace drug urinalysis. Analyzes and compares performance characteristics of immunoassays commonly used for workplace drug urinalysis.

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.

The British National Bibliography

The British National Bibliography Book
Author : Arthur James Wells
Publisher : Unknown
Release : 2002
ISBN : 0987650XXX
Language : En, Es, Fr & De

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Book Description :

Download The British National Bibliography book written by Arthur James Wells, available in PDF, EPUB, and Kindle, or read full book online anywhere and anytime. Compatible with any devices.

A Handbook of Bioanalysis and Drug Metabolism

A Handbook of Bioanalysis and Drug Metabolism Book
Author : Gary Evans
Publisher : CRC Press
Release : 2004-03-29
ISBN : 9780203642535
Language : En, Es, Fr & De

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Book Description :

Recent years have seen a greater industrial emphasis in undergraduate and postgraduate courses in the pharmaceutical and chemical sciences. However, textbooks have been slow to adapt, leaving the field without a text/reference that is both instructional and practical in the industrial setting – until now. A Handbook of Bioanalysis and Drug Metabolismis a stimulating new text that examines the techniques, methodology, and theory of bioanalysis, pharmacokinetics, and metabolism from the perspective of scientists with extensive professional experience in drug discovery and development. These three areas of research help drug developers to optimize the active component within potential drugs thereby increasing their effectiveness, and to provide safety and efficacy information required by regulators when granting a drug license. Professionals with extensive experience in drug discovery and development as well as specialized knowledge of the individual topics contributed to each chapter to create a current and well-credentialed text. It covers topics such as high performance liquid chromatography, protein binding, pharmacokinetics and drug–drug interactions. The unique industrial perspective helps to reinforce theory and develop valuable analytical and interpreting skills. This text is an invaluable guide to students in courses such as pharmaceutical science, pharmacology, chemistry, physiology and toxicology, as well as professionals in the biotechnology industry.

De structuur van wetenschappelijke revoluties

De structuur van wetenschappelijke revoluties Book
Author : Thomas S. Kuhn
Publisher : Boom Koninklijke Uitgevers
Release : 1972
ISBN : 9789060090671
Language : En, Es, Fr & De

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Book Description :

Download De structuur van wetenschappelijke revoluties book written by Thomas S. Kuhn, available in PDF, EPUB, and Kindle, or read full book online anywhere and anytime. Compatible with any devices.

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 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