Tag: Pharmaceutical

Free Download Paul J. Sheskey, Ph.D. Cook, Walter G., Ph.D. Cable, Colin G., "Handbook of Pharmaceutical Excipients"
English | 2017 | ISBN: 0857112716 | PDF | pages: 1216 | 272.3 mb
An internationally acclaimed reference work recognized as one of the most authoritative and comprehensive sources of information on excipients used in pharmaceutical formulation with this new edition providing 340 excipient monographs. Incorporates information on the uses, and chemical and physical properties of excipients systematically collated from a variety of international sources including: pharmacopeias, patents, primary and secondary literature, websites, and manufacturers’ data; extensive data provided on the applications, licensing, and safety of excipients; comprehensively cross-referenced and indexed, with many additional excipients described as related substances and an international supplier’s directory and detailed information on trade names and specific grades or types of excipients commercially available.

Free Download Andrew Lakoff, "Pharmaceutical Reason: Knowledge and Value in Global Psychiatry"
English | 2006 | pages: 218 | ISBN: 0521546664 | PDF | 1,6 mb
When a French biotechnology company seeks patients in Buenos Aires with bipolar disorder for its gene discovery program, they have unexpected trouble finding enough subjects for the study. In Argentina, the predominant form of mental health expertise – psychoanalysis – does not recognize the legitimacy of bipolar disorder as a diagnostic entity. This problem points to a broader set of political and epistemological debates in global psychiatry. Drawing from an ethnography of psychiatric practice in Buenos Aires, Andrew Lakoff follows the contested extension of novel techniques for understanding and intervening in mental illness. He charts the globalization of the new biomedical psychiatry, and illustrates the clashes, conflicts, alliances, and reformulations that take place when psychoanalytic and biological models of illness and cure meet. Highlighting the social and political implications that new forms of expertise about human behavior and thought bring, Lakoff presents an arresting case study that will appeal to scholars and students alike.

Free Download The Medical-Pharmaceutical Killing Machine: Facing Facts Could Save Your Life by Children’s Health Defense
English | November 26th, 2024 | ISBN: 1648211291 | 312 pages | True EPUB | 1.84 MB
Medical and pharmaceutical history is replete with examples of dangerous interventions that have poisoned, injured, or killed. However, events since 2020 have attracted attention as never before to medicine’s potential to be both lethal and malevolent. In The Medical-Pharmaceutical Killing Machine, Children’s Health Defense situates current perils in their broader context with the aim of helping readers understand how to protect themselves and their loved ones.

Free Download Modern Aspects of Pharmaceutical Quality Assurance: Developing & Proposing Application models, SOPs, practical audit systems for Pharma Industry by Minal Ghante, Manohar Potdar, Vidhya Bhusari
English | March 12, 2024 | ISBN: 9819992702 | 531 pages | MOBI | 14 Mb
The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.

Free Download 3D/4D Printing of Bioadhesive Pharmaceutical Systems
by Marcos Luciano Bruschi, Denise Tiemi Uchida, and Mariana Carla de Oliveira
English | 2025 | ISBN: 1032579269 | 164 pages | True PDF EPUB | 6.93 MB

Free Download Herbert Lieberman, "Pharmaceutical Dosage Forms: Disperse Systems"
English | 2019 | pages: 553 | ISBN: 036740060X | PDF | 14,4 mb
This third volume of the second edition offers information on specialized products such as emulsions, liposomes, polymers and polymeric pharmaceutical excipients. It explains the requirements for conducting clinical research and obtaining marketing approval for new drug products

Free Download Applications of Ion Chromatography for Pharmaceutical and Biological Products By
2012 | 455 Pages | ISBN: 0470467096 | PDF | 5 MB
This is a comprehensive source of information on the application of ion chromatography (IC) in the analysis of pharmaceutical drugs and biologicals. This book, with contributors from academia, pharma, the biotech industry, and instrument manufacturing, presents the different perspectives, experience, and expertise of the thought leaders of IC in a comprehensive manner. It explores potential IC applications in different aspects of product development and quality control testing. In addition, an appendix section gives information on critical physical and chromatographic parameters related to IC and information on current manufacturers of IC systems, columns, and other components.Content: Chapter 1 Ion Chromatography-Principles and Applications (pages 1-21): Lokesh BhattacharyyaChapter 2 Retention Processes in Ion?Exclusion Chromatography: A New Perspective (pages 23-47): Milko Novic and Paul R. HaddadChapter 3 Pulsed Electrochemical Detection in Ion Chromatography (pages 49-90): William R. LacourseChapter 4 Suppressor Design and Detection for Ion Chromatography (pages 91-105): Kannan Srinivasan, Sheetal Bhardwaj, Rong Lin and Christopher PohlChapter 5 Modelling and Optimization of Ion Chromatographic Separations of Pharmaceutically Relevant Organic Ions (pages 107-133): Philip Zakaria, Greg Dicinoski, Melissa Hanna?Brown and Paul R. HaddadChapter 6 Ion Chromatography in Pharmaceutical Drug Analysis (pages 135-157): Lokesh BhattacharyyaChapter 7 Analysis for Impurities by Ion Chromatography (pages 159-174): Shreekant V. KarmarkarChapter 8 Ion Chromatography Analysis of Aminoglycoside Antibiotics (pages 175-192): Valoran P. Hanko and Jeffrey S. RohrerChapter 9 Use of Cation?Exchange Ion Chromatography in the Analysis of Pharmaceuticals (pages 193-220): Christopher Pohl, Maria Rey and Rosanne SlingsbyChapter 11 High Performance Ion Chromatographic Analysis of Cholinergic Compounds: Carbachol and Bethanechol, and Associated Degradation Products (pages 237-245): David TrowbridgeChapter 12 Ion Chromatographic Analysis of Pharmaceuticals for Authenticity and Adulteration (pages 247-257): David S. JacksonChapter 13 Ion Chromatography of Drug Product Counter?Ions and other Ions in Drug Products (pages 259-269): Brian M. De Borba and Jeffrey S. RohrerChapter 14 Sample Preparation Techniques in Ion Chromatography for Pharmaceutical Applications (pages 271-283): Jay GandhiChapter 15 Validation of Ion Chromatographic Methods (pages 285-308): Shreekant V. KarmarkarChapter 16 Pharmacopeial Applications of Ion Chromatography (pages 309-320): Ravi RavichandranChapter 10 Comprehensive Approaches for Measurement of Active Pharmaceutical Ingredients, Counter?Ions, and Excipients Using HPLC with Charged Aerosol Detection (pages 221-236): Christopher Crafts, Bruce Bailey, Paul Gamache, Xiaodong Liu and Ian AcworthChapter 17 Glycan Analysis by High Performance Anion Exchange Chromatography with Pulsed Amperometric Detection (pages 321-338): Lokesh BhattacharyyaChapter 18 Monosaccharide Analysis of Glycoproteins by High?Performance Anion?Exchange Chromatography with Pulsed Amperometric Detection (pages 339-350): Jeffrey S. RohrerChapter 19 Two?Dimensional Ion Chromatography for Simultaneous Determination of Amino Acids and Carbohydrates (pages 351-364): Petr Jandik and Jun ChengChapter 20 Monitoring Protein N?Glycosylation Consistency Using HPAEC?PAD (pages 365-377): Carl GreyChapter 21 Oligosaccharide Analysis by High?Performance Anion?Exchange Chromatography Hyphenated to Integrated Pulsed Amperometric Detection and On?Line Ion?Trap Mass Spectrometry (pages 379-391): Cees BrugginkChapter 22 Applications of Ion Chromatography in Biological Product Analyses (pages 393-421): Alfred V. Del Grosso and Brandon DuongChapter 23 High Performance Anion?Exchange Chromatography with Pulsed Amperometric Detection (HPAEC?PAD) Analysis of GBS Glycoconjugate Vaccines: From Fermentation to Final Product (pages 423-434): Stefano Ricci, Barbara Fabbri, Sara Giannini, Silvia Bernardini, Marcello Morelli and Sandro D’AscenziChapter 24 Stability Studies and Characterization of Meningococcal A, C, Y, and W135 Glycoconjugate Vaccine (pages 435-447): Valeria Carinci, Alberto Bernardini, Cristiana Campa, Claudia Magagnoli, Francesca Beccai and Sandro D’Ascenzi

Free Download Mastering Pharmaceutical Quality Control From Zero To Hero
Published 9/2024
MP4 | Video: h264, 1920×1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 1.45 GB | Duration: 1h 32m
Focusing on pharmaceutical quality control, including physical and chemical tests, HPLC techniques and trouble shootings

Free Download Regulatory Aspects of Pharmaceutical Quality System: Brief Introduction by Arun Kumar Pandey
English | July 13, 2023 | ISBN: N/A | ASIN: B0CBTNZ368 | 371 pages | EPUB | 1.66 Mb
If you’re a B. Pharm or M. Pharm student seeking a comprehensive yet concise guide to the regulatory aspects of pharmaceutical quality systems, look no further than Regulatory Aspects of Pharmaceutical Quality System – Brief Introduction. While other textbooks on quality assurance cover a variety of topics to varying degrees of depth, this book provides a unified approach that is both insightful and practical. Designed to meet the needs of modern students and instructors, this book covers the basic guidelines and principles of quality assurance as they relate specifically to drug design, development, and evaluation. You’ll learn about the latest developments in the industry and how to apply these principles to the real-world challenges that you’re likely to encounter. Whether you’re a seasoned pharmaceutical professional or just starting out, you’ll find this book to be an invaluable resource that you’ll refer to time and time again.

Free Download The Textbook of Pharmaceutical Medicine, 6th Edition By
2009 | 766 Pages | ISBN: 1405180358 | PDF | 10 MB
The Textbook of Pharmaceutical Medicine is a standard reference for all those working in pharmaceutical medicine and the recognised text for the UK Faculty of Pharmaceutical Medicine Diploma. This is a comprehensive volume covering the processes by which medicines are developed, tested and approved. Regulations for drug development in the UK, EU, USA, Australia and Japan are discussed, providing relevant information for drug approval in the main continents where new drugs are developed. The chapters are written by leading academics, medical directors and lawyers, providing authoritative and in-depth information for trainees on the Faculty course, and for physicians working in the pharmaceutical industry. As well as thorough updating of the regulatory chapters, the 6th editionincludeschapters on these vital new areas: Paediatric regulationEthicsDue diligence and the pharmaceutical physicianContent: Chapter 1 Discovery of New Medicines (pages 1-80): Anand S. DuttaChapter 2 Pharmaceutical Development (pages 81-100): Gavin HalbertChapter 3 Preclinical Safety Testing (pages 101-136): Lutz Muller and Anke LuheChapter 4 Exploratory Development (pages 137-166): John PosnerChapter 5 Clinical Pharmacokinetics (pages 167-184): Paul Rolan and Valeria MolnarChapter 6 Purpose and Design of Clinical Trials (pages 185-206): Steve WarringtonChapter 7 Conduct of Clinical Trials: Good Clinical Practice (pages 207-239): Kate L. R. DarwinChapter 8 Medical Statistics (pages 240-269): Andrew P. GrieveChapter 9 Development of Medicines: Full Development (pages 270-284): Peter D. StonierChapter 10 The Medical Department (pages 285-295): Peter Stonier and David GillenChapter 11 Medical Marketing (pages 296-309): David Galloway and Bensita BernardChapter 12 Information and Promotion (pages 310-330): Charles de WetChapter 13 The Supply of Unlicensed Medicines for Individual Patient use (pages 331-346): Ian Dodds?Smith and Silvia ValverdeChapter 14 Human Experimentation – Ethics of First Human Exposure (pages 347-350): Duncan W. VereChapter 15 Legal and Ethical Issues Relating to Medicinal Products (pages 351-371): Nick Beckett, Sarah Hanson, Christopher J. S. Hodges and Shuna MasonChapter 16 The Safety of Medical Products (pages 372-409): A. Peter Fletcher and Susan ShawChapter 17 History of Drug Regulation in the UK (pages 411-443): John P. GriffinChapter 18 Regulation of Human Medicinal Products in the European Union (pages 444-499): Rashmi R. Shah and Agnes Saint RaymondChapter 19 Paediatric Regulation (pages 500-506): Heike RabeChapter 20 European Regulation of Medical Devices (pages 507-521): Christopher J. S. HodgesChapter 21 Technical Requirements for Registration of Pharmaceuticals for Human use: the ICH Process (pages 522-533): Dean W. G. HarronChapter 22 The Regulation of Drug Products by the US Food and Drug Administration (pages 534-566): Peter Barton HuttChapter 23 The US FDA in the Drug Development, Evaluation and Approval Process (pages 567-584): Richard N. Spivey, Judith K. Jones, William Wardell and William VodraChapter 24 Future Prospects of the Pharmaceutical Industry and its Regulation in the USA (pages 585-601): William Wardell, Judith K. Jones, Richard N. Spivey and William VodraChapter 25 Regulatory and Clinical Trial Systems in Japan (pages 602-612): Yuichi KuboChapter 26 The Regulation of Therapeutic Products in Australia (pages 613-640): Janice Hirshorn and Deborah MonkChapter 27 Pharmaceutical Medicine in the Emerging Markets (pages 641-657): Nadarajah Sreeharan and Jennie A. SykesChapter 28 Economics of Health Care (pages 661-673): Carole A. Bradley and Jane R. GriffinChapter 29 Controls on NHS Medicines Prescribing and Expenditure in the UK (a Historical Perspective) with some International Comparisons (pages 674-690): John P. Griffin and Jane R. GriffinChapter 30 Due Diligence and the Role of the Pharmaceutical Physician (pages 691-699): Geoffrey R. Barker