pharmaceutical poisonings



Nicolas Abatzoglou Pharmaceutical Blending and Mixing Nicolas Abatzoglou Pharmaceutical Blending and Mixing Новинка

Nicolas Abatzoglou Pharmaceutical Blending and Mixing

12652.88 руб.
Written in four parts, this book provides a dedicated and in-depth reference for blending within the pharmaceutical manufacturing industry. It links the science of blending with regulatory requirements associated with pharmaceutical manufacture. The contributors are a combination of leading academic and industrial experts, who provide an informed and industrially relevant perspective of the topic. This is an essential book for the pharmaceutical manufacturing industry, and related academic researchers in pharmaceutical science and chemical and mechanical engineering.
John Posner The Textbook of Pharmaceutical Medicine John Posner The Textbook of Pharmaceutical Medicine Новинка

John Posner The Textbook of Pharmaceutical Medicine

23767.36 руб.
The Textbook of Pharmaceutical Medicine is the standard reference for everyone working and learning in pharmaceutical medicine. It is a comprehensive resource covering the processes and practices by which medicines are developed, tested and approved, and the recognised text for the Diploma in Pharmaceutical Medicine from the Faculty of Pharmaceutical Medicine. This fully revised Seventh Edition, which includes two new Editors, encompasses current developments within pharmaceutical medicine with new chapters on biological therapeutics, pharmacovigilance, vaccines, drugs for cancer, drug development in paediatrics and neonatalogy, the clinical trials directive, life cycle management of medicines, counterfeit medicines and medical marketing. Also included for easy reference, and referred to throughout the text, are the Declaration of Helsinki, Guidelines and Documentation for Implementation of Clinical Trials, relevant European Directives and the Syllabus for Pharmaceutical Medicine. Written by an international team of leading academics, medical directors and lawyers, The Textbook of Pharmaceutical Medicine, Seventh Edition meets the needs of both those working in pharmaceutical medicine and preparing for the Diploma in Pharmaceutical Medicine. The text breaks down into three core sections: Part I: Research and Development Part II: Regulation Part III: Healthcare marketplace View Table of Contents in detail
John LaMattina L. Devalued and Distrusted. Can the Pharmaceutical Industry Restore its Broken Image? John LaMattina L. Devalued and Distrusted. Can the Pharmaceutical Industry Restore its Broken Image? Новинка

John LaMattina L. Devalued and Distrusted. Can the Pharmaceutical Industry Restore its Broken Image?

2530.29 руб.
An expert's view on solving the challenges confronting today's pharmaceutical industry Author John LaMattina, a thirty-year veteran of the pharmaceutical industry and former president of Pfizer's Global R&D Division, is internationally recognized as an expert on the pharmaceutical industry. His first book, Drug Truths: Dispelling the Myths About Pharma R&D, was critically acclaimed for clearing up misconceptions about the pharmaceutical industry and providing an honest account of the contributions of pharmaceutical research and development to human health and well-being. As he toured the country discussing Drug Truths, Dr. LaMattina regularly came across people who were filled with anger, accusing the pharmaceutical industry of making up diseases, hiding dangerous side effects, and more. This book was written in response to that experience, critically examining public perceptions and industry realities. Starting with «4 Secrets that Drug Companies Don't Want You to Know,» Devalued and Distrusted provides a fact-based account of how the pharmaceutical industry works and the challenges it faces. It addresses such critical issues as: Why pharmaceutical R&D productivity has declined Where pharmaceutical companies need to invest their resources What can be done to solve core health challenges, including cancer, diabetes, and neurodegenerative diseases How the pharmaceutical industry can regain public trust and resuscitate its image Our understanding of human health and disease grows daily; however, converting science into medicine is increasingly challenging. Reading Devalued and Distrusted, you'll not only gain a greater appreciation of those challenges, but also the role that the pharmaceutical industry currently plays and can play in solving those challenges. Get to know the author: Read an interview with John LaMattina or watch a video on ChemistryViews! Interview: John LaMattina: 30 Years in Pharma Video: Can the Pharmaceutical Industry Restory its Broken Image?
Stig Pedersen-Bjergaard Introduction to Pharmaceutical Chemical Analysis Stig Pedersen-Bjergaard Introduction to Pharmaceutical Chemical Analysis Новинка

Stig Pedersen-Bjergaard Introduction to Pharmaceutical Chemical Analysis

16516.11 руб.
This textbook is the first to present a systematic introduction to chemical analysis of pharmaceutical raw materials, finished pharmaceutical products, and of drugs in biological fluids, which are carried out in pharmaceutical laboratories worldwide. In addition, this textbook teaches the fundamentals of all the major analytical techniques used in the pharmaceutical laboratory, and teaches the international pharmacopoeias and guidelines of importance for the field. It is primarily intended for the pharmacy student, to teach the requirements in “analytical chemistry” for the 5 years pharmacy curriculum, but the textbook is also intended for analytical chemists moving into the field of pharmaceutical analysis. Addresses the basic concepts, then establishes the foundations for the common analytical methods that are currently used in the quantitative and qualitative chemical analysis of pharmaceutical drugs Provides an understanding of common analytical techniques used in all areas of pharmaceutical development Suitable for a foundation course in chemical and pharmaceutical sciences Aimed at undergraduate students of degrees in Pharmaceutical Science/Chemistry Analytical Science/Chemistry, Forensic analysis Includes many illustrative examples
Norman Hodges A. Hugo and Russell's Pharmaceutical Microbiology Norman Hodges A. Hugo and Russell's Pharmaceutical Microbiology Новинка

Norman Hodges A. Hugo and Russell's Pharmaceutical Microbiology

6787.74 руб.
Pharmaceutical microbiology has a bearing on all aspects of pharmacy, from the manufacture and quality control of pharmaceutical products through to an understanding of the mode of action of antibiotics. Fully revised and restructured, drawing on the contributions of subject experts, and including material relevant to the European curricula in pharmacy, the eighth edition covers: biology of micro-organisms pathogens and host response prescribing therapeutics contamination and infection control pharmaceutical production current trends and new directions Hugo and Russell’s Pharmaceutical Microbiology, a standard text for Schools of Pharmacy for seven editions, continues to be a user-friendly and authoritative guide for both students and practitioners of pharmacy and pharmaceutical microbiology. 'Highly Commended' in the Pharmacology section of the 2012 BMA Book Awards
Gaisford Simon Essentials of Pharmaceutical Preformulation Gaisford Simon Essentials of Pharmaceutical Preformulation Новинка

Gaisford Simon Essentials of Pharmaceutical Preformulation

12275.27 руб.
Essentials of Pharmaceutical Preformulation is a study guide which describes the basic principles of pharmaceutical physicochemical characterisation. Successful preformulation requires knowledge of fundamental molecular concepts (solubility, ionisation, partitioning, hygroscopicity and stability) and macroscopic properties (physical form, such as the crystalline and amorphous states, hydrates, solvates and co-crystals and powder properties), familiarity with the techniques used to measure them and appreciation of their effect on product performance, recognising that often there is a position of compromise to be reached between product stability and bioavailability. This text introduces the basic concepts and discusses their wider implication for pharmaceutical development, with reference to many case examples of current drugs and drug products. Special attention is given to the principles and best-practice of the analytical techniques that underpin preformulation (UV spectrophotometry, TLC, DSC, XRPD and HPLC). The material is presented in the typical order that would be followed when developing a medicine and maps onto the indicative pharmacy syllabus of the Royal Pharmaceutical Society of Great Britain Undergraduate-level pharmacy students and R&D / analytical scientists working in the pharmaceutical sector (with or without a pharmaceutical background) will find this text easy to follow with relevant pharmaceutical examples. Essential study guide for pharmacy and pharmaceutical science students Covers the pharmaceutical preformulation components of the Royal Pharmaceutical Society of Great Britain’s indicative syllabus Easy to follow text highlighted with relevant pharmaceutical examples Self-assessment assignments in a variety of formats Written by authors with both academic and industrial experience Companion website with further information to maximise learning
Takayuki Shioiri Pharmaceutical Process Chemistry Takayuki Shioiri Pharmaceutical Process Chemistry Новинка

Takayuki Shioiri Pharmaceutical Process Chemistry

17673.76 руб.
Covering the whole area of process chemistry in the pharmaceutical industry, this monograph provides the essential knowledge on the basic chemistry needed for future development and key industrial techniques, as well as morphology, engineering and regulatory compliances. Application-oriented and well structured, the authors include recent examples of excellent industrial production of active pharmaceutical ingredients.
Yuriy Abramov A. Computational Pharmaceutical Solid State Chemistry Yuriy Abramov A. Computational Pharmaceutical Solid State Chemistry Новинка

Yuriy Abramov A. Computational Pharmaceutical Solid State Chemistry

11572.85 руб.
This book is the first to combine computational material science and modeling of molecular solid states for pharmaceutical industry applications. • Provides descriptive and applied state-of-the-art computational approaches and workflows to guide pharmaceutical solid state chemistry experiments and to support/troubleshoot API solid state selection • Includes real industrial case examples related to application of modeling methods in problem solving • Useful as a supplementary reference/text for undergraduate, graduate and postgraduate students in computational chemistry, pharmaceutical and biotech sciences, and materials science
Shayne Cox Gad Pharmaceutical Manufacturing Handbook Shayne Cox Gad Pharmaceutical Manufacturing Handbook Новинка

Shayne Cox Gad Pharmaceutical Manufacturing Handbook

18897.45 руб.
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Otilia M. Y. Koo Pharmaceutical Excipients. Properties, Functionality, and Applications in Research and Industry Otilia M. Y. Koo Pharmaceutical Excipients. Properties, Functionality, and Applications in Research and Industry Новинка

Otilia M. Y. Koo Pharmaceutical Excipients. Properties, Functionality, and Applications in Research and Industry

13505.93 руб.
This book provides an overview of excipients, their functionalities in pharmaceutical dosage forms, regulation, and selection for pharmaceutical products formulation. It includes development, characterization methodology, applications, and up-to-date advances through the perspectives of excipients developers, users, and regulatory experts. Covers the sources, characterization, and harmonization of excipients: essential information for optimal excipients selection in pharmaceutical development Describes the physico-chemical properties and biological effects of excipients Discusses chemical classes, safety and toxicity, and formulation Addresses recent efforts in the standardization and harmonization of excipients
William Lewis The Edinburgh New Dispensatory: Containing I. the Elements of Pharmaceutical Chemistry. Ii. the Materia Medica; Or, the Natural, Pharmaceutical, and . Iii. the Pharmaceutical Preparations an William Lewis The Edinburgh New Dispensatory: Containing I. the Elements of Pharmaceutical Chemistry. Ii. the Materia Medica; Or, the Natural, Pharmaceutical, and . Iii. the Pharmaceutical Preparations an Новинка

William Lewis The Edinburgh New Dispensatory: Containing I. the Elements of Pharmaceutical Chemistry. Ii. the Materia Medica; Or, the Natural, Pharmaceutical, and . Iii. the Pharmaceutical Preparations an

1204 руб.
Эта книга — репринт оригинального издания, созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Andreas Cmolik Threats and Opportunities for European Pharmaceutical Wholesalers in a Changing Healthcare Environment Andreas Cmolik Threats and Opportunities for European Pharmaceutical Wholesalers in a Changing Healthcare Environment Новинка

Andreas Cmolik Threats and Opportunities for European Pharmaceutical Wholesalers in a Changing Healthcare Environment

7127 руб.
The aim of this book is to identify the major drivers of change within the European healthcare systems and to evaluate risks and opportunities confronting pharmaceutical full-line wholesalers. These businesses are the most important link between pharmaceutical manufacturing and the point of sale; providing one-stop-shopping for healthcare professionals across Europe.While on the one hand European governments are interested to ensure broad access to healthcare provision for the general public with a high level of quality, they are on the other hand concerned with limiting cost increases and with the need to cap healthcare spending.In addition, the pharmaceutical industry faces a strong need to cut costs by outsourcing non-core activities and establishing new routes to the customer, often bypassing the established supply chain.Changing healthcare environments across Europe ask for new strategies of pharmaceutical wholesalers to be fit for the future. This book deals with the advantages that can be derived from the changing landscape of healthcare provision.Aging populations, markets in transition, outsourcing activities of manufacturers and legal changes provide the potential to turn threats into opportunities and further develop the business model of pharmaceutical wholesaling. Even with profound structural changes in healthcare systems, pharmaceutical wholesalers are provided with significant potential to remain a vital part of the pharmaceutical supply chain and to prosper i...
Philip Rowe Essential Statistics for the Pharmaceutical Sciences Philip Rowe Essential Statistics for the Pharmaceutical Sciences Новинка

Philip Rowe Essential Statistics for the Pharmaceutical Sciences

10544.07 руб.
Essential Statistics for the Pharmaceutical Sciences is targeted at all those involved in research in pharmacology, pharmacy or other areas of pharmaceutical science; everybody from undergraduate project students to experienced researchers should find the material they need. This book will guide all those who are not specialist statisticians in using sound statistical principles throughout the whole journey of a research project – designing the work, selecting appropriate statistical methodology and correctly interpreting the results. It deliberately avoids detailed calculation methodology. Its key features are friendliness and clarity. All methods are illustrated with realistic examples from within pharmaceutical science. This edition now includes expanded coverage of some of the topics included in the first edition and adds some new topics relevant to pharmaceutical research. a clear, accessible introduction to the key statistical techniques used within the pharmaceutical sciences all examples set in relevant pharmaceutical contexts. key points emphasised in summary boxes and warnings of potential abuses in ‘pirate boxes’. supplementary material – full data sets and detailed instructions for carrying out analyses using packages such as SPSS or Minitab – provided at www.ljmu.ac.uk/pbs/rowestats/ An invaluable introduction to statistics for any science student and an essential text for all those involved in pharmaceutical research at whatever level.
Lionel Edwards D. Principles and Practice of Pharmaceutical Medicine Lionel Edwards D. Principles and Practice of Pharmaceutical Medicine Новинка

Lionel Edwards D. Principles and Practice of Pharmaceutical Medicine

27784.35 руб.
The new edition of Principles and Practice of Pharmaceutical Medicine is a comprehensive reference guide to all aspects of pharmaceutical medicine. New content includes chapters and coverage on regulatory updates, increasing international harmonization, transitional and probabilistic approaches to drug development, the growing sophistication and regulatory importance of pharmacovigilance, personalized medicine and growth in biotechnology as a source of new experimental drugs.
Behnam Davani Pharmaceutical Analysis for Small Molecules Behnam Davani Pharmaceutical Analysis for Small Molecules Новинка

Behnam Davani Pharmaceutical Analysis for Small Molecules

9647.09 руб.
A comprehensive introduction for scientists engaged in new drug development, analysis, and approvals Each year the pharmaceutical industry worldwide recruits thousands of recent science graduates—especially chemistry, analytical chemistry, pharmacy, and pharmaceutical majors—into its ranks. However, because of their limited background in pharmaceutical analysis most of those new recruits find making the transition from academia to industry very difficult. Designed to assist both recent graduates, as well as experienced chemists or scientists with limited regulatory, compendial or pharmaceutical analysis background, make that transition, Pharmaceutical Analysis for Small Molecules is a concise, yet comprehensive introduction to the drug development process and analysis of chemically synthesized, small molecule drugs. It features contributions by distinguished experts in the field, including editor and author, Dr. Behnam Davani, an analytical chemist with decades of technical management and teaching experience in compendial, regulatory, and industry. This book provides an introduction to pharmaceutical analysis for small molecules (non-biologics) using commonly used techniques for drug characterization and performance tests. The driving force for industry to perform pharmaceutical analyses is submission of such data and supporting documents to regulatory bodies for drug approval in order to market their products. In addition, related required supporting studies including good laboratory/documentation practices including analytical instrument qualification are highlighted in this book. Topics covered include: Drug Approval Process and Regulatory Requirements (private standards) Pharmacopeias and Compendial Approval Process (public standards) Common methods in pharmaceutical analysis (typically compendial) Common Calculations for assays and impurities and other specific tests Analytical Method Validation, Verification, Transfer Specifications including how to handle out of specification (OOS) and out of trend (OOT) Impurities including organic, inorganic, residual solvents and elemental impurities Good Documentation Practices for regulatory environment Management of Analytical Laboratories Analytical Instrument Qualifications including IQ, OQ, PQ and VQ Due to global nature of pharmaceutical industry, other topics on both regulatory (ICH) and Compendial harmonization are also highlighted. Pharmaceutical Analysis for Small Molecules is a valuable working resource for scientists directly or indirectly involved with the drug development process, including analytical chemists, pharmaceutical scientists, pharmacists, and quality control/quality assurance professionals. It also is an excellent text/reference for graduate students in analytical chemistry, pharmacy, pharmaceutical and regulatory sciences.
Dipak Kumar Sarker Pharmaceutical Emulsions. A Drug Developer's Toolbag Dipak Kumar Sarker Pharmaceutical Emulsions. A Drug Developer's Toolbag Новинка

Dipak Kumar Sarker Pharmaceutical Emulsions. A Drug Developer's Toolbag

10033.71 руб.
Pharmaceutical Emulsions: A Drug Developer's Toolbag covers all the key aspects of pharmaceutical emulsions, starting from the fundamental scientific basics, to the pharmaceutical forms and the chemical tests for its application. The author uses his extensive experience in both industry and academic experience to provide a concise, student friendly guide to the essential fundamentals of physical pharmacy. Divided into three clear sections, the text begins with Section A – Consideration for Product: Medicinal Formulation which includes a historical perspective, explanation of what is an emulsion, stability and instability, and manufacture. Section B – Forms, Use and Application follows, with chapters on creams and ointments, pastes and bases, colloids, transdermal, gels and implants. The final Section, Tests: Chemistry to control the quality, efficacy and fitness for purpose of the product includes chapters on physic-chemical properties, sizing and microscopy, rheology, QC and finally questions, calculations and dilemmas. Throughout the text there are numerous figures, diagrams and tables to engage the reader. This is an invaluable reference for all students of pharmaceutical sciences, pharmacy industrial pharmaceutical sciences, physical pharmacy and pharmaceutical forms as well as industry professionals
Dennis Douroumis Hot-Melt Extrusion. Pharmaceutical Applications Dennis Douroumis Hot-Melt Extrusion. Pharmaceutical Applications Новинка

Dennis Douroumis Hot-Melt Extrusion. Pharmaceutical Applications

15205.5 руб.
Hot-melt extrusion (HME) – melting a substance and forcing it through an orifice under controlled conditions to form a new material – is an emerging processing technology in the pharmaceutical industry for the preparation of various dosage forms and drug delivery systems, for example granules and sustained release tablets. Hot-Melt Extrusion: Pharmaceutical Applications covers the main instrumentation, operation principles and theoretical background of HME. It then focuses on HME drug delivery systems, dosage forms and clinical studies (including pharmacokinetics and bioavailability) of HME products. Finally, the book includes some recent and novel HME applications, scale -up considerations and regulatory issues. Topics covered include: principles and die design of single screw extrusion twin screw extrusion techniques and practices in the laboratory and on production scale HME developments for the pharmaceutical industry solubility parameters for prediction of drug/polymer miscibility in HME formulations the influence of plasticizers in HME applications of polymethacrylate polymers in HME HME of ethylcellulose, hypromellose, and polyethylene oxide bioadhesion properties of polymeric films produced by HME taste masking using HME clinical studies, bioavailability and pharmacokinetics of HME products injection moulding and HME processing for pharmaceutical materials laminar dispersive & distributive mixing with dissolution and applications to HME technological considerations related to scale-up of HME processes devices and implant systems by HME an FDA perspective on HME product and process understanding improved process understanding and control of an HME process with near-infrared spectroscopy Hot-Melt Extrusion: Pharmaceutical Applications is an essential multidisciplinary guide to the emerging pharmaceutical uses of this processing technology for researchers in academia and industry working in drug formulation and delivery, pharmaceutical engineering and processing, and polymers and materials science. This is the first book from our brand new series Advances in Pharmaceutical Technology. Find out more about the series here.
Dennis Jenke Compatibility of Pharmaceutical Solutions and Contact Materials. Safety Assessments of Extractables and Leachables for Pharmaceutical Products Dennis Jenke Compatibility of Pharmaceutical Solutions and Contact Materials. Safety Assessments of Extractables and Leachables for Pharmaceutical Products Новинка

Dennis Jenke Compatibility of Pharmaceutical Solutions and Contact Materials. Safety Assessments of Extractables and Leachables for Pharmaceutical Products

11087.34 руб.
Compatibility of Pharmaceutical Products and Contact Materials Dennis Jenke Important safety aspects of compatibility for therapeutic products and their manufacturing systems, delivery devices, and containers Compatibility of Pharmaceutical Products and Contact Materials helps pharmaceutical, toxicology, analytical, and regulatory affairs professionals assess the safety of leachable and extractable chemicals associated with drug product packaging, manufacturing systems, and devices. The most comprehensive resource available, its coverage includes the strategies, tactics, and regulatory requirements for performing safety assessments, along with the means for interpreting results. Structured around a logical framework for an extractables and leachables safety assessment and closely linked to the pharmaceutical product development process, Compatibility of Pharmaceutical Products and Contact Materials directly addresses the fundamental questions of «what activities need to be performed to completely, efficiently, and effectively address the issue of product safety from an extractables and leachables perspective?» and «when do the various required activities need to be performed?» Specifically, the chapters describe: Pertinent regulations and practical ways to meet guidelines Coordinating manufacturing, storage, and delivery systems development and qualification with therapeutic product development Materials characterization and the materials screening process Component and/or system qualification (illustrated by several case studies) Performing validation/migration studies and interpreting and reporting the results Creating a product registration dossier and putting it through regulatory review Product maintenance (Change Control) from an extractables and leachables perspective Likely future developments in extractables and leachables assessment Additionally, the book's appendix provides a database, including CAS registry numbers, chemical formulas and molecular weights of extractable/leachable substances that have been reported in the chemical literature. Detailing the interconnected roles played by analytical chemistry, biological science, toxicology, and regulatory science, Compatibility of Pharmaceutical Products and Contact Materials supplies a much-needed, comprehensive resource to all those in pharmaceutical product or medical device development.
Alessandra Mattei Pharmaceutical Crystals. Science and Engineering Alessandra Mattei Pharmaceutical Crystals. Science and Engineering Новинка

Alessandra Mattei Pharmaceutical Crystals. Science and Engineering

14849.12 руб.
An important resource that puts the focus on understanding and handling of organic crystals in drug development Since a majority of pharmaceutical solid-state materials are organic crystals, their handling and processing are critical aspects of drug development. Pharmaceutical Crystals: Science and Engineering offers an introduction to and thorough coverage of organic crystals, and explores the essential role they play in drug development and manufacturing. Written contributions from leading researchers and practitioners in the field, this vital resource provides the fundamental knowledge and explains the connection between pharmaceutically relevant properties and the structure of a crystal. Comprehensive in scope, the text covers a range of topics including: crystallization, molecular interactions, polymorphism, analytical methods, processing, and chemical stability. The authors clearly show how to find solutions for pharmaceutical form selection and crystallization processes. Designed to be an accessible guide, this book represents a valuable resource for improving the drug development process of small drug molecules. This important text: Includes the most important aspects of solid-state organic chemistry and its role in drug development Offers solutions for pharmaceutical form selection and crystallization processes Contains a balance between the scientific fundamental and pharmaceutical applications Presents coverage of crystallography, molecular interactions, polymorphism, analytical methods, processing, and chemical stability Written for both practicing pharmaceutical scientists, engineers, and senior undergraduate and graduate students studying pharmaceutical solid-state materials, Pharmaceutical Crystals: Science and Engineering is a reference and textbook for understanding, producing, analyzing, and designing organic crystals which is an imperative skill to master for anyone working in the field.
Ekins Sean Pharmaceutical Data Mining. Approaches and Applications for Drug Discovery Ekins Sean Pharmaceutical Data Mining. Approaches and Applications for Drug Discovery Новинка

Ekins Sean Pharmaceutical Data Mining. Approaches and Applications for Drug Discovery

12671.25 руб.
Leading experts illustrate how sophisticated computational data mining techniques can impact contemporary drug discovery and development In the era of post-genomic drug development, extracting and applying knowledge from chemical, biological, and clinical data is one of the greatest challenges facing the pharmaceutical industry. Pharmaceutical Data Mining brings together contributions from leading academic and industrial scientists, who address both the implementation of new data mining technologies and application issues in the industry. This accessible, comprehensive collection discusses important theoretical and practical aspects of pharmaceutical data mining, focusing on diverse approaches for drug discovery—including chemogenomics, toxicogenomics, and individual drug response prediction. The five main sections of this volume cover: A general overview of the discipline, from its foundations to contemporary industrial applications Chemoinformatics-based applications Bioinformatics-based applications Data mining methods in clinical development Data mining algorithms, technologies, and software tools, with emphasis on advanced algorithms and software that are currently used in the industry or represent promising approaches In one concentrated reference, Pharmaceutical Data Mining reveals the role and possibilities of these sophisticated techniques in contemporary drug discovery and development. It is ideal for graduate-level courses covering pharmaceutical science, computational chemistry, and bioinformatics. In addition, it provides insight to pharmaceutical scientists, principal investigators, principal scientists, research directors, and all scientists working in the field of drug discovery and development and associated industries.
David J. am Ende Chemical Engineering in the Pharmaceutical Industry. R&D to Manufacturing David J. am Ende Chemical Engineering in the Pharmaceutical Industry. R&D to Manufacturing Новинка

David J. am Ende Chemical Engineering in the Pharmaceutical Industry. R&D to Manufacturing

18131.77 руб.
This book deals with various unique elements in the drug development process within chemical engineering science and pharmaceutical R&D. The book is intended to be used as a professional reference and potentially as a text book reference in pharmaceutical engineering and pharmaceutical sciences. Many of the experimental methods related to pharmaceutical process development are learned on the job. This book is intended to provide many of those important concepts that R&D Engineers and manufacturing Engineers should know and be familiar if they are going to be successful in the Pharmaceutical Industry. These include basic analytics for quantitation of reaction components– often skipped in ChE Reaction Engineering and kinetics books. In addition Chemical Engineering in the Pharmaceutical Industry introduces contemporary methods of data analysis for kinetic modeling and extends these concepts into Quality by Design strategies for regulatory filings. For the current professionals, in-silico process modeling tools that streamline experimental screening approaches is also new and presented here. Continuous flow processing, although mainstream for ChE, is unique in this context given the range of scales and the complex economics associated with transforming existing batch-plant capacity. The book will be split into four distinct yet related parts. These parts will address the fundamentals of analytical techniques for engineers, thermodynamic modeling, and finally provides an appendix with common engineering tools and examples of their applications.
Obinna Ekwunife Pharmaceutical Care Program in a Nigerian Pharmacy Obinna Ekwunife Pharmaceutical Care Program in a Nigerian Pharmacy Новинка

Obinna Ekwunife Pharmaceutical Care Program in a Nigerian Pharmacy

8652 руб.
This single-centre study was designed to assess the impact of a pharmaceutical care program in a Nigerian pharmacy. Patients underwent 5 months of usual care and another 5 months of pharmaceutical care. During pharmaceutical care intervention, patients received a face-to-face, goal-directed medication and lifestyle counselling once a month. Blood pressure and quality of life measured before implementation of pharmaceutical care and at the end served as main outcome measures. Other outcomes were also assessed. Twenty four (24) patients out of the 40 recruited completed the study. There were significant reductions in the mean values for systolic blood pressure (14.3 mmHg), diastolic blood pressure (10.8 mmHg) and alcohol misuse (33.3%) after pharmaceutical care intervention. There was a positive increase of -11.4 and -3.2 for physical health and social health domain of quality of life evaluation respectively. Pharmaceutical care programme for hypertensive patients provided in a Nigerian community pharmacy produced beneficial reduction in blood pressure and improved the health related quality of life of the patients.
фуцикорт крем 15 г фуцикорт крем 15 г Новинка
джосет сироп 100 мл джосет сироп 100 мл Новинка
DR AR PARADKAR INTRODUCTION TO PHARMACEUTICAL ENGINEERING DR AR PARADKAR INTRODUCTION TO PHARMACEUTICAL ENGINEERING Новинка

DR AR PARADKAR INTRODUCTION TO PHARMACEUTICAL ENGINEERING

3964 руб.
Introduction - Flow of Fluids - Heat Transfer - Mass Transfer - Size Reduction - Size Separation - Filtration - Mixing - Extraction - Crystallization - Evaporation - Drying - Distillation - Pumps - Transportation of Solids - Corrosion - Fire Hazards - Pollution From Pharmaceutical Industry - Conversion Tables - Index
йокс раствор 50 мл йокс раствор 50 мл Новинка
Abdel-Kader Nora S., El-Ansary Aida L., Asran Amal M. Spectrophotometric determination of diaveridine and two sulfa drugs Abdel-Kader Nora S., El-Ansary Aida L., Asran Amal M. Spectrophotometric determination of diaveridine and two sulfa drugs Новинка

Abdel-Kader Nora S., El-Ansary Aida L., Asran Amal M. Spectrophotometric determination of diaveridine and two sulfa drugs

9739 руб.
Analytical chemistry is very important in pharmaceutical industries, where without quality assurance, the pharmaceutical preparations can't be performed. Thus, the analyst needs a rapid, easy, inexpensive, sensitive, selective and accurate method of analysis, these properties can be achieved by the use of spectrophotometery for quantitative analysis of pharmaceutical compounds. Several spectrophotometric methods are in use in pharmaceutical analysis. For a long time direct UV-measurements have been used as the official and pharmacopoeias methods. Spectrophotometric methods applied in pharmaceutical analysis are numerous; mostly all spectral methods are in use. Among these, is molecular spectrophotometric method using UV and visible radiation.This book contains the development of fast, cheap, accurate and sensitive spectrophotometric techniques for the determination of diaveridine, sulfadimidine and sulfaguanidine in pure forms and in some commercial pharmaceutical preparations.the proposed spectrophotometric techniques have advantages over many of the reported methods due to their sensitivity, wide application and they need inexpensive sophisticated apparatus.
Jack Shostak SAS Programming in the Pharmaceutical Industry, Second Edition Jack Shostak SAS Programming in the Pharmaceutical Industry, Second Edition Новинка

Jack Shostak SAS Programming in the Pharmaceutical Industry, Second Edition

6202 руб.
This comprehensive resource provides on-the-job training for statistical programmers who use SAS in the pharmaceutical industryThis one-stop resource offers a complete review of what entry- to intermediate-level statistical programmers need to know in order to help with the analysis and reporting of clinical trial data in the pharmaceutical industry. SAS Programming in the Pharmaceutical Industry, Second Edition begins with an introduction to the pharmaceutical industry and the work environment of a statistical programmer. Then it gives a chronological explanation of what you need to know to do the job. It includes information on importing and massaging data into analysis data sets, producing clinical trial output, and exporting data. This edition has been updated for SAS 9.4, and it features new graphics as well as all new examples using CDISC SDTM or ADaM model data structures.Whether you're a novice seeking an introduction to SAS programming in the pharmaceutical industry or a junior-level programmer exploring new approaches to problem solving, this real-world reference guide offers a wealth of practical suggestions to help you sharpen your skills. This book is part of the SAS Press program.
Stefan Kirchner Pharmaceutical Intellectual Property Rights and the Single Market Stefan Kirchner Pharmaceutical Intellectual Property Rights and the Single Market Новинка

Stefan Kirchner Pharmaceutical Intellectual Property Rights and the Single Market

2689 руб.
Thesis (M.A.) from the year 2006 in the subject Law - European and International Law, Intellectual Properties, grade: 13,53 (gut) , Justus-Liebig-University Giessen, course: Magister Juris Internationalis, language: English, abstract: With an aging demographic all over the European Union, the European pharmaceutical sector is set to grow in the coming decades. Al-ready today the pharmaceutical industry is a key employer in Europe. At the same time, the pharmaceutical industry is marked by a very ex-pensive research and development phase, which makes strong intellectual property rights crucial to ensure that research for new pharmaceuticals remains commercially interesting. But not only direct threats to intellectual property rights, such as the production of generic phar-maceuticals or the sale of counterfeit pharmaceuticals, pose a threat to those pharmaceutical companies which heavily invest in research for the development of new products: different prices for identical pharmaceuticals in different member states of the European Community make it economically interesting to buy pharmaceuticals in one member state and sell them abroad. It might even be cheaper to sell reimported pharmaceuticals in the country of origin. This possibility opens a whole new market for reimporters which cuts directly into the profit of the producers. In this thesis we will look at different issues surrounding intellectual property rights in the European pharmaceutical sector by investigating the ...
Iqbal Muhammad Naeem, Mughal Naz, Wang Shihua Sterility testing and toxin detection Iqbal Muhammad Naeem, Mughal Naz, Wang Shihua Sterility testing and toxin detection Новинка

Iqbal Muhammad Naeem, Mughal Naz, Wang Shihua Sterility testing and toxin detection

6027 руб.
A sterility test may be defined as - 'a test that critically assesses whether a sterilized pharmaceutical product is free from contaminating microorganisms'. Pharmaceutical products were tested for contamination and the presence of toxins. Various methods were used for this purpose. The objective of this study is to determine whether the pharmaceutical products in the markets are sterile and free of toxins.
Axel Jörn Pfizer and the Challenges of the Global Pharmaceutical Industry Axel Jörn Pfizer and the Challenges of the Global Pharmaceutical Industry Новинка

Axel Jörn Pfizer and the Challenges of the Global Pharmaceutical Industry

3214 руб.
This Case Study defines the global pharmaceutical industry and its „boundaries", analyses the profitability/attractiveness of the global pharmaceutical industry by using M.E.Porters' Five-Forces-Model and answers the questions what overall industry trends can be identified and how the profitability/attractiveness of the industry will change in the future. Furthermore it explains and evaluates Pfizer's new strategy and examines what Pfizer did in the recent years to maintain their profitability.
Gary Prager Practical Pharmaceutical Engineering Gary Prager Practical Pharmaceutical Engineering Новинка

Gary Prager Practical Pharmaceutical Engineering

13304.81 руб.
A practical guide to all key the elements of pharmaceuticals and biotech manufacturing and design Engineers working in the pharmaceutical and biotech industries are routinely called upon to handle operational issues outside of their fields of expertise. Traditionally the competencies required to fulfill those tasks were achieved piecemeal, through years of self-teaching and on-the-job experience—until now. Practical Pharmaceutical Engineering provides readers with the technical information and tools needed to deal with most common engineering issues that can arise in the course of day-to-day operations of pharmaceutical/biotech research and manufacturing. Engineers working in pharma/biotech wear many hats. They are involved in the conception, design, construction, and operation of research facilities and manufacturing plants, as well as the scale-up, manufacturing, packaging, and labeling processes. They have to implement FDA regulations, validation assurance, quality control, and Good Manufacturing Practices (GMP) compliance measures, and to maintain a high level of personal and environmental safety. This book provides readers from a range of engineering specialties with a detailed blueprint and the technical knowledge needed to tackle those critical responsibilities with confidence. At minimum, after reading this book, readers will have the knowledge needed to constructively participate in contractor/user briefings. Provides pharmaceutical industry professionals with an overview of how all the parts fit together and a level of expertise that can take years of on-the-job experience to acquire Addresses topics not covered in university courses but which are crucial to working effectively in the pharma/biotech industry Fills a gap in the literature, providing important information on pharmaceutical operation issues required for meeting regulatory guidelines, plant support design, and project engineering Covers the basics of HVAC systems, water systems, electric systems, reliability, maintainability, and quality assurance, relevant to pharmaceutical engineering Practical Pharmaceutical Engineering is an indispensable “tool of the trade” for chemical engineers, mechanical engineers, and pharmaceutical engineers employed by pharmaceutical and biotech companies, engineering firms, and consulting firms. It also is a must-read for engineering students, pharmacy students, chemistry students, and others considering a career in pharmaceuticals.
Innovation in the Pharmaceutical Industry: The Process of Drug Discovery and Development Innovation in the Pharmaceutical Industry: The Process of Drug Discovery and Development Новинка

Innovation in the Pharmaceutical Industry: The Process of Drug Discovery and Development

13433 руб.
Book DescriptionInnovation in the Pharmaceutical Industry traces the discovery and development of drugs in Japan and the UK both historically and sociologically. It includes sixteen case studies of major pharmaceutical developments in the twentieth century, encompassing, among others, beta-blockers, beta-stimulants, inhaled steroids and histamine H2-antagonists. The book illustrates that the four stages of drug development - namely compound, application, organizational authorization and market - are interactively shaped by heterogeneous actors and institutions. The book also identifies three different types of pharmaceutical development - paradigmatic innovation, application innovation and modification-based innovation, all with distinguishable features in the drug development process. Finally, several historical, structural and cultural factors influencing the shaping of medicines are revealed by the comparison between British and Japanese drug innovation. Addressing a number of practical implications for the promotion of the pharmaceutical industry, this book will be of enormous interest to students, researchers and academics specializing in science and technology, and the management of technology and innovation. Practitioners, managers, and policy planners within the pharmaceutical industry will also deem this book invaluable.
Katja Strohfeldt A. Essentials of Inorganic Chemistry. For Students of Pharmacy, Pharmaceutical Sciences and Medicinal Chemistry Katja Strohfeldt A. Essentials of Inorganic Chemistry. For Students of Pharmacy, Pharmaceutical Sciences and Medicinal Chemistry Новинка

Katja Strohfeldt A. Essentials of Inorganic Chemistry. For Students of Pharmacy, Pharmaceutical Sciences and Medicinal Chemistry

5543.67 руб.
A comprehensive introduction to inorganic chemistry and, specifically, the science of metal-based drugs, Essentials of Inorganic Chemistry describes the basics of inorganic chemistry, including organometallic chemistry and radiochemistry, from a pharmaceutical perspective. Written for students of pharmacy and pharmacology, pharmaceutical sciences, medicinal chemistry and other health-care related subjects, this accessible text introduces chemical principles with relevant pharmaceutical examples rather than as stand-alone concepts, allowing students to see the relevance of this subject for their future professions. It includes exercises and case studies.
Marc Descamps Disordered Pharmaceutical Materials Marc Descamps Disordered Pharmaceutical Materials Новинка

Marc Descamps Disordered Pharmaceutical Materials

14664.31 руб.
A one-stop resource for researchers, developers, and post graduate students in pharmaceutical science. This handbook and ready reference provides detailed, but not overloaded information – presenting the topic without unnecessarily complex formalism. As such, it gives a systematic and coherent overview of disordered materials for pharmaceutical applications, covering fundamental aspects, as well as preparation and characterization techniques for the target-oriented development of drug delivery systems based on disordered crystals and amorphous solids. Special attention is paid to examine the different facets and levels of disorder in their structural and dynamic aspects as well as the effect of disorder on dissolution and stability. Chapters on processing induced disorder and on patenting issues round off the book. As a result the book helps overcoming the challenges of using these materials in the pharmaceutical industry. For pharmaceutical and medicinal chemists, materials scientists, clinical physicists, and pharmaceutical laboratories looking to make better and more potent pharmaceuticals.
Neelottama Kushwaha, Swatantra K. S. Kushwaha Synthesis of Some Amide Derivatives and Their Biological Activity Neelottama Kushwaha, Swatantra K. S. Kushwaha Synthesis of Some Amide Derivatives and Their Biological Activity Новинка

Neelottama Kushwaha, Swatantra K. S. Kushwaha Synthesis of Some Amide Derivatives and Their Biological Activity

8639 руб.
This book has been primarily design for the undergraduate, postgraduate and researchers in pharmaceutical chemistry. In a broader perspective, the students studying pharmaceutical sciences at undergraduate, postgraduate or researchers shall be grossly benefited by it's well planned, systematically developed, structured, illustrated, expanded and elaborated subject matter. It contains all the basic concepts and principles that a researcher should know about the different aspects of the synthesis including the biological activity of the pharmaceutical compounds. This book also provides spectral analysis of newly synthesize compounds. The book is well illustrated. Hopefully it will serve as a key to the undergraduate, postgraduate and researchers in pharmaceutical chemistry.The authors earnestly believe that the wide coverage various synthetic schemes would certainly render pharmaceutical chemistry to serve as an exclusive source of information's, ideas, inspiration towards research and finding newer possible practical solutions to problems encountered in the synthesis of pharmaceutical compounds.
экодакс крем 1% 10 г экодакс крем 1% 10 г Новинка
лотосоник 20 табл лотосоник 20 табл Новинка
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.381 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.381 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.381

742 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.376 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.376 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.376

742 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.383 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.383 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 32 n.383

738 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.329 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.329 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.329

738 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.335 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.335 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.335

741 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.319 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.319 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.319

691 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.321 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.321 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 27 n.321

738 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.354 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.354 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.354

738 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 29 n.344 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 29 n.344 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 29 n.344

744 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.326 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.326 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 28 n.326

736 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.350 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.350 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 30 n.350

741 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.386 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.386 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.386

741 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.
Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.388 Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.388 Новинка

Associated Pharmaceutical Organizations of Australia The Australasian journal of pharmacy. 33 n.388

739 руб.
Эта книга — репринт оригинального издания (издательство "[Melbourne Australasian Pharmaceutical Pub. Co.]", 1885 год), созданный на основе электронной копии высокого разрешения, которую очистили и обработали вручную, сохранив структуру и орфографию оригинального издания. Редкие, забытые и малоизвестные книги, изданные с петровских времен до наших дней, вновь доступны в виде печатных книг.

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A comprehensive introduction for scientists engaged in new drug development, analysis, and approvals Each year the pharmaceutical industry worldwide recruits thousands of recent science graduates—especially chemistry, analytical chemistry, pharmacy, and pharmaceutical majors—into its ranks. However, because of their limited background in pharmaceutical analysis most of those new recruits find making the transition from academia to industry very difficult. Designed to assist both recent graduates, as well as experienced chemists or scientists with limited regulatory, compendial or pharmaceutical analysis background, make that transition, Pharmaceutical Analysis for Small Molecules is a concise, yet comprehensive introduction to the drug development process and analysis of chemically synthesized, small molecule drugs. It features contributions by distinguished experts in the field, including editor and author, Dr. Behnam Davani, an analytical chemist with decades of technical management and teaching experience in compendial, regulatory, and industry. This book provides an introduction to pharmaceutical analysis for small molecules (non-biologics) using commonly used techniques for drug characterization and performance tests. The driving force for industry to perform pharmaceutical analyses is submission of such data and supporting documents to regulatory bodies for drug approval in order to market their products. In addition, related required supporting studies including good laboratory/documentation practices including analytical instrument qualification are highlighted in this book. Topics covered include: Drug Approval Process and Regulatory Requirements (private standards) Pharmacopeias and Compendial Approval Process (public standards) Common methods in pharmaceutical analysis (typically compendial) Common Calculations for assays and impurities and other specific tests Analytical Method Validation, Verification, Transfer Specifications including how to handle out of specification (OOS) and out of trend (OOT) Impurities including organic, inorganic, residual solvents and elemental impurities Good Documentation Practices for regulatory environment Management of Analytical Laboratories Analytical Instrument Qualifications including IQ, OQ, PQ and VQ Due to global nature of pharmaceutical industry, other topics on both regulatory (ICH) and Compendial harmonization are also highlighted. Pharmaceutical Analysis for Small Molecules is a valuable working resource for scientists directly or indirectly involved with the drug development process, including analytical chemists, pharmaceutical scientists, pharmacists, and quality control/quality assurance professionals. It also is an excellent text/reference for graduate students in analytical chemistry, pharmacy, pharmaceutical and regulatory sciences.
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