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Appraisal Of The Safety Of Chemicals In Foods Drugs And Cosmetics
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Book Synopsis Appraisal of the Safety of Chemicals in Foods, Drugs, and Cosmetics by : United States. Food and Drug Administration
Download or read book Appraisal of the Safety of Chemicals in Foods, Drugs, and Cosmetics written by United States. Food and Drug Administration and published by . This book was released on 1959 with total page 124 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics by : Association of Food and Drug Officials of the United States
Download or read book Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics written by Association of Food and Drug Officials of the United States and published by . This book was released on 1979 with total page 107 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Principles and Methods of Toxicology, Fifth Edition by : A. Wallace Hayes
Download or read book Principles and Methods of Toxicology, Fifth Edition written by A. Wallace Hayes and published by CRC Press. This book was released on 2007-09-25 with total page 2304 pages. Available in PDF, EPUB and Kindle. Book excerpt: Founded on the paradox that all things are poisons and the difference between poison and remedy is quantity, the determination of safe dosage forms the base and focus of modern toxicology. In order to make a sound determination there must be a working knowledge of the biologic mechanisms involved and of the methods employed to define these mechanisms. While the vastness of the field and the rapid accumulation of data may preclude the possibility of absorbing and retaining more than a fraction of the available information, a solid understanding of the underlying principles is essential. Extensively revised and updated with four new chapters and an expanded glossary, this fifth edition of the classic text, Principles and Methods of Toxicology provides comprehensive coverage in a manageable and accessible format. New topics include 'toxicopanomics', plant and animal poisons, information resources, and non-animal testing alternatives. Emphasizing the cornerstones of toxicology-people differ, dose matters, and things change, the book begins with a review of the history of toxicology and followed by an explanation of basic toxicological principles, agents that cause toxicity, target organ toxicity, and toxicological testing methods including many of the test protocols required to meet regulatory needs worldwide. The book examines each method or procedure from the standpoint of technique and interpretation of data and discusses problems and pitfalls that may be associated with each. The addition of several new authors allow for a broader and more diverse treatment of the ever-changing and expanding field of toxicology. Maintaining the high-quality information and organizational framework that made the previous editions so successful, Principles and Methods of Toxicology, Fifth Edition continues to be a valuable resource for the advanced practitioner as well as the new disciple of toxicology.
Book Synopsis Handbook of Toxicology, Second Edition by : Michael J. Derelanko
Download or read book Handbook of Toxicology, Second Edition written by Michael J. Derelanko and published by CRC Press. This book was released on 2001-08-29 with total page 1448 pages. Available in PDF, EPUB and Kindle. Book excerpt: LOCATE FREQUENTLY USED INFORMATION EASILY AND QUICKLY Working in the laboratory or office, you use a diverse assortment of basic information to design, conduct, and interpret toxicology studies and to perform risk assessments. The Second Edition of the best-selling Handbook of Toxicology gives you the information you need in a single reference source. NEW IN THIS EDITION: Expanded coverage of inhalation toxicology, neurotoxicology, and histopathology Additional regulatory chapters dealing with pesticides, medical devices, consumer products, and world-wide notification of new chemicals Areas of toxicology missing from the first edition such as ecotoxicology and in vitro toxicology A chapter providing extensive overview of the toxicology of metals Two chapters on basic male and female endocrinology and related toxicology Information on differences in physiological and biochemical parameters between children and adults References to Web site sources of valuable information Over 200 new tables and figures THE SINGLE SOURCE FOR THE INFORMATION YOU USE MOST FREQUENTLY Updated and expanded, this unique book includes practical reference information useful to toxicologists in the chemical and pharmaceutical industries, contract laboratories, regulatory agencies, and academia. To help you find information quickly and easily, data is arranged by toxicology subspecialty and each chapter begins with a detailed listing of information presented. Containing over 700 tables and figures, Handbook of Toxicology, Second Edition gives you a single source for the information you use most often.
Book Synopsis Safety Evaluation of Drugs & Chemicals by : W. Eugene Lloyd
Download or read book Safety Evaluation of Drugs & Chemicals written by W. Eugene Lloyd and published by CRC Press. This book was released on 1986-02-01 with total page 512 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Handbook of Occupational Dermatology by : Lasse Kanerva
Download or read book Handbook of Occupational Dermatology written by Lasse Kanerva and published by Springer Science & Business Media. This book was released on 2000 with total page 1330 pages. Available in PDF, EPUB and Kindle. Book excerpt: This text combines a highly practical approach to the occupational dermatoses with the skill and experience of scientists who have specialized in this area of clinical and experimental dermatology. The spectrum of diseases covered includes allergic and irritant dermatitis, contact urticaria, photodermatoses, systemic reactions due to percutaneous absorption, infectious diseases and skin tumors. Furthermore, diseases predisposing to occupational skin problems such as atopic dermatitis and psoriasis are discussed. This book provides badly needed information for daily patient management and presents precise job descriptions and algorithms how to optimize the diagnostic procedure for high quality patient care and expert opinion in occupational dermatology.
Book Synopsis A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments by :
Download or read book A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments written by and published by . This book was released on 1979 with total page 840 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments by : United States
Download or read book A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments written by United States and published by . This book was released on 1979 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Explores how the human brain works, covering such topics as memory, sleep, dreaming, dysfunctions, and new technology used to learn more about it.
Book Synopsis A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments by : United States
Download or read book A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its Amendments written by United States and published by . This book was released on 1979 with total page 1566 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author :United States. Congress. House. Committee on Government Operations Publisher : ISBN 13 : Total Pages :368 pages Book Rating :4.3/5 (91 download)
Book Synopsis Drug Safety by : United States. Congress. House. Committee on Government Operations
Download or read book Drug Safety written by United States. Congress. House. Committee on Government Operations and published by . This book was released on 1964 with total page 368 pages. Available in PDF, EPUB and Kindle. Book excerpt: Hearings held Mar. 9, 10, May 25, 26, June 7-9, 1966--pt.5.
Author :United States. Congress. House. Committee on Government Operations. Intergovernmental Relations Subcommittee Publisher : ISBN 13 : Total Pages :2438 pages Book Rating :4.:/5 (319 download)
Book Synopsis Drug Safety by : United States. Congress. House. Committee on Government Operations. Intergovernmental Relations Subcommittee
Download or read book Drug Safety written by United States. Congress. House. Committee on Government Operations. Intergovernmental Relations Subcommittee and published by . This book was released on 1964 with total page 2438 pages. Available in PDF, EPUB and Kindle. Book excerpt: Hearings held Mar. 9, 10, May 25, 26, June 7-9, 1966--pt. 5.
Download or read book Federal Register written by and published by . This book was released on 1979-07 with total page 2204 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis The Contribution of Acute Toxicity Testing to the Evaluation of Pharmaceuticals by : Dietrich Schuppan
Download or read book The Contribution of Acute Toxicity Testing to the Evaluation of Pharmaceuticals written by Dietrich Schuppan and published by Springer. This book was released on 2014-11-14 with total page 110 pages. Available in PDF, EPUB and Kindle. Book excerpt: International Symposium. IFPMA Symposium, Geneva 30-31 October 1984
Book Synopsis Reputation and Power by : Daniel Carpenter
Download or read book Reputation and Power written by Daniel Carpenter and published by Princeton University Press. This book was released on 2014-04-24 with total page 856 pages. Available in PDF, EPUB and Kindle. Book excerpt: How the FDA became the world's most powerful regulatory agency The U.S. Food and Drug Administration is the most powerful regulatory agency in the world. How did the FDA become so influential? And how exactly does it wield its extraordinary power? Reputation and Power traces the history of FDA regulation of pharmaceuticals, revealing how the agency's organizational reputation has been the primary source of its power, yet also one of its ultimate constraints. Daniel Carpenter describes how the FDA cultivated a reputation for competence and vigilance throughout the last century, and how this organizational image has enabled the agency to regulate an industry as powerful as American pharmaceuticals while resisting efforts to curb its own authority. Carpenter explains how the FDA's reputation and power have played out among committees in Congress, and with drug companies, advocacy groups, the media, research hospitals and universities, and governments in Europe and India. He shows how FDA regulatory power has influenced the way that business, medicine, and science are conducted in the United States and worldwide. Along the way, Carpenter offers new insights into the therapeutic revolution of the 1940s and 1950s; the 1980s AIDS crisis; the advent of oral contraceptives and cancer chemotherapy; the rise of antiregulatory conservatism; and the FDA's waning influence in drug regulation today. Reputation and Power demonstrates how reputation shapes the power and behavior of government agencies, and sheds new light on how that power is used and contested. Some images inside the book are unavailable due to digital copyright restrictions.
Book Synopsis Comprehensive Medicinal Chemistry III by :
Download or read book Comprehensive Medicinal Chemistry III written by and published by Elsevier. This book was released on 2017-06-03 with total page 4609 pages. Available in PDF, EPUB and Kindle. Book excerpt: Comprehensive Medicinal Chemistry III, Eight Volume Set provides a contemporary and forward-looking critical analysis and summary of recent developments, emerging trends, and recently identified new areas where medicinal chemistry is having an impact. The discipline of medicinal chemistry continues to evolve as it adapts to new opportunities and strives to solve new challenges. These include drug targeting, biomolecular therapeutics, development of chemical biology tools, data collection and analysis, in silico models as predictors for biological properties, identification and validation of new targets, approaches to quantify target engagement, new methods for synthesis of drug candidates such as green chemistry, development of novel scaffolds for drug discovery, and the role of regulatory agencies in drug discovery. Reviews the strategies, technologies, principles, and applications of modern medicinal chemistry Provides a global and current perspective of today's drug discovery process and discusses the major therapeutic classes and targets Includes a unique collection of case studies and personal assays reviewing the discovery and development of key drugs
Book Synopsis Food Protection Technology by : Charles W. Felix
Download or read book Food Protection Technology written by Charles W. Felix and published by CRC Press. This book was released on 2018-01-18 with total page 438 pages. Available in PDF, EPUB and Kindle. Book excerpt: A reference text for US federal, state, and local environmental health officials concerned with food safety and for their US food industry counterparts presents the proceedings of the 1986 Conference for Food Protection. The text includes 36 technical papers grouped among 6 specific areasof food safety, viz.: toxicology; microbiology; good manufacturing practice regulations and guidelines, including quality control and quality assurance concepts; consumer education on food and nutrition; and the processing and packaging of new foods and new processing technologies (e.g.: genetic engineering, food-packaging interactions, irradiation processing, aseptic packaging, biotechnology). Specific recommendations by committees representing each of these 6 areas are included
Book Synopsis Risk Assessment in the Federal Government by : National Research Council
Download or read book Risk Assessment in the Federal Government written by National Research Council and published by National Academies Press. This book was released on 1983-02-01 with total page 206 pages. Available in PDF, EPUB and Kindle. Book excerpt: The regulation of potentially hazardous substances has become a controversial issue. This volume evaluates past efforts to develop and use risk assessment guidelines, reviews the experience of regulatory agencies with different administrative arrangements for risk assessment, and evaluates various proposals to modify procedures. The book's conclusions and recommendations can be applied across the entire field of environmental health.
