Regulatory Toxicology, Third Edition
eBook - ePub

Regulatory Toxicology, Third Edition

  1. 354 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Regulatory Toxicology, Third Edition

About this book

This practical book provides toxicologists with essential information on the regulations that govern their jobs and products. Regulatory Toxicology, Third Edition is an up-to-date guide to required safety assessment for the entire range of man-made marketed products. Individual chapters written by experts with extensive experience in the field address requirements not only for human pharmaceuticals and medical devices (for which there are available guidances), but for the full range of man-made products. New in this edition are three chapters addressing Safety Data Sheet Preparation, Regulatory Requirements for GMOs, and Regulatory Requirements for Tobacco and Marijuana. The major administrative divisions for regulatory agencies and their main responsibilities are also detailed, as are the basic filing documents the agencies require.

Coverage includes food additives, dietary supplements, cosmetics, over-the-counter drugs, personal care and consumer products, agriculture and GMO products, industrial chemicals, air and drinking water regulations and the special cases of California's Proposition 65, requirements for safety data sheets, and oversight regulations. Both US and international requirements are clearly presented and referenced. In one volume, those who have regulatory responsibility in companies, lawyers, educators, and those selling these materials in the marketplace can learn about regulatory requirements and how to meet them.

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Yes, you can access Regulatory Toxicology, Third Edition by Shayne C. Gad in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmacology. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2018
Print ISBN
9781498780827
eBook ISBN
9780429876516
Edition
3
Topic
Medicine
Subtopic
Pharmacology

Table of contents

  1. Cover
  2. Half Title
  3. Title Page
  4. Copyright Page
  5. Table of Contents
  6. Preface
  7. Editor
  8. Contributors
  9. Chapter 1 Introduction
  10. Chapter 2 Human Pharmaceutical Product Safety
  11. Chapter 3 Animal Health Products
  12. Chapter 4 Regulatory Aspects and Strategy in Medical Device and Biomaterials Safety Evaluation
  13. Chapter 5 Food Additives and Nutrition Supplements
  14. Chapter 6 Regulations Affecting Cosmetic and Personal Care Products
  15. Chapter 7 OTC Drugs and Nutraceuticals
  16. Chapter 8 Consumer Products: Nonpersonal Care Products Regulatory Review and Labeling
  17. Chapter 9 Agricultural Chemicals: Regulation, Risk Assessment, and Risk Management
  18. Chapter 10 Industrial Chemicals Regulation of New and Existing Chemicals (The Toxic Substances Control Act and Similar Worldwide Chemical Control Laws)
  19. Chapter 11 Industrial Chemicals: Hazard Communication, Exposure Limits, Labeling and Other Workplace and Transportation Requirements under Occupational Safety and Health Administration, Department of Transportation, and Similar Authorities around the World
  20. Chapter 12 Federal Air and Water Regulations: Clean Air Act, Clean Water Act, and Safe Drinking Water Act
  21. Chapter 13 Understanding the Safe Drinking Water and Toxic Enforcement Act of 1986 (California’s Proposition 65)
  22. Chapter 14 Safety Data Sheets
  23. Chapter 15 Genetically Modified Organisms—Evolution or Revolution of Genetics: Assessing the Health Risks of Foods and Crops
  24. Chapter 16 Oversight Regulations
  25. Appendix I: Selected Regulatory and Toxicological Acronyms
  26. Appendix II
  27. Index