Dietary Supplement and Nonprescription Drug Consumer Protection Act (P.L. 109-462) PDF Download

Author: Donna Viola Porter
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 6

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Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 32

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Author: United States. Congress. Senate
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
ISBN:
Category : Consumer protection
Languages : en
Pages : 26

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Author: National Research Council
Publisher: National Academies Press
ISBN: 0309163587
Category : Medical
Languages : en
Pages : 589

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Book Description
Recent outbreaks of illnesses traced to contaminated sprouts and lettuce illustrate the holes that exist in the system for monitoring problems and preventing foodborne diseases. Although it is not solely responsible for ensuring the safety of the nation's food supply, the U.S. Food and Drug Administration (FDA) oversees monitoring and intervention for 80 percent of the food supply. The U.S. Food and Drug Administration's abilities to discover potential threats to food safety and prevent outbreaks of foodborne illness are hampered by impediments to efficient use of its limited resources and a piecemeal approach to gathering and using information on risks. Enhancing Food Safety: The Role of the Food and Drug Administration, a new book from the Institute of Medicine and the National Research Council, responds to a congressional request for recommendations on how to close gaps in FDA's food safety systems. Enhancing Food Safety begins with a brief review of the Food Protection Plan (FPP), FDA's food safety philosophy developed in 2007. The lack of sufficient detail and specific strategies in the FPP renders it ineffectual. The book stresses the need for FPP to evolve and be supported by the type of strategic planning described in these pages. It also explores the development and implementation of a stronger, more effective food safety system built on a risk-based approach to food safety management. Conclusions and recommendations include adopting a risk-based decision-making approach to food safety; creating a data surveillance and research infrastructure; integrating federal, state, and local government food safety programs; enhancing efficiency of inspections; and more. Although food safety is the responsibility of everyone, from producers to consumers, the FDA and other regulatory agencies have an essential role. In many instances, the FDA must carry out this responsibility against a backdrop of multiple stakeholder interests, inadequate resources, and competing priorities. Of interest to the food production industry, consumer advocacy groups, health care professionals, and others, Enhancing Food Safety provides the FDA and Congress with a course of action that will enable the agency to become more efficient and effective in carrying out its food safety mission in a rapidly changing world.

Author: United States
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 1274

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"The United States Code is the official codification of the general and permanent laws of the United States of America. The Code was first published in 1926, and a new edition of the code has been published every six years since 1934. The 2012 edition of the Code incorporates laws enacted through the One Hundred Twelfth Congress, Second Session, the last of which was signed by the President on January 15, 2013. It does not include laws of the One Hundred Thirteenth Congress, First Session, enacted between January 2, 2013, the date it convened, and January 15, 2013. By statutory authority this edition may be cited "U.S.C. 2012 ed." As adopted in 1926, the Code established prima facie the general and permanent laws of the United States. The underlying statutes reprinted in the Code remained in effect and controlled over the Code in case of any discrepancy. In 1947, Congress began enacting individual titles of the Code into positive law. When a title is enacted into positive law, the underlying statutes are repealed and the title then becomes legal evidence of the law. Currently, 26 of the 51 titles in the Code have been so enacted. These are identified in the table of titles near the beginning of each volume. The Law Revision Counsel of the House of Representatives continues to prepare legislation pursuant to 2 U.S.C. 285b to enact the remainder of the Code, on a title-by-title basis, into positive law. The 2012 edition of the Code was prepared and published under the supervision of Ralph V. Seep, Law Revision Counsel. Grateful acknowledgment is made of the contributions by all who helped in this work, particularly the staffs of the Office of the Law Revision Counsel and the Government Printing Office"--Preface.

Author: Richard R. Abood
Publisher: Jones & Bartlett Publishers
ISBN: 1449686915
Category : Law
Languages : en
Pages : 497

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The Seventh Edition of this best-selling text includes updates to account for new legal, regulatory, and policy developments. Pharmacy Practice and the Law, Seventh Edition provides background, history, and discussion of the law to The Seventh Edition of this best-selling text includes updates to account for new legal, regulatory, and policy developments. Pharmacy Practice and the Law, Seventh Edition provides background, history, and discussion of the law to enable students not only to learn the facts, but to help them understand, apply, and critically evaluate the information and how it will affect their practice. Challenging open-ended discussion questions and edited cases are included in every chapter to facilitate discussion and critical thinking. Citations to all laws, court cases, regulations, and other documents are provided. Critical issues are discussed in non-legal, easy-to-understand language, and the newest edition features an accessible and engaging new, colorful layout to better highlight the important content as well as online support for better reader comprehension. Pharmacy Practice and the Law, Seventh Edition is the essential resource both for teaching the facts of pharmacy law and for stimulating critical thinking issues in pharmacy law. The Seventh Edition of this best-selling text includes updates to account for new legal, regulatory, and policy developments. Pharmacy Practice and the Law, Seventh Edition provides background, history, and discussion of the law to enable students not only to learn the facts, but to help them understand, apply, and critically evaluate the information and how it will affect their practice. Pharmacy Practice and the Law, Seventh Edition is the essential resource both for teaching the facts of pharmacy law and for stimulating critical thinking issues in pharmacy law. Features * Challenging open-ended discussion questions * Edited cases in each chapter * Citations and documentation for all laws, court cases, and regulations * Non-legal, easy-to-understand language is used to discuss critical issues * Accessible and engaging new, colorful layout * Online interactive activities to aid and enhance reader comprehension Instructor Resources: Case Studies, Instructor's Manual, PowerPoint Presentations, Test Bank Student Resources: Companion Website including: Case Studies, Crossword Puzzles, Interactive Flashcards, Interactive Glossary, Matching Exercises Each new printed textbook copy of Pharmacy Practice and the Law, Seventh Edition includes an access code card with login information for the accompanying Student Companion Website. For more information on the Companion Website or to purchase individual access click here. Available February 2013.

Author: Taylor C. Wallace
Publisher: Springer Science & Business Media
ISBN: 3319015028
Category : Science
Languages : en
Pages : 51

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Contrary to the common belief that dietary supplements are “unregulated” in the United States, nutrients and other dietary ingredient-containing products have been regulated in this country for a little over a century at least in some capacity, initially through the Pure Food and Drug Act (PFDA) of 1906 and culminating with the many anticipated regulations to be implemented following the recent enactment of the Food Safety Modernization Act of 2010 (FSMA). The goal of this brief is to review and discuss the current statutes and regulations surrounding the ingredients, manufacturing standards, safety, and labeling of dietary supplements for the purpose of protecting consumers. ​

Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309116171
Category : Technology & Engineering
Languages : en
Pages : 474

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Dietary supplements are widely available through a rapidly expanding market of products commonly advertised as beneficial for health, performance enhancement, and disease prevention. Given the importance and frequent evaluation of physical performance and health as a criteria to join and remain in the military, the use of these products by military personnel has raised concern regarding over-all and long-term efficacy and safety. This evaluation is especially difficult, as many of these supplements contain multiple ingredients, have a changing composition over time, or are used intermittently at doses difficult to measure. This book analyzes the patterns of dietary supplement use among military personnel, examines published reviews of the scientific evidence, and identifies those dietary supplements that are beneficial and/or warrant concern due to risks to health or performance. The book also recommends a system to monitor adverse health effects and a framework to identify the need for active management of dietary supplements by military personnel. Military policy makers, personnel, and recruits will find this book useful, as will nutritionists, athletes, and others working in strenuous environments.