Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 32
Book Description
Dietary Supplement and Nonprescription Drug Consumer Protection Act
Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 32
Book Description
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 32
Book Description
Dietary Supplement and Nonprescription Drug Consumer Protection Act (P.L. 109-462)
Author: Donna Viola Porter
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 6
Book Description
Publisher:
ISBN:
Category : Dietary supplements
Languages : en
Pages : 6
Book Description
Dietary Supplement and Nonprescription Drug Consumer Protection Act
Author: United States. Congress. Senate. Committee on Health, Education, Labor, and Pensions
Publisher:
ISBN:
Category : Consumer protection
Languages : en
Pages : 26
Book Description
Publisher:
ISBN:
Category : Consumer protection
Languages : en
Pages : 26
Book Description
DIETARY SUPPLEMENT AND NONPRESCRIPTION DRUG CONSUMER PROTECTION ACT, SEPTEMBER 5, 2006, 109-2 SENATE REPORT 109-324
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Dietary Supplement and Nonprescription Drug Consumer Protection Act... Report... Report 109-324... U.S. Congress, 109th Congress, 2nd Session
Author: United States. Congress. Senate
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category :
Languages : en
Pages :
Book Description
Dietary Supplements Manufacturing and Distribution
Author: Kirstin A. Counts
Publisher: PharmaLogika Books
ISBN: 9781937258191
Category :
Languages : en
Pages : 756
Book Description
Dietary Supplements Manufacturing and Distribution is a unified reference source for the U.S. Food and Drug Administration's regulations, guidance, and associated documents pertaining to the manufacture and distribution of dietary supplements. The dietary supplement industry includes a vast array of ingredients, product forms, suppliers, manufacturers, and distributors. With such diversity in the marketplace it is important to fully understand the rules governing the industry. It is the responsibility of the participants in all stages of the manufacturing and distribution process to protect dietary supplement consumers and to provide safe and consistent products. This reference book is a compilation of 21CFR (Code of Federal Regulations, Title 21) as it applies to dietary supplements, DSHEA (Dietary Supplements Health and Education Act of 1994), DSNDCPA (Dietary Supplement and Nonprescription Drug Consumer Protection Act), and related guidance documents. Also included are selected warning letters demonstrating communications from the FDA, a combined glossary of the legally defined terms, and a detailed index. Included Documents and Features: - FDA Overview and Orientation - Introduction to Dietary Supplements - Part 1: General Enforcement Regulations - Part 101: Food Labeling - Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements - Part 119: Dietary Supplements that Present a Significant or Unreasonable Risk - Part 190: Dietary Supplements - Dietary Supplement and Nonprescription Drug Consumer Protection Act - Dietary Supplement Health and Education Act of 1994 - Guidance Documents - Sample Warning Letters - Combined Glossary and Index
Publisher: PharmaLogika Books
ISBN: 9781937258191
Category :
Languages : en
Pages : 756
Book Description
Dietary Supplements Manufacturing and Distribution is a unified reference source for the U.S. Food and Drug Administration's regulations, guidance, and associated documents pertaining to the manufacture and distribution of dietary supplements. The dietary supplement industry includes a vast array of ingredients, product forms, suppliers, manufacturers, and distributors. With such diversity in the marketplace it is important to fully understand the rules governing the industry. It is the responsibility of the participants in all stages of the manufacturing and distribution process to protect dietary supplement consumers and to provide safe and consistent products. This reference book is a compilation of 21CFR (Code of Federal Regulations, Title 21) as it applies to dietary supplements, DSHEA (Dietary Supplements Health and Education Act of 1994), DSNDCPA (Dietary Supplement and Nonprescription Drug Consumer Protection Act), and related guidance documents. Also included are selected warning letters demonstrating communications from the FDA, a combined glossary of the legally defined terms, and a detailed index. Included Documents and Features: - FDA Overview and Orientation - Introduction to Dietary Supplements - Part 1: General Enforcement Regulations - Part 101: Food Labeling - Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements - Part 119: Dietary Supplements that Present a Significant or Unreasonable Risk - Part 190: Dietary Supplements - Dietary Supplement and Nonprescription Drug Consumer Protection Act - Dietary Supplement Health and Education Act of 1994 - Guidance Documents - Sample Warning Letters - Combined Glossary and Index
Dietary Supplements
Author: United States. Federal Trade Commission. Bureau of Consumer Protection
Publisher:
ISBN:
Category : Advertising
Languages : en
Pages : 32
Book Description
Publisher:
ISBN:
Category : Advertising
Languages : en
Pages : 32
Book Description
Dietary Supplements
Author: Mindy J. Allport-Settle
Publisher: Pharmalogika
ISBN: 9780983071921
Category : Law
Languages : en
Pages : 428
Book Description
This book is designed to be a unified reference source for the U.S. Food and Drug Adminstration's Dietary Supplements regulations, guidance, and associated documents. Dietary Supplements Regulations and Guidance: * FDA Overview and Orientation * Introduction to Dietary Supplements * Part I: Regulations - Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements - Part 101: Food Labeling - Part 190: Diettary Supplements * Part II: Legislative Acts and Significant Amendments - Dietary Supplement and Nonprescription Drug Consumer Protection Act - Dietary Supplement Health and Education Act of 1994 * Part III: Guidance and Associated Documents - Dietary Supplements Final Rule - Dietary Supplement Current Good Manufacturing Practices (CGMPs) and Interim Final Rule (IFR) Facts - Dietary Supplement Labeling Guide - Structure/Function Claims, Small Entity Compliance Guide - Notification of a Health Claim or Nutrient Content Claim Based on an Authoritative Statement of a Scientific Body - Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act - Responses to Questions about Codex and Dietary Supplements Reference Tools * Part IV: Combined Glossary and Index
Publisher: Pharmalogika
ISBN: 9780983071921
Category : Law
Languages : en
Pages : 428
Book Description
This book is designed to be a unified reference source for the U.S. Food and Drug Adminstration's Dietary Supplements regulations, guidance, and associated documents. Dietary Supplements Regulations and Guidance: * FDA Overview and Orientation * Introduction to Dietary Supplements * Part I: Regulations - Part 111: Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements - Part 101: Food Labeling - Part 190: Diettary Supplements * Part II: Legislative Acts and Significant Amendments - Dietary Supplement and Nonprescription Drug Consumer Protection Act - Dietary Supplement Health and Education Act of 1994 * Part III: Guidance and Associated Documents - Dietary Supplements Final Rule - Dietary Supplement Current Good Manufacturing Practices (CGMPs) and Interim Final Rule (IFR) Facts - Dietary Supplement Labeling Guide - Structure/Function Claims, Small Entity Compliance Guide - Notification of a Health Claim or Nutrient Content Claim Based on an Authoritative Statement of a Scientific Body - Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act - Responses to Questions about Codex and Dietary Supplements Reference Tools * Part IV: Combined Glossary and Index
Dietary Supplement Safety Act
Author: United States. Congress. Senate. Committee on Governmental Affairs. Subcommittee on Oversight of Government Management, the Federal Workforce, and the District of Columbia
Publisher:
ISBN:
Category : Health & Fitness
Languages : en
Pages : 144
Book Description
Publisher:
ISBN:
Category : Health & Fitness
Languages : en
Pages : 144
Book Description
Dietary Supplement Regulation in the United States
Author: Taylor C. Wallace
Publisher: Springer Science & Business Media
ISBN: 3319015028
Category : Science
Languages : en
Pages : 51
Book Description
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.
Publisher: Springer Science & Business Media
ISBN: 3319015028
Category : Science
Languages : en
Pages : 51
Book Description
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.