An Act to Amend the Federal Food, Drug, and Cosmetic Act to Clarify the Application of the Act with Respect to Alternate Uses of New Animal Drugs and New Drugs Intended for Human Use, and for Other Purposes PDF Download
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Author: United States
Publisher:
ISBN:
Category : Animal extracts
Languages : en
Pages : 3
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Book Description
Author: United States
Publisher:
ISBN:
Category : Animal extracts
Languages : en
Pages : 3
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Book Description
Author: National Research Council
Publisher: National Academies Press
ISBN: 0309175771
Category : Medical
Languages : en
Pages : 276
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Book Description
The use of drugs in food animal production has resulted in benefits throughout the food industry; however, their use has also raised public health safety concerns. The Use of Drugs in Food Animals provides an overview of why and how drugs are used in the major food-producing animal industriesâ€"poultry, dairy, beef, swine, and aquaculture. The volume discusses the prevalence of human pathogens in foods of animal origin. It also addresses the transfer of resistance in animal microbes to human pathogens and the resulting risk of human disease. The committee offers analysis and insight into these areas: Monitoring of drug residues. The book provides a brief overview of how the FDA and USDA monitor drug residues in foods of animal origin and describes quality assurance programs initiated by the poultry, dairy, beef, and swine industries. Antibiotic resistance. The committee reports what is known about this controversial problem and its potential effect on human health. The volume also looks at how drug use may be minimized with new approaches in genetics, nutrition, and animal management.
Author: United States
Publisher:
ISBN:
Category : Animals
Languages : en
Pages : 10
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Author: United States
Publisher:
ISBN:
Category : Animal health
Languages : en
Pages : 21
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Book Description
Author: United States. Congress. House. Interstate and Foreign Commerce
Publisher:
ISBN:
Category :
Languages : en
Pages : 74
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Book Description
Author: United States
Publisher: Department of Health and Human Services Public Health Service Food and Drug Administration
ISBN:
Category : Cosmetics
Languages : en
Pages : 232
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Book Description
Cover title: Federal Food, Drug, and Cosmetic Act, as amended.
Author:
Publisher:
ISBN:
Category : Cosmetics
Languages : en
Pages : 958
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Book Description
Author: United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 118
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Book Description
Considers S. 1600 and H.R. 3639, to amend the Federal Food, Drug, and Cosmetic Act to consolidate existing procedures premarketing clearance of chemicals and drugs used in veterinary medicine and medicated feeds.
Author: United States
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 88
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Book Description
Author: The Law The Law Library
Publisher: Createspace Independent Publishing Platform
ISBN: 9781727546538
Category :
Languages : en
Pages : 120
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Book Description
Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA) is amending its regulations governing drug establishment registration and drug listing. These amendments reorganize, modify, and clarify current regulations concerning who must register establishments and list human drugs, human drugs that are also biological products, and animal drugs. The final rule requires electronic submission, unless waived in certain circumstances, of registration and listing information. This rulemaking pertains to finished drug products and to active pharmaceutical ingredients (APIs) alone or together with one or more other ingredients. The final rule describes how and when owners or operators of establishments at which drugs are manufactured or processed must register their establishments with FDA and list the drugs they manufacture or process. In addition, the rule makes certain changes to the National Drug Code (NDC) system. We are taking this action to improve management of drug establishment registration and drug listing requirements and make these processes more efficient and effective for industry and for us. This action also supports implementation of the electronic prescribing provisions of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) and the availability of current drug labeling information through DailyMed, a computerized repository of drug information maintained by the National Library of Medicine. This book contains: - The complete text of the Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section
