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Author : Anonim
Publisher : Unknown
Page : 840 pages
File Size : 40,5 Mb
Release : 1979
Category : Cosmetics
ISBN : UOM:39015022630142
Author : United States
Publisher : Unknown
Page : 128 pages
File Size : 45,8 Mb
Release : 1979
Category : Cosmetics
ISBN : OCLC:5929678
Author : Anonim
Publisher : Unknown
Page : 128 pages
File Size : 45,8 Mb
Release : 1979
Category : Cosmetics
ISBN : OCLC:5929678
Author : United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Public Health and Environment
Publisher : Unknown
Page : 32 pages
File Size : 51,5 Mb
Release : 1974
Category : Electronic
ISBN : UOM:39015078683052
Author : Charles Wesley Dunn
Publisher : Unknown
Page : 1448 pages
File Size : 46,9 Mb
Release : 1987
Category : Cosmetics
ISBN : MINN:319510026735987
Author : Anonim
Publisher : Unknown
Page : 826 pages
File Size : 42,5 Mb
Release : 1979
Category : Cosmetics
ISBN : UOM:39015022629979
Author : National Research Council,Board on Agriculture,Committee on Scientific and Regulatory Issues Underlying Pesticide Use Patterns and Agricultural Innovation
Publisher : National Academies Press
Page : 288 pages
File Size : 53,5 Mb
Release : 1987-02-01
Category : Medical
ISBN : 9780309037464
Concern about health effects from exposure to pesticides in foods is growing as scientists learn more about the toxic properties of pesticides. The Delaney Clause, a provision of the Food, Drug and Cosmetic Act, prohibits tolerances for any pesticide that causes cancer in test animals or in humans if the pesticide concentrates in processed food or feeds. This volume examines the impacts of the Delaney Clause on agricultural innovation and on the public's dietary exposure to potentially carcinogenic pesticide residues. Four regulatory scenarios are described to illustrate the effects of varying approaches to managing oncogenic pesticide residues in food.
Author : United States
Publisher : Unknown
Page : 400 pages
File Size : 52,9 Mb
Release : 1989
Category : Cosmetics
ISBN : 1885259069
Author : United States. Congress. Senate. Committee on Commerce
Publisher : Unknown
Page : 520 pages
File Size : 48,5 Mb
Release : 1934
Category : Cosmetics industry
ISBN : MINN:31951D02156318D
Considers legislation to prevent sale and false advertising of adulterated and misbranded food, drugs, and cosmetics.
Author : Institute of Medicine,Food Forum
Publisher : National Academies Press
Page : 158 pages
File Size : 52,9 Mb
Release : 1999-04-29
Category : Medical
ISBN : 9780309184137
The Institute of Medicine's (IOM's) Food Forum was established in 1993 to allow science and technology leaders in the food industry, top administrators in the federal government, representatives from consumer interest groups, and academicians to discuss and debate food and food safety issues openly and in a neutral setting. The Forum provides a mechanism for these diverse groups to identify possible approaches for addressing food and food safety problems and issues surrounding the often complex interactions among industry, academia, regulatory agencies, and consumers. On May 6-7, 1997, the Forum convened a workshop titled Enhancing the Regulatory Decision-Making Process for Direct Food Ingredient Technologies. Workshop speakers and participants discussed legal aspects of the direct food additive approval process, changes in science and technology, and opportunities for reform. Two background papers, which can be found in Appendix A and B, were shared with the participants prior to the workshop. The first paper provided a description and history of the legal framework of the food ingredient approval process and the second paper focused on changes in science and technology practices with emphasis placed on lessons learned from case studies. This document presents a summary of the workshop.
Author : United States Government Printing Office
Publisher : Unknown
Page : 250 pages
File Size : 43,9 Mb
Release : 1990-03
Category : Electronic
ISBN : 0160187885
Author : Institute of Medicine,Board on Population Health and Public Health Practice,Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
Publisher : National Academies Press
Page : 141 pages
File Size : 52,6 Mb
Release : 2010-10-04
Category : Medical
ISBN : 9780309162906
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.
Author : Committee on Federal Regulation of Methadone Treatment,Institute of Medicine
Publisher : National Academies Press
Page : 223 pages
File Size : 52,7 Mb
Release : 1995-02-01
Category : Medical
ISBN : 9780309598620
For nearly three decades, methadone hydrochloride has been the primary means of treating opiate addiction. Today, about 115,000 people receive such treatment, and thousands more have benefited from it in the past. Even though methadone's effectiveness has been well established, its use remains controversial, a fact reflected by the extensive regulation of its manufacturing, labeling, distribution, and use. The Food and Drug Administration regulates the safety and effectiveness of methadone, as it does for all drugs, and the Drug Enforcement Administration regulates it as a controlled substance. However, methadone is also subjected to a unique additional tier of regulation that prescribes how and under what circumstances it may be used to treat opiate addiction. Federal Regulation of Methadone Treatment examines current Department of Health and Human Services standards for narcotic addiction treatment and the regulation of methadone treatment programs pursuant to those standards. The book includes an evaluation of the effect of federal regulations on the provision of methadone treatment services and an exploration of options for modifying the regulations to allow optimal clinical practice. The volume also includes an assessment of alternatives to the existing regulations.
Author : Institute of Medicine,Board on Population Health and Public Health Practice,Committee on the Public Health Effectiveness of the FDA 510(k) Clearance Process
Publisher : National Academies Press
Page : 318 pages
File Size : 42,9 Mb
Release : 2011-10-25
Category : Medical
ISBN : 9780309212458
Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizations have expressed concern that the 510(k) process is neither making safe and effective devices available to patients nor promoting innovation in the medical-device industry. Several high-profile mass-media reports and consumer-protection groups have profiled recognized or potential problems with medical devices cleared through the 510(k) clearance process. The medical-device industry and some patients have asserted that the process has become too burdensome and is delaying or stalling the entry of important new medical devices to the market. At the request of the FDA, the Institute of Medicine (IOM) examined the 510(k) process. Medical Devices and the Public's Health examines the current 510(k) clearance process and whether it optimally protects patients and promotes innovation in support of public health. It also identifies legislative, regulatory, or administrative changes that will achieve the goals of the 510(k) clearance process. Medical Devices and the Public's Health recommends that the U.S. Food and Drug Administration gather the information needed to develop a new regulatory framework to replace the 35-year-old 510(k) clearance process for medical devices. According to the report, the FDA's finite resources are best invested in developing an integrated premarket and postmarket regulatory framework.
Author : National Research Council
Publisher : Legare Street Press
Page : 0 pages
File Size : 55,8 Mb
Release : 2022-10-27
Category : History
ISBN : 1015698875
This work has been selected by scholars as being culturally important, and is part of the knowledge base of civilization as we know it. This work is in the "public domain in the United States of America, and possibly other nations. Within the United States, you may freely copy and distribute this work, as no entity (individual or corporate) has a copyright on the body of the work. Scholars believe, and we concur, that this work is important enough to be preserved, reproduced, and made generally available to the public. We appreciate your support of the preservation process, and thank you for being an important part of keeping this knowledge alive and relevant.