Legislative History of Radiation Control of Health and Safety Act of 1968., Mar. 1975 PDF Download
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Author: United States. Bureau of Radiological Health
Publisher:
ISBN:
Category : Radiation
Languages : en
Pages : 876
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Book Description
Author: United States. Bureau of Radiological Health
Publisher:
ISBN:
Category : Radiation
Languages : en
Pages : 876
Get Book Here
Book Description
Author: United States. Bureau of Radiological Health
Publisher:
ISBN:
Category : Consumers
Languages : en
Pages : 656
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Book Description
Author: United States. Bureau of Radiological Health
Publisher:
ISBN:
Category : Consumers
Languages : en
Pages : 876
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Book Description
Author:
Publisher: DIANE Publishing
ISBN: 1428949755
Category : Cell phones
Languages : en
Pages : 42
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Book Description
The United States General Accounting Office (GAO) presents the full text of a report entitled "Telecommunications: Research and Regulatory Efforts on Mobile Phone Health Issues," published in May 2001. The report discusses the possibility of adverse health effects from radio frequency energy emitted from mobile telephones.
Author: United States. Committee on Federal Research into the Biological Effects of Ionizing Radiation
Publisher:
ISBN:
Category : Ionizing radiation
Languages : en
Pages : 474
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Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 468
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Book Description
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309175674
Category : Medical
Languages : en
Pages : 321
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Book Description
Does radiation medicine need more regulation or simply better-coordinated regulation? This book addresses this and other questions of critical importance to public health and safety. The issues involved are high on the nation's agenda: the impact of radiation on public safety, the balance between federal and state authority, and the cost-benefit ratio of regulation. Although incidents of misadministration are rare, a case in Pennsylvania resulting in the death of a patient and the inadvertent exposure of others to a high dose of radiation drew attention to issues concerning the regulation of ionizing radiation in medicine and the need to examine current regulatory practices. Written at the request from the Nuclear Regulatory Commission (NRC), Radiation in Medicine reviews the regulation of ionizing radiation in medicine, focusing on the NRC's Medical Use Program, which governs the use of reactor-generated byproduct materials. The committee recommends immediate action on enforcement and provides longer term proposals for reform of the regulatory system. The volume covers: Sources of radiation and their use in medicine. Levels of risk to patients, workers, and the public. Current roles of the Nuclear Regulatory Commission, other federal agencies, and states. Criticisms from the regulated community. The committee explores alternative regulatory structures for radiation medicine and explains the rationale for the option it recommends in this volume. Based on extensive research, input from the regulated community, and the collaborative efforts of experts from a range of disciplines, Radiation in Medicine will be an important resource for federal and state policymakers and regulators, health professionals involved in radiation treatment, developers and producers of radiation equipment, insurance providers, and concerned laypersons.
Author: United States. Congress
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 1396
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Book Description
The Congressional Record is the official record of the proceedings and debates of the United States Congress. It is published daily when Congress is in session. The Congressional Record began publication in 1873. Debates for sessions prior to 1873 are recorded in The Debates and Proceedings in the Congress of the United States (1789-1824), the Register of Debates in Congress (1824-1837), and the Congressional Globe (1833-1873)
Author: Jeffrey A. Bakal
Publisher: Elsevier
ISBN: 0323884245
Category : Science
Languages : en
Pages : 736
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Book Description
Translational Radiation Oncology covers the principles of evidence-based medicine and applies them to the design of translational research. The book provides valuable discussions on the critical appraisal of published studies and recent developments in radiation oncology, allowing readers to learn how to evaluate the quality of such studies with respect to measuring outcomes and make effective use of all types of evidence. By reading this book, researchers have access to a practical approach to help them navigate challenging considerations in study design and implementation. It is a valuable resource for researchers, oncologists and members of biomedical field who want to understand more about translational research applied to the field of radiation oncology. Translational medicine serves as an indispensable tool in grant writing and funding efforts, so understanding how to apply its principles to research is necessary to guarantee that results will be impactful to patients. - Provides a clear process for understanding, designing, executing and analyzing clinical and translational research - Presents practical, step-by-step guidance to help readers take ideas from the lab to the bedside - Written by a team of oncologists, radiologists and clinical research experts that fully cover translational research in radiation oncology
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309212421
Category : Medical
Languages : en
Pages : 318
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Book Description
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.
