Download Full eBooks in PDF
Compliance And Enforcement Program Book in PDF, ePub and Kindle version is available to download in english. Read online anytime anywhere directly from your device. Click on the download button below to get a free pdf file of Compliance And Enforcement Program book. This book definitely worth reading, it is an incredibly well-written.
Author : MARIO D. BELLISSIMO
Publisher : Unknown
Page : 128 pages
File Size : 50,7 Mb
Release : 2019
Category : Electronic
ISBN : 0779891368
Author : United States. Federal Aviation Administration
Publisher : Unknown
Page : 444 pages
File Size : 52,6 Mb
Release : 1988
Category : Aeronautics
ISBN : MINN:30000002710980
Author : Jennifer Arlen
Publisher : Edward Elgar Publishing
Page : 392 pages
File Size : 53,5 Mb
Release : 2018
Category : Electronic
ISBN : 9781783474479
Jennifer Arlen brings together 13 original chapters by leading scholars that examine how to deter corporate misconduct through public enforcement and private interventions. Scholars from a variety of disciplines present both theoretical and empirical analyses of organizational and individual liability for corporate crime, liability for foreign corruption, securities fraud enforcement, compliance, corporate investigations, and whistleblowing. This Research Handbook also highlights promising avenues for future research.
Author : United States. Federal Aviation Administration
Publisher : Unknown
Page : 444 pages
File Size : 46,7 Mb
Release : 1992
Category : Aeronautics
ISBN : IND:30000066283320
Author : Paddock, Lee
Publisher : Edward Elgar Publishing
Page : 212 pages
File Size : 48,7 Mb
Release : 2021-09-21
Category : Law
ISBN : 9781789902204
This Advanced Introduction provides a clear and accessible guide to the essential elements of environmental compliance and enforcement programs. It examines compliance programs designed to assist regulated entities in meeting their obligations, as well as enforcement tools designed to address non-compliance - such as administrative, civil judicial, and criminal enforcement. Offering an insightful overview of this important area, LeRoy C. Paddock highlights recent developments that are changing the way compliance and enforcement work is practiced.
Author : Anonim
Publisher : DIANE Publishing
Page : 47 pages
File Size : 50,6 Mb
Release : 2024-06-29
Category : Electronic
ISBN : 9781428965126
Author : Howard L. Dorfman
Publisher : Unknown
Page : 128 pages
File Size : 53,9 Mb
Release : 2021
Category : Drugs
ISBN : 1402438486
Author : United States. Food and Drug Administration. Division of Microbiology
Publisher : Unknown
Page : 180 pages
File Size : 49,5 Mb
Release : 1969
Category : Microbiology
ISBN : STANFORD:36105214583721
Author : Institute of Medicine,Committee on Nursing Home Regulation
Publisher : National Academies Press
Page : 432 pages
File Size : 49,7 Mb
Release : 1986-02-01
Category : Medical
ISBN : 9780309036467
As more people live longer, the need for quality long-term care for the elderly will increase dramatically. This volume examines the current system of nursing home regulations, and proposes an overhaul to better provide for those confined to such facilities. It determines the need for regulations, and concludes that the present regulatory system is inadequate, stating that what is needed is not more regulation, but better regulation. This long-anticipated study provides a wealth of useful background information, in-depth study, and discussion for nursing home administrators, students, and teachers in the health care field; professionals involved in caring for the elderly; and geriatric specialists.
Author : Canada. Competition Bureau
Publisher : Canadian Government Publishing
Page : 58 pages
File Size : 41,5 Mb
Release : 2000
Category : Intellectual property
ISBN : 066265224X
Author : United States. Office of Federal Contract Compliance Programs
Publisher : Unknown
Page : 148 pages
File Size : 45,5 Mb
Release : 1979
Category : Discrimination in employment
ISBN : UOM:39015077151853
Author : Food and Drug Administration
Publisher : Unknown
Page : 0 pages
File Size : 40,5 Mb
Release : 2003
Category : Drugs
ISBN : 0865879737
Available now to FDA-regulated organizations, this manual allows facility managers to look at their operation's regulatory compliance through the eyes of the government. Because this is the primary reference manual used by FDA personnel to conduct field investigation activities, you can feel confident you are preparing appropriate planning or action. This manual includes revised instructions regarding the release of information and covers FDA's policies and expectations on a comprehensive range of topics: FDA's authority to enter and inspect, inspection notification, detailed inspection procedures, recall monitoring, inspecting import procedures, computerized data requests, federal/state inspection relationships, discussions with management regarding privileged information, seizure and prosecution, HACCP, bioengineered food, dietary supplements, cosmetics, bioterrorism, and product disposition. The manual also includes a directory of Office of Regulatory Affairs offices and divisions.
Author : United States Accounting Office (GAO)
Publisher : Createspace Independent Publishing Platform
Page : 30 pages
File Size : 54,6 Mb
Release : 2018-05-28
Category : Electronic
ISBN : 1720425108
Observations on Compliance and Enforcement in EPA's Drinking Water Program
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 : 42,7 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 : Institute of Medicine,Board on Health Sciences Policy,Committee on Clinical Research Involving Children
Publisher : National Academies Press
Page : 445 pages
File Size : 48,8 Mb
Release : 2004-07-09
Category : Medical
ISBN : 9780309133388
In recent decades, advances in biomedical research have helped save or lengthen the lives of children around the world. With improved therapies, child and adolescent mortality rates have decreased significantly in the last half century. Despite these advances, pediatricians and others argue that children have not shared equally with adults in biomedical advances. Even though we want children to benefit from the dramatic and accelerating rate of progress in medical care that has been fueled by scientific research, we do not want to place children at risk of being harmed by participating in clinical studies. Ethical Conduct of Clinical Research Involving Children considers the necessities and challenges of this type of research and reviews the ethical and legal standards for conducting it. It also considers problems with the interpretation and application of these standards and conduct, concluding that while children should not be excluded from potentially beneficial clinical studies, some research that is ethically permissible for adults is not acceptable for children, who usually do not have the legal capacity or maturity to make informed decisions about research participation. The book looks at the need for appropriate pediatric expertise at all stages of the design, review, and conduct of a research project to effectively implement policies to protect children. It argues persuasively that a robust system for protecting human research participants in general is a necessary foundation for protecting child research participants in particular.
