The Oxford Textbook Of Clinical Research Ethics

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The Oxford Textbook of Clinical Research Ethics

Author : Ezekiel J. Emanuel
Publisher : OUP USA
ISBN 13 : 0199768633
Total Pages : 848 pages
Book Rating : 4.1/5 (997 download)

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Book Synopsis The Oxford Textbook of Clinical Research Ethics by : Ezekiel J. Emanuel

Download or read book The Oxford Textbook of Clinical Research Ethics written by Ezekiel J. Emanuel and published by OUP USA. This book was released on 2011-02 with total page 848 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Oxford Textbook of Clinical Research Ethics is the first comprehensive and systematic reference on clinical research ethics. Under the editorship of experts from the U.S. National Institutes of Health of the United States, the book's 73 chapters offer a wide-ranging and systematic examination of all aspects of research with human beings. Considering the historical triumphs of research as well as its tragedies, the textbook provides a framework for analyzing the ethical aspects of research studies with human beings. Through both conceptual analysis and systematic reviews of empirical data, the contributors examine issues ranging from scientific validity, fair subject selection, risk benefit ratio, independent review, and informed consent to focused consideration of international research ethics, conflicts of interests, and other aspects of responsible conduct of research. The editors of The Oxford Textbook of Clinical Research Ethics offer a work that critically assesses and advances scholarship in the field of human subjects research. Comprehensive in scope and depth, this book will be a crucial resource for researchers in the medical sciences, as well as teachers and students.

Rethinking the Ethics of Clinical Research

Author : Alan Wertheimer
Publisher : Oxford University Press
ISBN 13 : 0199743517
Total Pages : 369 pages
Book Rating : 4.1/5 (997 download)

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Book Synopsis Rethinking the Ethics of Clinical Research by : Alan Wertheimer

Download or read book Rethinking the Ethics of Clinical Research written by Alan Wertheimer and published by Oxford University Press. This book was released on 2011 with total page 369 pages. Available in PDF, EPUB and Kindle. Book excerpt: Introduction -- Facing up to paternalism in research ethics -- Preface to a theory of consent transactions in research : beyond valid consent -- Should we worry about money? -- Exploitation in clinical research -- The interaction principle.

Research Ethics

Author : Ana Smith Iltis
Publisher : Routledge
ISBN 13 : 1135991499
Total Pages : 232 pages
Book Rating : 4.1/5 (359 download)

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Book Synopsis Research Ethics by : Ana Smith Iltis

Download or read book Research Ethics written by Ana Smith Iltis and published by Routledge. This book was released on 2006-01-16 with total page 232 pages. Available in PDF, EPUB and Kindle. Book excerpt: Medicine in the twenty-first century is increasingly reliant on research to guarantee the safety and efficacy of medical interventions. As a result, the need to understand the ethical issues that research generates is becoming essential. This volume introduces the principal areas of concern in research on human subjects, offering a framework for understanding research ethics, and the relationship between ethics and compliance. Research Ethics brings together leading scholars in bioethics and the topics covered include the unique concerns that arise in specific areas of research such as gene therapy and stem cell research. Individual chapters also address the ethical issues that occur when conducting research with specific populations such as infants or adolescents, and the volume looks at important emerging questions in human subjects research, namely financial conflicts of interest and the interpretation of scientific data.

The Oxford Handbook of Public Health Ethics

Author : Anna C. Mastroianni
Publisher : Oxford University Press
ISBN 13 : 0190245212
Total Pages : 992 pages
Book Rating : 4.1/5 (92 download)

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Book Synopsis The Oxford Handbook of Public Health Ethics by : Anna C. Mastroianni

Download or read book The Oxford Handbook of Public Health Ethics written by Anna C. Mastroianni and published by Oxford University Press. This book was released on 2019-07-23 with total page 992 pages. Available in PDF, EPUB and Kindle. Book excerpt: Natural disasters and cholera outbreaks. Ebola, SARS, and concerns over pandemic flu. HIV and AIDS. E. coli outbreaks from contaminated produce and fast foods. Threats of bioterrorism. Contamination of compounded drugs. Vaccination refusals and outbreaks of preventable diseases. These are just some of the headlines from the last 30-plus years highlighting the essential roles and responsibilities of public health, all of which come with ethical issues and the responsibilities they create. Public health has achieved extraordinary successes. And yet these successes also bring with them ethical tension. Not all public health successes are equally distributed in the population; extraordinary health disparities between rich and poor still exist. The most successful public health programs sometimes rely on policies that, while improving public health conditions, also limit individual rights. Public health practitioners and policymakers face these and other questions of ethics routinely in their work, and they must navigate their sometimes competing responsibilities to the health of the public with other important societal values such as privacy, autonomy, and prevailing cultural norms. This Oxford Handbook provides a sweeping and comprehensive review of the current state of public health ethics, addressing these and numerous other questions. Taking account of the wide range of topics under the umbrella of public health and the ethical issues raised by them, this volume is organized into fifteen sections. It begins with two sections that discuss the conceptual foundations, ethical tensions, and ethical frameworks of and for public health and how public health does its work. The thirteen sections that follow examine the application of public health ethics considerations and approaches across a broad range of public health topics. While chapters are organized into topical sections, each chapter is designed to serve as a standalone contribution. The book includes 73 chapters covering many topics from varying perspectives, a recognition of the diversity of the issues that define public health ethics in the U.S. and globally. This Handbook is an authoritative and indispensable guide to the state of public health ethics today.

The Ethical Challenges of Human Research

Author : Franklin G. Miller
Publisher : Oxford University Press
ISBN 13 : 0199896208
Total Pages : 347 pages
Book Rating : 4.1/5 (998 download)

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Book Synopsis The Ethical Challenges of Human Research by : Franklin G. Miller

Download or read book The Ethical Challenges of Human Research written by Franklin G. Miller and published by Oxford University Press. This book was released on 2012-11-15 with total page 347 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book contains 22 essays on the ethics of research involving human subjects written over a 15-year period. Topics addressed include the ethics of clinical trials, controversial study designs, and informed consent.

Ethical Issues in Clinical Research

Author : Bernard Lo
Publisher : Lippincott Williams & Wilkins
ISBN 13 : 1451152779
Total Pages : 302 pages
Book Rating : 4.4/5 (511 download)

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Book Synopsis Ethical Issues in Clinical Research by : Bernard Lo

Download or read book Ethical Issues in Clinical Research written by Bernard Lo and published by Lippincott Williams & Wilkins. This book was released on 2012-03-28 with total page 302 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book teaches researchers how to resolve the ethical dilemmas that can arise at any stage in clinical research. In addition to explaining pertinent regulations and laws, Dr. Lo helps investigators understand the gaps and uncertainties in regulations, as well as situations in which merely complying with the law may not fulfill ethical responsibilities. Most chapters include real-life examples that the author walks through, discussing the salient issues and how to approach them. This book can be used in courses on research ethics that are required or encouraged by major National Institutes of Health grants in academic health centers.

Research Ethics Consultation

Author : Marion Danis
Publisher : OUP USA
ISBN 13 : 0199798036
Total Pages : 274 pages
Book Rating : 4.1/5 (997 download)

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Book Synopsis Research Ethics Consultation by : Marion Danis

Download or read book Research Ethics Consultation written by Marion Danis and published by OUP USA. This book was released on 2012-04-18 with total page 274 pages. Available in PDF, EPUB and Kindle. Book excerpt: The National Institutes of Health Clinical Center's Bioethics Consultation Service draws on a decade of experience to share a collection of their most interesting and informative research ethics consultations. The result is insight into the ethical issues that arise in clinical research and the practice of research ethics consultation.

Oxford Handbook of Clinical and Healthcare Research

Author : Sumantra Ray
Publisher : Oxford University Press
ISBN 13 : 0191502952
Total Pages : 640 pages
Book Rating : 4.1/5 (915 download)

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Book Synopsis Oxford Handbook of Clinical and Healthcare Research by : Sumantra Ray

Download or read book Oxford Handbook of Clinical and Healthcare Research written by Sumantra Ray and published by Oxford University Press. This book was released on 2016-03-03 with total page 640 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Oxford Handbook of Clinical and Healthcare Research is a practical, concise, and easy-to-use reference for the full range of clinical and healthcare research topics, while incorporating evidence based medicine. Comprehensively providing a wide breadth of knowledge, this handbook clearly covers both the qualitative and quantitative aspects. This handbook includes clear instructions on the legislative requirements as well as the practical requirements of commissioning, conducting, analysing, and reporting research for those in clinical or healthcare practice, education or training. This book has been written with Good Clinical Practice (GCP) education in mind, giving valuable information needed for the accredited certificates and diploma-level benchmark exams now commonly required by employers. Whether you need practical advice on setting up and running a trial, negotiating regulations, learning vital research skills, or to study the underpinning concepts of research methods, this handbook will give you the vital information, clinical evidence, and guidance you need.

Silent Partners

Author : Rebecca Dresser
Publisher : Oxford University Press
ISBN 13 : 0190459298
Total Pages : 208 pages
Book Rating : 4.1/5 (94 download)

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Book Synopsis Silent Partners by : Rebecca Dresser

Download or read book Silent Partners written by Rebecca Dresser and published by Oxford University Press. This book was released on 2016-10-03 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt: When is a human study ethical? For years, science and society have struggled with this question. Experts have put great effort into developing ethical principles and rules that adequately protect and respect volunteers in studies aimed at improving human health. But experts have missed something important. They have created a research ethics system without the help of people who know what it is like to be a research subject. This is a serious omission. Experienced research subjects can make valuable contributions to research ethics. People who have been in studies have information about the experience that other people can overlook. Their experience as subjects gives them special insights into ethics, too. Experienced subjects also know about problems that can lead people to refuse to join studies, or drop out before studies are complete. Scientists and ethicists often speak of subjects as partners in research, but the reality is quite different. Experienced subjects are rarely appointed to the advisory groups that create guidelines for ethical research, or to the committees that review individual studies to determine whether they meet ethical and regulatory standards. A large body of work describes the perceptions and viewpoints of people who have participated in research. But experts rarely use this material to guide improvements in human subject protection. Although subjects have the power to decide whether to participate in a study, they have little control over anything else that goes on in research. Silent Partners moves research subjects to the forefront. It examines what research participation is like for healthy volunteers and patients. It explains why subjects' voices should influence research ethics. Silent Partners shows how experienced research subjects can become real-not just symbolic-partners in research.

Ethical Considerations When Preparing a Clinical Research Protocol

Author : Evan DeRenzo
Publisher : Academic Press
ISBN 13 : 0123869544
Total Pages : 370 pages
Book Rating : 4.1/5 (238 download)

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Book Synopsis Ethical Considerations When Preparing a Clinical Research Protocol by : Evan DeRenzo

Download or read book Ethical Considerations When Preparing a Clinical Research Protocol written by Evan DeRenzo and published by Academic Press. This book was released on 2020-06-12 with total page 370 pages. Available in PDF, EPUB and Kindle. Book excerpt: Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and assent documents, how to get protocols approved, special populations, confidentiality issues, and the reporting of adverse events. The book's valuable appendix includes a listing of web resources about research ethics, along with a glossary, making it an invaluable resource for scientists collaborating in clinical trials, physician investigators, clinical research fellows, and more. Walks investigators and trainees through the identification of the ethical aspects of each section of a clinical research protocol Includes case histories that illustrate key points Contains information on conducting clinical research within the pharmaceutical industry Includes internet resources and worldwide web addresses for important research ethics documents and regulations Contains a chapter on Study Design and Methodology that is purposely expanded to explicitly address biostatistical considerations

Research Ethics Consultation

Author : Emily Largent
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (794 download)

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Book Synopsis Research Ethics Consultation by : Emily Largent

Download or read book Research Ethics Consultation written by Emily Largent and published by . This book was released on with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Interesting and important ethical questions confront researchers, regulators, institutional review boards, support personnel, and research participants committed to the ethical conduct of human subjects research at all stages of research. Questions encompass - but are not limited to - study design, enrolling participants, balancing the clinical needs of participants against the research agenda, ending trials, discharging post-trial obligations, and resolving conflicts. Straightforward solutions to these types of questions are often not found in regulations, ethics codes, or the bioethics literature. These resources may leave room for interpretation, offer conflicting guidance, or simply fail to address particular questions. Ethics consultation, which has been offered in clinical care settings with regularity since the 1980s, has since the turn of the century increasingly been sought in the clinical research context. Because there has only lately been recognition that ethics consultants can play a valuable role helping the research community conduct research in the most ethically informed way, there are many open questions in the field of research ethics consultation including the appropriate role of consultants and the best methods of consultation. The Clinical Center Bioethics Consultation Service has been serving the NIH community of researchers, administrators, healthcare providers, and research participants for more than a decade, conducting nearly 1,000 consultations in that time. In this book, members of the Bioethics Consultation Service reflect on this long track-record and unparalleled range of research ethics consultations to share a collection of their most interesting and informative research ethics consultations and to start a dialogue on remaining open questions. Although the NIH experience is unique, this book focuses on cases - and associated lessons - that are generalizable and valuable for the entire clinical research community. This book will be valuable to ethics consultants, clinical investigators, students and teachers, and others desiring insight into clinical research ethics and ethics consultation.

Ethics and Regulation of Clinical Research

Author : Robert J. Levine
Publisher : Yale University Press
ISBN 13 : 9780300042887
Total Pages : 484 pages
Book Rating : 4.0/5 (428 download)

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Book Synopsis Ethics and Regulation of Clinical Research by : Robert J. Levine

Download or read book Ethics and Regulation of Clinical Research written by Robert J. Levine and published by Yale University Press. This book was released on 1988-01-01 with total page 484 pages. Available in PDF, EPUB and Kindle. Book excerpt: The use of human subjects in medical and scientific research has given rise to troubling ethical questions. How should human subjects be selected for experiments? What should they be told about the research in which they are involved? How can their privacy be protected? When is it permissible to deceive them? How do we deal with subjects such as children, fetuses, and the mentally infirm, for whom informed consent is impossible? In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions. His book is an essential reference for everyone--members of institutional review boards, scientists, philosophers, lawyers--addressing the ethical issues involved. "[Levine's] experience as a clinician, IRB chairman, writer and editor of a journal devoted exclusively to issues faced by IRBS makes him uniquely qualified to bring together the legal, ethical, and practical dimensions. . . [The book] is sophisticated but readable. . . [and] should be on every IRB administrator's desk and in every medical ethics library."--Norman Fost, M.D., The New England Journal of Medicine "Levine. . . is one of the foremost historians of contemporary clinical science. . . . His book is at once a guide to primary sources for the history of clinical research in the late twentieth century and a pioneering secondary source about that history."--Daniel M. Fox, Bulletin of the History of Medicine "You will be charmed by the [book's] elegance and lucidity and. . . persuaded of its relevance to doctors in any country."--Alex Paton, British Medical Journal "Should be of wide interest to those keen to see advances in medical research brought into general medical practice."--Gilbert Omenn, Issues in Science and Technology

Ethical and Regulatory Aspects of Clinical Research

Author : Ezekiel J. Emanuel
Publisher :
ISBN 13 :
Total Pages : 532 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Ethical and Regulatory Aspects of Clinical Research by : Ezekiel J. Emanuel

Download or read book Ethical and Regulatory Aspects of Clinical Research written by Ezekiel J. Emanuel and published by . This book was released on 2003 with total page 532 pages. Available in PDF, EPUB and Kindle. Book excerpt: Professionals in need of such training and bioethicists will be interested.

Medical Experimentation

Author : Charles Fried
Publisher : Oxford University Press
ISBN 13 : 0190602740
Total Pages : 176 pages
Book Rating : 4.1/5 (96 download)

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Book Synopsis Medical Experimentation by : Charles Fried

Download or read book Medical Experimentation written by Charles Fried and published by Oxford University Press. This book was released on 2016-05-02 with total page 176 pages. Available in PDF, EPUB and Kindle. Book excerpt: First published in 1974, Charles Fried's Medical Experimentation is a classic statement of the moral relationship between doctor and patient, as expressed within the concept of personal care. This concept is then tested in the context of medical experimentation and, more specifically, the randomized controlled trial (RCT). Regularly referred to as a point of departure for ethical and legal discussions of the RCT, the book has long been out of print. This new, second edition includes a general introduction by Franklin Miller and the late Alan Wertheimer, a reprint of the 1974 text, and an in-depth analysis by Harvard Law School scholars I. Glenn Cohen and D. James Greiner which discusses the extension of RTCTs to social science and public policy contexts. The volume concludes with a new essay by Charles Fried that reflects on the original text and how it applies to the contemporary landscape of medicine and medical experimentation.

Ethics in Clinical Research

Author : Dr. Jane Barrett
Publisher : Inst of Clinical Research
ISBN 13 : 1905238029
Total Pages : 76 pages
Book Rating : 4.9/5 (52 download)

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Book Synopsis Ethics in Clinical Research by : Dr. Jane Barrett

Download or read book Ethics in Clinical Research written by Dr. Jane Barrett and published by Inst of Clinical Research. This book was released on 2006 with total page 76 pages. Available in PDF, EPUB and Kindle. Book excerpt: Until recently there has been no formal law covering many aspects of clinical research, making the ethical and scientific guidelines more important. Rapidly changing law gives researchers challenges when deciding research policies. There is relatively little teaching on the ethics of clinical research and this monograph intends to trigger thought and discussion as well as provide guidance in decision-making.

Exploitation and Developing Countries

Author : Jennifer S. Hawkins
Publisher : Princeton University Press
ISBN 13 : 0691126763
Total Pages : 337 pages
Book Rating : 4.6/5 (911 download)

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Book Synopsis Exploitation and Developing Countries by : Jennifer S. Hawkins

Download or read book Exploitation and Developing Countries written by Jennifer S. Hawkins and published by Princeton University Press. This book was released on 2008-08-24 with total page 337 pages. Available in PDF, EPUB and Kindle. Book excerpt: Introduction : Why exploitation? / Jennifer S. Hawkins and Ezekiel J. Emanuel -- Research ethics, developing countries, and exploitation : a primer / Jennifer S. Hawkins -- Case studies : the Havrix trial and the Surfaxin trial -- Exploitation in clinical research / Alan Wertheimer -- Testing our drugs on the poor abroad / Thomas Pogge -- Broadly utilitarian theories of exploitation and multinational clinical research / Richard J. Arneson -- Kantian ethics, exploitation, and multinational clinical trials / Andrew W. Siegel -- Exploitation and the enterprise of medical research / Alisa L. Carse and Margaret Olivia Little -- Exploitation and placebo controls / Jennifer S. Hawkins -- Addressing exploitation : reasonable availability versus fair benefits / Ezekiel J. Emanuel.

An Introduction to Clinical Research

Author : Piers Page
Publisher : OUP Oxford
ISBN 13 : 0191629596
Total Pages : 224 pages
Book Rating : 4.1/5 (916 download)

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Book Synopsis An Introduction to Clinical Research by : Piers Page

Download or read book An Introduction to Clinical Research written by Piers Page and published by OUP Oxford. This book was released on 2011-11-10 with total page 224 pages. Available in PDF, EPUB and Kindle. Book excerpt: This practical book is written specifically for junior doctors by a team of highly experienced authors, as an introductory guide to clinical research. It covers all areas that a junior doctor needs to consider, including funding, study design, ethics, data analysis, disseminating findings, and furthering one's research career. It presents a balance view of clinical research and is written by authors actively involved in clinical research both at the 'coal-face' and at a more supervisory level. Research can be a difficult process and it is essential to make sure that the project is set up in the correct way in order to get verifiable results. This easy-to-read guide is available to help junior doctors develop a good study design and present evidence of a sound academic practice, which will make obtaining funding more likely and be time-efficient. Getting started early in research and developing a solid, gradual understanding of clinical research through using this approachable book will be of huge benefit to junior doctors and their discipline.