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Author: Christopher Francis
Publisher: Francisart Productions
ISBN:
Category : Juvenile Fiction
Languages : en
Pages : 101
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Book Description
A fast-paced and exciting read for middle-grade adventure and survival buffs. The story follows a self-centered, entitled boy as he crash-lands on an island and slowly learns the importance of selflessness and altruism. Riley Pickering knows he'll be the next Sidney Crosby so it is expected everyone should cater to him, take care of his needs, and worship the ground he walks on. In addition, he has no patience for school, Science, Mme. Capretta, the French language, or following rules. However, when a Science Project goes horribly wrong, Riley finds himself in the middle of the Pacific, stranded on an island scrambling to find ways to survive. When he meets two teenagers who are in a similar predicament, he begins to question whether he accidentally landed on the island, or whether he was intentionally sent there.
Author: Christopher Francis
Publisher: Francisart Productions
ISBN:
Category : Juvenile Fiction
Languages : en
Pages : 101
Get Book Here
Book Description
A fast-paced and exciting read for middle-grade adventure and survival buffs. The story follows a self-centered, entitled boy as he crash-lands on an island and slowly learns the importance of selflessness and altruism. Riley Pickering knows he'll be the next Sidney Crosby so it is expected everyone should cater to him, take care of his needs, and worship the ground he walks on. In addition, he has no patience for school, Science, Mme. Capretta, the French language, or following rules. However, when a Science Project goes horribly wrong, Riley finds himself in the middle of the Pacific, stranded on an island scrambling to find ways to survive. When he meets two teenagers who are in a similar predicament, he begins to question whether he accidentally landed on the island, or whether he was intentionally sent there.
Author: Thomas Dixon
Publisher:
ISBN:
Category : History
Languages : en
Pages : 448
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Book Description
This volume explores how Victorian philosophers, scientists, clergymen, and novelists debated the meaning of the new term 'altruism'. Including a reappraisal of Charles Darwin's ideas and insights into the rise of popular socialism, this study is highly relevant to contemporary debates about altruism, evolution, religion, and ethics.
Author: Patricia M. Tereskerz
Publisher: John Wiley & Sons
ISBN: 1405195673
Category : Medical
Languages : en
Pages : 295
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Book Description
This book provides a comprehensive resource for medical professionals on the various legal aspects involved in conducting clinical research. It encompasses legal and ethical issues such as duty of care, research malpractice and negligence, standards of care, informed consent, liability issues for Institutional Review Boards (IRB), conflicts of interest, insider trading and the disclosure and withholding of clinical trial results. It will also provide legal guidance on research contracts, setting up clinical trials and common legal pitfalls encountered in medical research.
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 030910078X
Category : Medical
Languages : en
Pages : 124
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Book Description
To improve public confidence in clinical research, a number of public and private groups have called for a publicly accessible, comprehensive, and transparent registry of relevant information on clinical trials for drugs and biologics. The public and various entities within the medical community (health care providers, researchers, medical journal editors, pharmaceutical companies, health insurers, and regulators) have different expectations and perceived needs regarding a public clinical trial registry. The IOM Committee on Clinical Trial Registries hosted a workshop on June 27, 2005, to obtain much-needed input from members of the public, public advocate groups, and the broader community of journal editors, pharmaceutical and biotech leaders, NIH, and the FDA. Participants discussed the data elements that have been at the core of debate and commented on issues of compliance and implementation of a national clinical trial registry. Developing a National Registry of Pharmacologic and Biologic Clinical Trials: Workshop Report inlcudes discussions at the workshop centered on the following five concepts, and are described within this report: 1) Purpose, 2) Which Trials to Include, 3) Delayed Disclosure Mechanism, 4) Reporting Results of Completed Trials, and 5) Compliance.
Author: Daria Kim
Publisher: Springer Nature
ISBN: 3030867781
Category : Law
Languages : en
Pages : 310
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Book Description
This book draws a unique perspective on the regulation of access to clinical trial data as a case on research and knowledge externalities. Notwithstanding numerous potential benefits for medical research and public health, many jurisdictions have struggled to ensure access to clinical trial data, even at the level of the trial results. Pro-access policy initiatives have been strongly opposed by research-based drug companies arguing that mandatory data disclosure impedes their innovation incentives. Conventionally, access to test data has been approached from the perspective of transparency and research ethics. The book offers a complementary view and considers access to individual patient-level trial data for exploratory analysis as a matter of research and innovation policy. Such approach appears to be especially relevant in the data-driven economy where digital data constitutes a valuable economic resource. The study seeks to define how the rules of access to clinical trial data should be designed to reconcile the policy objectives of leveraging the research potential of data through secondary analysis, on the one hand, and protecting economic incentives of research-based drug companies, on the other hand. Overall, it is argued that the mainstream innovation-based justification for exclusive control over the outcomes of research and development can hardly rationalise trial sponsors’ control over primary data from trials. Instead, access to such data and its robust analysis should be prioritised.
Author: Daniel Strech
Publisher: Springer
ISBN: 3319287311
Category : Philosophy
Languages : en
Pages : 223
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Book Description
In this book, scholars with different disciplinary and national backgrounds argue for possible answers and analyse case studies on current issues of governance in biomedical research. These issues comprise among others the research-care distinction, risk evaluation in early human trials, handling of incidental findings, nocebo effects, cluster randomized trials, publication bias, or consent in biobank research. This book demonstrates how new technologies and research possibilities multiply or intensify already known governance challenges, leaving room for ethical analysis and complex moral choices. Clinical researchers, research ethics committee members and research ethicists have all to deal with such challenges on a daily basis. While general reflection on core concepts of research ethics is seldom pointless, those confronted with hard moral choices do need more practical and contextualized reflection on the said issues. This book particularly provides such contextualized reflections and aims to inform all those who study, conduct, regulate, fund, or participate in biomedical research.
Author: Evan DeRenzo
Publisher: Academic Press
ISBN: 0123869358
Category : Medical
Languages : en
Pages : 368
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Book Description
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
Author: Ezekiel J. Emanuel
Publisher: OUP USA
ISBN: 0199768633
Category : Medical
Languages : en
Pages : 848
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Book Description
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.
Author: MaryAnn Foote
Publisher: Springer Science & Business Media
ISBN: 3764375833
Category : Medical
Languages : en
Pages : 202
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Book Description
ICMJE editors and other journal editors require registration of clinical trial information on publicly available Web sites before enrollment of study subjects. Not only does this book discuss the genesis of these requirements, it also provides practical information for researchers and sponsors on how to establish a workflow for a clinical registry project, how to file to a registry, and how to post results.
Author: Edward J. Huth
Publisher: ACP Press
ISBN: 1930513674
Category : Health & Fitness
Languages : en
Pages : 597
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Book Description
Who was the first to write about a certain disease, diagnose it, and treat it? This book answers those questions for a wide range of diseases, from Abetalipoproteinemia to Zollinger-Ellison syndrome. What were the medical practitioners of previous generations hoping to achieve? What were their patients expecting of them? The answers are found in these quotations. Containing over 3,000 entries, and now updated with more than 450 new quotations, this new edition of ""Medicine in Quotations"" is the most comprehensive collection of its type published in over 30 years. It is much more than a random collection of famous sayings relating to sickness and health, disease and treatment; it is a portrait of medicine throughout recorded history. You will discover how medical concepts and practices have developed and shifted through the millennia, and how many illnesses recognized today were first identified a thousand or more years ago. Quotations are organized by topic, and each is fully referenced, allowing curious readers to return to the original source. Subject and author indices make it easy to find quotations of interest. ""Medicine in Quotations"" is an invaluable resource for writers, speakers, and all those interested in the history of medicine.
