The idea for this manual came from Pfizer in the US, which provided the Clinical Trials Centre at The University of Hong Kong, Hong Kong SAR, PR China with a nonbinding grant for its development. "Comprising more than 500 entries, the Encyclopedia of Research Design explains how to make decisions about research design, undertake research projects in an ethical manner, interpret and draw valid inferences from data, and evaluate ... A useful resource for critical common sense in everyday life, the text provides an effective examination of a society increasingly influenced by the rhetoric of health and medicine. The aim of this book is to provide research ethics committee members with a resource that focuses on research ethics issues in Africa. Ross presents a critical investigation of the development of policy governing the involvement of children in medical research. Over the decade it took to uncover this story, Rebecca became enmeshed in the lives of the Lacks familyâespecially Henriettaâs daughter Deborah. Deborah was consumed with questions: Had scientists cloned her mother? The MacCAT-CR provides a structured format for capacity assessment that is adaptable to the particulars of any given research project. This book is also a key resource for medical students, postgraduate research students, practicing attorneys and counselors for teaching hospitals and institutions undertaking clinical research and contract research organizations. Found insideThe 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 ... Informed consent (Medical law). Informed consent - as an ethical ideal and legal doctrine - has been the source of much concern to clinicians. Kennth Getz takes a fresh look at why participation in clinical research really matters. This book addresses what clinical participation means and how it helps to advance medical science. Various mishaps have happened in recent history, and an extensive set of international rules and regulations have emerged.This book gives a thorough survey of the ethical and legal aspects of clinical research and provides a detailed ... Found inside â Page 1Informed Consent and Health Literacy is the summary of the presentations and discussion of the workshop. Found inside â Page 54INFORMED CONSENT Informed consent for a clinical trial consists of two parts: a signed document and the process of obtaining consent. The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Found insideThis enlarged edition of 'Tearoom Trade' includes the original text, together with a retrospect, written by Nicholas von Hoffman, Irving Louis Horowitz, Lee Rainwater, Donald P. Warwick, and Myron Glazer. This unique book offers a practical description of the principles of informed consent and their application in daily clinical practice. Found insideSome conferences produce proceedings, others an inspiration to labor, which finally leads to a published work. Such has been the case with regard to this volume. Found inside â Page 919,41 In many clinical trial settings , though , true informed consent can be obtained . so Sometimes , during a trial , important information derives from ... Found insideThis book Clinical Trials in Vulnerable Populations has 12 chapters divided into 4 sections: Minority Patients, Women, Medically Compromised Patients and Clinical Trials. There is a gap between what is desired - where medical care is provided solely based on high quality evidence - and the reality - where there is limited capacity to generate timely and practical evidence for drug development and to support ... In addition to the highest priority recommendations, the book offers more detailed recommendations on the conduct of clinical trials and techniques for analysis of trial data. This Userâs Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. Found insideThe Handbook of Applied Communication Research addresses a wide array of contemporary communication issues, their research implications in various contexts, and the challenges and opportunities for using communication to manage problems. A vital resource for those who are considering enrolling in a clinical trial, or for the parents, friends, or relatives of those involved in a clinical trial, this book takes away the mystery and allows the participant to enter a clinical ... 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. Found insideThis book will be of interest to stakeholders across the spectrum of research-from funders, to researchers, to journals, to physicians, and ultimately, to patients. The workshop, summarized in this volume, laid the foundation for a broader initiative of the Forum addressing different aspects of clinical research. This is a comprehensive discussion of the ethical issues involved in informing patients on their rights and participation in medical research and treatment. This is a serious omission. Experts have overlooked ethical issues that matter to subjects. Silent Partners moves subjects to the forefront, giving them a voice in research ethics. "In the new 2016 version of the ethical guidelines, CIOMS provides answers to a number of pressing issues in research ethics. Issues addressed in the book include the need for in-depth, complimentary reviews of science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal and ... I. Defining "research"--II. Issues in study design . 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. Adding to the attraction of collecting biospecimens but also to the complexity of sharing and protecting the data is the fact that this is an era of incredibly rapid gains in our understanding of complex biological and physiological ... This book examines the inadequacies of consent for contemporary biomedical research, including perspectives from medicine, law, philosophy and sociology. This evaluation included the review of documents pertaining to investigational new drug submissions, protocols and consent forms from other clinical trials, as well as information available from other clinical and preclinical experience ... Found insideProfessionals in need of such training and bioethicists will be interested. Found inside â Page iIncreasingly over the past five years, uncertainty about reimbursement for routine patient care has been suspected as contributing to problems enrolling people in clinical trials. This text aims to be a one-stop source for guidance and checking the rules for proper conduct of clinical trials, as well as providing a historical perspective of the clinical research landscape. 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