An ethnographic exploration of research ethics committees in the UK, which highlights the central role of trust in biomedical regulatory decision making.
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Adam Hedgecoe is a Professor in the School of Social Sciences at Cardiff University -- .
Based on extensive observations, interviews, and archival research, this book provides an in-depth insight into one of the most crucial forms of regulation around medical research: Research Ethics Committees.
Every month, groups of people from all over the United Kingdom decide what kind of research should be carried out on patients within the National Health Service. These groups – Research Ethics Committees (RECs) – made up of doctors, nurses, researchers, and members of the general public – help shape the future of medicine, and play a crucial role in the regulation of a wide range of research from social science to epidemiology, vaccine and drugs trials, and surgery. Providing one of the first empirical examinations of this kind of regulation, this book highlights how, despite the trappings of a modern regulatory system, REC decision making revolves around outdated aspects of social life. Hedgecoe argues that an accurate understanding of this kind of regulation requires an acceptance of the inherently social nature of the processes involved.
In placing trust at the centre of ethics decision making, this book challenges the impersonal, de-socialised, and mechanical models of REC decision making that dominate mainstream accounts, and documents the subtle, messy, and complex way in which these bodies decide what kind of research should take place.
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Hardcover. Condición: new. Hardcover. This book focuses on Research Ethics Committees (RECs), a way of regulating research involving humans, found all across the developed world (in the US they are known as IRBs, Institutional Review Boards) and increasingly in developing countries. These bodies regulate research in advance of it taking place, by deciding whether scientists should carry out particular experiments or not. Despite coming into existence in the late 1960s, and the considerable literature bemoaning the chilling effect such review has on biomedical research and the costs and challenges associated with getting approval - we don't know very much about how these bodies make decisions. Sitting on the border between Science and Technology Studies and medical sociology, this book provides one of the first empirical examinations of this kind of regulation, drawing on observational, interview and archival data to give in-depth ethnographic insight into RECs. -- . An ethnographic exploration of research ethics committees in the UK, which highlights the central role of trust in biomedical regulatory decision making. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Nº de ref. del artículo: 9781526152916
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Hardback. Condición: New. Every month, groups of people from all over the United Kingdom decide what kind of research should be carried out on patients within the NHS. These groups - Research Ethics Committees (RECs) - made up of doctors, nurses, researchers, and members of the general public - help shape the future of medicine, and play a crucial role in the regulation of a wide range of research from social science to epidemiology, vaccine and drugs trials to surgery. Based on extensive observations, interviews, and archival research, this book provides an in-depth insight into RECs, one of the most crucial forms of regulation around medical research. In providing one of the first empirical examinations of this kind of regulation, this book challenges the impersonal, de-socialised, and mechanical models of REC decision-making. Nº de ref. del artículo: LU-9781526152916
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