Public Trust in Medical Research?: Ethics, Law and Accountability

Front Cover
Radcliffe Publishing, 2007 - Medical - 160 pages
It has been claimed by fertility experts that embryos can be screened for 6,000 diseases, thereby the risk of x-linked diseases can be minimised by 'cherry-picking' male embryos that do not carry the abnormal gene. If medical scientists continue to strive for cures, genetic aberrance in human could be a phenomenon of the past...This challenging book explores issues of professional integrity and ethics underpinning medical research. It includes real-life case studies where public trust in medical research has been misplaced and encourages medical professionals to adhere to professional codes of conduct and be informed about their decision making process. It is vital reading for undergraduate and postgraduate students of medicine, law, sociology and social policy, philosophy, health related research and ethics. Practising researchers in medicine and the pharmaceutical industry, and their managers will find it invaluable. The text provides motivation for academics and educators with an interest in research and governance. Healthcare policy makers and shapers, patient rights groups, campaigners and the general media will find the information enlightening. "Over the last four decades, medicine has given hope to many people and saved many lives as a result of the ability of the physicians and surgeons to develop new treatments and innovative surgical techniques. While we can celebrate the success of medical science, we should also critically examine some of these developments against principles and in the light of public opinion." - Philip Cheung.
 

Contents

The role of the public in shaping progress
9
Contents
27
4
30
The Apothecaries Act 1815 and the Anatomy Act 1832
37
The Corneal Grafting Act 1952
44
Misinterpreting the rules of postmortem examination
75
Ownership of and respect for the body
89
Natural law and medical research
97
Issues of public trust
107
Ethics and the practice of informed consent
119
The medical profession and the public
131
Empowering the public
137
Creating an ethical culture in medical research
145
Postscript
151
35
155
Copyright

33
104

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