Manual for Research Ethics Committees: Centre of Medical Law by Sue Eckstein PDF

By Sue Eckstein

ISBN-10: 0511550081

ISBN-13: 9780511550089

ISBN-10: 0521810043

ISBN-13: 9780521810043

ISBN-10: 1898484007

ISBN-13: 9781898484004

The 6th version of the guide for study Ethics Committees is an particular compilation of felony and moral assistance that's necessary for participants of analysis ethics committees, researchers keen on human study, contributors of the pharmaceutical and scholars of legislations, medication, ethics and philosophy. offered in a transparent and authoritative shape, it comprises the foremost criminal and moral directions. within the 6th version there are fifteen new chapters protecting key concerns, from participation in medical trials to cloning. For the 1st time, the guide is produced in a single easy-to-search hardback quantity.

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Extra info for Manual for Research Ethics Committees: Centre of Medical Law and Ethics, King's College London

Sample text

In particular they are to consider: r the relevance of the trial and the trial design r the protocol r the suitability of the investigator and supporting staff r the investigator’s brochure r the quality of the facilities r the adequacy and completeness of the written information to be given r the procedure to be used for obtaining informed consent r recruitment arrangements r the compensation provisions and insurance or indemnity arrangements r the proposed remuneration for investigators and sub- jects.

Medical Ethics Today: its Practice and Philosophy. London: BMJ Publishing Group. Davis, N. (1991). Contemporary deontology. In Companion to Ethics, ed. uk/depsta/law/research/cmle/ P. Singer, pp. 205–218. Oxford: Blackwell. Doyal, L. S. ) (2001). Informed Consent in Medical Research. London: BMJ Books. Foot, P. (1978). Virtues and Vices and Other Essays in Moral Philosophy. Oxford: Blackwell. html Freeman, B. (1987). Equipoise and the ethics of clinical research. N Eng J Med, 317, 141–145. The Hastings Center Glover, J.

None of these three regulations was well known outside Germany and Russia, whereas the responses to the Nazi concentration camp experiments became very well known. The first response was the ‘Doctors’ Trial’, starting in Nuremberg in 1946, in which 23 physicians were put on trial for crimes against humanity. Part of the judgement7 delivered by the entirely American tribunal in 1947 became known as the Nuremberg Code: it sets out ten fundamental principles for the ethical conduct of medical research, and starts with the blunt statement that ‘The voluntary consent of the human subject is absolutely essential’.

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Manual for Research Ethics Committees: Centre of Medical Law and Ethics, King's College London by Sue Eckstein


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