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Titlebook: Liability for and Insurability of Biomedical Research with Human Subjects in a Comparative Perspecti; Jos Dute,Michael G. Faure,Helmut Koz

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發(fā)表于 2025-3-21 16:43:44 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Liability for and Insurability of Biomedical Research with Human Subjects in a Comparative Perspecti
編輯Jos Dute,Michael G. Faure,Helmut Koziol
視頻videohttp://file.papertrans.cn/586/585536/585536.mp4
概述country reporters from Belgium, England, France, Germany, the Netherlands, Spain, Sweden, and Switzerland.comparative analysis completes the survey
叢書名稱Tort and Insurance Law
圖書封面Titlebook: Liability for and Insurability of Biomedical Research with Human Subjects in a Comparative Perspecti;  Jos Dute,Michael G. Faure,Helmut Koz
描述Recent Dutch legislation has been introduced stating that biomedical research on humans can only be undertaken when an insurance contract covering the damage as a result of death or personal injury of the patients has been concluded. The aim of this legislation is to ease the acquiring of compensation for test subjects in case damage arises in the course of biomedical research. As such, victims are able to claim compensation directly from the insurer, irrespective of any liability.This volume presents a critical evaluation of the functioning of this legislative arrangement and the situation in various European countries is examined. Country reporters from Belgium, England, France, Germany, the Netherlands, Spain, Sweden and Switzerland describe the insurance and liability arrangements relating to biomedical research in their country. The concluding three reports of this volume examine the situation from both a comparative and international perspective.
出版日期Book Mar 2004Latest edition
關(guān)鍵詞Belgium; England; France; Germany; Spain; Sweden; Switzerland; The Netherlands; biomedical research; case of
版次1
doihttps://doi.org/10.1007/978-3-7091-0601-3
issn_series 1616-8623
copyrightSpringer-Verlag Wien 2004
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 23:42:31 | 只看該作者
Netherlandshe interests of the researcher the institution for scientific research and the (pharmaceutical) industry. On account of structural third-party presence at biomedical research involving human subjects, protection of the test subject against (possible) injury deserves special legal attention.
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發(fā)表于 2025-3-22 15:19:45 | 只看該作者
Summaries of the Country Reportsh quotation, the Declaration seems to be a commonly accepted source of reference in Belgium when it comes to determining ethical standards. Apart from that, the 1992 Decree has failed to improve the effectiveness of such standards since it lacks, for example, statutory control mechanism.
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發(fā)表于 2025-3-23 01:09:53 | 只看該作者
Switzerlandmedic) prepared information for the Ethical Review Boards (ERB) on how the Swiss regulation should be interpreted in light of the new requirements Declaration of Helsinki, especially as to the restrictive use of placebo controlled studies.
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發(fā)表于 2025-3-23 03:20:21 | 只看該作者
Englandresearch is based on the same law, (the torts of negligence, trespass to the person (battery) requiring consent to a touching of the body, and product liability as applies to claims by patients injured in the course of routine medical treatment.
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發(fā)表于 2025-3-23 07:52:55 | 只看該作者
Francee la loi fran?aise du 20 décembre 1988 relative à protection de la pesronne qui se prête à des recherches biomédicales., la Parlement et le Conseil Européeens établissent un lien direct entre la protection de l’individu qui participe à un essai et les mécanismes qui président à son indemnisation.
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