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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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樓主: mountebank
41#
發(fā)表于 2025-3-28 15:42:48 | 只看該作者
42#
發(fā)表于 2025-3-28 22:27:18 | 只看該作者
Swedensubjects for that matter. The general healthcare legislation is often applicable to situations related to biomedical research and there are special acts on clinical testing of drugs and medical-technical equipment, taking biological material for research purposes and protection of sensitive informat
43#
發(fā)表于 2025-3-29 00:21:11 | 只看該作者
Switzerlandied by analogy in most clinical studies refers, among others, to Directives 93/42/EEC and 90/385/EEC which both state that clinical investigation must be carried out in accordance with the Declaration of Helsinki. There is also reference to the Declaration of Helsinki in the Guidelines on experiment
44#
發(fā)表于 2025-3-29 05:48:05 | 只看該作者
International Aspectscal research. This resulted in several treaties, resolutions, guidelinses and other international documents containing prvoisions, which aimed at protecting either directly or indirectly the position of the human test subject.
45#
發(fā)表于 2025-3-29 09:49:24 | 只看該作者
Alternatives to Full Proof of Causation the harm, there is quite some disparity when it comes to finetune the requirement of causation, particularly in certain cases where the .-requirement. appears to bring about unsatisfactory results. Even the application of the test itself is not always uniform — the range of possible variations goes
46#
發(fā)表于 2025-3-29 13:17:22 | 只看該作者
Summaries of the Country Reportsls should be carried out.. While the Helsinki Declaration therefore might appear to be formally binding due to that reference, the Belgian reporters warn not to overestimate the consequences thereof, which are already limited in light of the restricted overall scope of said Decree., Even without suc
47#
發(fā)表于 2025-3-29 19:35:28 | 只看該作者
48#
發(fā)表于 2025-3-29 22:40:52 | 只看該作者
49#
發(fā)表于 2025-3-30 02:33:31 | 只看該作者
Germanye in weiten Teilen v?llig umgestaltet und auch das Medizinproduktegesetz sowie die Strahlenschutzverordnung wurden ma?geblich reformiert. Hinzugetreten sind zum 1. August 2002 weitere ma?gebliche ?nderungen im Schadensersatzrecht und im Arzneimittelgesetz. Der nachfolgende Bericht beruht auf dem Gesetzes- und Literaturstand vom 1. August 2002.
50#
發(fā)表于 2025-3-30 07:18:34 | 只看該作者
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