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Acceptable Risk in Biomedical Research

Език Английски езикАнглийски език
Книга С твърди корици
Книга Acceptable Risk in Biomedical Research Sigmund Simonsen
Код Либристо: 01979164
Издателство Springer, януари 2012
The book is the first major work that addresses a core question in biomedical research: the question... Цялото описание
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252.84 лв
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The book is the first major work that addresses a core question in biomedical research: the question of acceptable risk. The acceptable level of risks is regulated by the requirement of proportionality in biomedical research law, which state that the risk and burden to the participant must be in proportion to potential benefits to the participant, society or science. §This investigation addresses research on healthy volunteers, children, vulnerable subjects, and includes placebo controlled clinical trials. It represents a major contribution towards clarifying the most central, but also the most controversial and complex issue in biomedical research law and bioethics. The EU Clinical Trial Directive, the Council of Europe s Oviedo Convention (and its Additional Protocol), and national regulation in member states are covered. It is a relevant work for lawyers and ethicists, and the practical approach makes a valuable tool for researchers and members of research ethics committees supervising biomedical research.The book is the first major work that addresses a core question in biomedical research: the question of acceptable risk. The acceptable level of risks is regulated by the requirement of proportionality in biomedical research law, which state that the risk and burden to the participant must be in proportion to potential benefits to the participant, society or science. §This investigation addresses research on healthy volunteers, children, vulnerable subjects, and includes placebo controlled clinical trials. It represents a major contribution towards clarifying the most central, but also the most controversial and complex issue in biomedical research law and bioethics. The EU Clinical Trial Directive, the Council of Europe s Oviedo Convention (and its Additional Protocol), and national regulation in member states are covered. It is a relevant work for lawyers and ethicists, and the practical approach makes a valuable tool for researchers and members of research ethics committees supervising biomedical research.

Информация за книгата

Пълно заглавие Acceptable Risk in Biomedical Research
Автор Sigmund Simonsen
Език Английски език
Корици Книга - С твърди корици
Дата на издаване 2012
Брой страници 296
Баркод 9789400726772
ISBN 9400726775
Код Либристо 01979164
Издателство Springer
Тегло 635
Размери 155 x 235 x 21
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