Acceptable Risk in Biomedical Research

European Perspectives

de

Éditeur :

Springer


Collection :

International Library of Ethics, Law, and the New Medicine

Paru le : 2012-01-04



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Description

This 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.
Pages
296 pages
Collection
International Library of Ethics, Law, and the New Medicine
Parution
2012-01-04
Marque
Springer
EAN papier
9789400726772
EAN EPUB
9789400726789

Informations sur l'ebook
Nombre pages copiables
2
Nombre pages imprimables
29
Taille du fichier
481 Ko
Prix
94,94 €