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Acceptable Risk in Biomedical Research European Perspectives /
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 pr...
| Clasificación: | Libro Electrónico |
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| Autor principal: | |
| Autor Corporativo: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Dordrecht :
Springer Netherlands : Imprint: Springer,
2012.
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| Edición: | 1st ed. 2012. |
| Colección: | International Library of Ethics, Law, and the New Medicine,
50 |
| Temas: | |
| Acceso en línea: | Texto Completo |
Tabla de Contenidos:
- 1. Introduction
- 2. Method and material
- 3. Initial conceptual clarifications
- 4. Origins of the requirement of proportionality
- 5. The purpose of the requirement of proportionality
- 6. Introduction: Part II
- 7. Which risks, burdens and potential benefits are relevant?
- 8. How to estimate risks, burdens, and potential benefits
- 9. The requirement of proportionality - initial clarifications
- 10. Therapeutic research
- 11. Nontherapeutic research
- 12. Nontherapeutic research on "vulnerable" participants
- 13. Non-interference with necessary clinical interventions and the no harm rule
- 14. Especially on randomised clinical trials, including placebo controlled clinical trials
- 15. Acceptable Risks and Burdens to Others than the Participant
- 16. Later developments during the course of the research
- 17. Legal effects of the requirement of proportionality
- 18. Summary of results
- 19. Recommendations
- 20. Perspectives
- 21. Appendix.-.