Biobank Governance in Spain: From the Autonomy of Research Ethics Committees to the Autonomy of Lay People

Author:

da Rocha Antonio Casado

Publisher

Springer Netherlands

Reference19 articles.

1. Brand, A.M., and N.M. Probst-Hensch. 2007. Biobanking for epidemiological research and public health. Pathobiology 74: 227–238.

2. Casado, A. 2009. Towards a comprehensive concept of patient autonomy. The American Journal of Bioethics 9(2): 37–38.

3. Casado, A., and Etxeberria, I. 2009. Consent by research ethics committees: The new law on biomedical research in Spain. In Principles and practice in biobank governance, ed. Jane Kaye and Mark Stranger, 93–103. Farnham: Ashgate.

4. Casado, A., and J.A. Seoane. 2008. Alternative consent models for biobanks: The new Spanish law on biomedical research. Bioethics 22: 440–447.

5. CIOMS (Council for International Organizations of Medical Sciences). 2002. International ethical guidelines for biomedical research involving human subjects. Geneva: WHO. http://www.cioms.ch/frame_guidelines_nov_2002.htm .

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