Withdrawal from Biobank Research: Considerations and the Way Forward

Author:

Hug Kristina,Hermerén Göran,Johansson Mats

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology

Reference42 articles.

1. Council of Europe. (1997). Convention for the Protection of Human Rights and Dignity of the Human Being with Regard to the Application of Biology and Medicine: Convention on Human Rights and Biomedicine. Oviedo, 4.IV [cited 2011 October 14]; Available from: URL: http://conventions.coe.int/Treaty/Commun/QueVoulezVous.asp?NT=164&CL=ENG .

2. European Parliament and Council. (2001). Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. [cited 2011 October 14]; Available from: URL: http://www.eortc.be/services/doc/clinical-eu-directive-04-april-01.pdf

3. The World Medical Association. (2008). Declaration of Helsinki 2008 [cited 2011 October 18]; Available from: URL: http://www.wma.net/e/ethicsunit/helsinki.htm .

4. Council for International Organizations of Medical Sciences (CIOMS). (2002). International Ethical Guidelines for Biomedical Research Involving Human Subjects. Commentary on Guideline 4 [cited 2011 October 12]; Available from: URL: http://www.cioms.ch/frame_guidelines_nov_2002.htm .

5. Helgesson, G., & Johnsson, L. (2005). The right to withdraw consent to research on Biobank samples. Medicine, Healthcare and Philosophy, 8(3), 315–321.

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