The International Declaration on Human Genetic Data is the second instrument created by the International Bioethics Committee in 2003 to extend the 1997 declaration. This document sets out a number of rules for collecting, using and storing data human genetics. It concerns, inter alia, informed consent in genetics; the confidentiality of genetic data; genetic discrimination; the anonymity of personal genetic information; genetic studies on populations; the right not to know his own genetic composition, international solidarity in genetic research, and the distribution of benefits. Notemodify wikitesto

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