Results of the Inquiry and Citation Review
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3.1 Genotype information
3.1.2 Disclosure of test results
3.2.2 Legal status and storage of samples and data in a biobank
3.2.3 Access to the biobank, ownership and exchange of samples
3.3.2 Information that has to be provided to the participant
3.3.3 Extended storage, secondary use of samples
3.3.5 Treatment of vulnerable subjects
3.4 The role of Ethics Committees