Ethics Watch (original) (raw)

Nature Reviews Genetics volume 5, page 485 (2004) Cite this article

The Council does not consider that different options need to be offered in the informed consent for use of samples obtained during medical care. Furthermore, informed consent can be waived if the samples and data are made completely anonymous, unless a prior contrary wish has been expressed.

It also recommends that “donors should be able to give generalized consent to the use of their samples and data for the purposes of medical — including genetic — research”. The same applies to the length of storage and use of the data. Neither is limited in advance.

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References

  1. German National Ethics Committee (Nationaler Ethikrat). Biobanks for Research, Opinion (German National Ethics Committee, 2004) (available in English at http://www.ethikrat.org/_english/news/next_meeting.html).

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Authors and Affiliations

  1. Bartha M. Knoppers

Authors

  1. Bartha M. Knoppers

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Knoppers, B. Ethics Watch.Nat Rev Genet 5, 485 (2004). https://doi.org/10.1038/nrg1396

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