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Donor and liability insurance of donor registries, donor centers, and collection centers – recommendations

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The article presents views and recommendations of the World Marrow Donor Association regarding the need for donor and liability insurance for hematopoietic stem cell donor registries, and donor and collection centers.

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References

  1. Goldman JM, for the Executive Committee of the World Marrow Donor Association. Special report: Bone marrow transplants using volunteer donors – recommendations and requirements for a standardized practice throughout the world – 1994 update. Blood 1994; 84: 2833–2839.

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  2. Rosenmayr A, Hartwell L, Egeland T, on behalf on the Ethics Working Group of the World Marrow Donor Association. Informed consent – suggested procedures for informed consent for unrelated haematopoietic stem cell donors at various stages of recruitment, donor evaluation, and donor workup. Bone Marrow Transplant 2003; 31: 539–545.

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  3. Bakken R, van Walraven A-M, Egeland T, for the Ethics Working Group of the World Marrow Donor Association. Donor commitment and patient needs. Bone Marrow Transplant 2003; 33: 225–230.

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Correspondence to T Egeland.

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Egeland, T., Lie, J., Persson, U. et al. Donor and liability insurance of donor registries, donor centers, and collection centers – recommendations. Bone Marrow Transplant 33, 467–470 (2004). https://doi.org/10.1038/sj.bmt.1704387

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  • DOI: https://doi.org/10.1038/sj.bmt.1704387

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