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Protocols and Consent Forms

CIBMTR encourages centers to invite transplant recipients and donors to participate in the CIBMTR Observational Database and Research Sample Repository.

To participate, centers need to use approved CIBMTR protocols and informed consent documents for the Observational Database and the Research Sample Repository. These protocols and informed consent documents must be submitted to each center’s local IRB for review and approval.


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Last Updated: 8/20/2014 3:24 PM