The WMDA has set up a central global reporting system for WMDA member organisations to report Serious (Product) Events and Adverse Reactions – S(P)EARs – to the WMDA.
Aaim
- To gain insight in the occurrence of serious events and adverse effects in relation to blood stem cell donation by unrelated donors and blood stem cell collection/processing from unrelated donors.
Purpose
To collect and analyze information on recipient and donor serious adverse events (SAE) and reactions which affect donors and/or products from all WMDA stem cell
donor registries and cord blood banks.To follow a rapid alert system for disseminating information on SAE/R to all members of the international community in contact with allogeneic donors and patients.
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