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New SPEAR online reporting tool

We are very proud to announce that our new and improved version of the SPEAR online reporting tool will go live on April 4th! You can reach it on https://spear.wmda.info

If you have questions, you can always contact us at sear-spear@wmda.info.

Serious (Product) Events and Adverse Reactions - S(P)EAR

WMDA has set up a central global reporting system to report Serious (Product) Events and Adverse Reactions – S(P)EARs – to the WMDA. To access the reporting system, you login with your email address and password. If you do not have a password, contact the WMDA office

Aim

  • 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 analyse 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.

Important note!

The SPEAR Committee reviews all reported incidents once a week. If you have a rapid alert that needs to be shared with the community quickly, we urge you to send a separate e-mail to the WMDA office (sear-spear@wmda.info) or call us on: +31 88 505 7900.








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